WEBVTT

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And thank you for the organizers for this opportunity to discuss our work. Um, in this

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talk, uh, although I've enjoyed hearing a lot about diamonds and small scale magnetic resonance,

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this morning we're going to change topic and go to a different sensor and different length scales

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and talk maybe more about the themes of miniaturized, the size of the overall NMR

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instrument rather than the sample that we're going to study. And so that involves these types of

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sensors which are involving atomic spins, uh, atomic

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vapors of alkali metals like rubidium, cesium, etc.. If you want to know more about

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that, I can recommend that you consult this, uh, recently published review article, which was

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written by several of the people in the room Dmitri, John, James and myself and others, uh, of how

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this area, how this intersection of vapor based magnetic resonance sensing and nuclear

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spin sensing, uh, has developed. Um, and had this had this long,

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let's say, intersection over over many years, maybe approaching two decades now.

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Since I think that's unfamiliar to you, I'll give a kind of tutorial introduction to it. And then I

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want to explain more about, um, how this could go on in the future towards smaller sized

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systems. So I'll talk about, uh, small size hardware

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and samples, um, to generally increase the overall

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accessibility of these type of magnetic resonance experiments. And I'll give you an idea of some of

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the applications as well. And we work in this kind of feedback loop where when we develop some

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hardware, it leads to ideas for new experiments and keep. Keeps going. So I think that, uh, this is,

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um, a nice environment to discuss that in with many people here. Okay, so,

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uh, since I think this is unfamiliar to you, I'll show you what what an atomic magnetometer looks

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like. Um, this is the key sensor part. So this is, uh, a little box which

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contains an alkali metal. This is rubidium hanging out here, and there is some equilibrium between

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atoms in the vapor and the metal. It's oxygen free. Otherwise, the metal would simply oxidize. Uh, and

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then detecting magnetic fields involves nothing more than passing light through. Uh, so long as

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that light is resonant with the atomic transition and is is circularly polarized. So before going

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into detail of that, uh, we just see some examples here. So we could, we could either detect the

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magnetic field through the precession of the the electron valence spin in the atoms.

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Or we could detect just based on the transmission. Um, the transmission depends on magnetic field

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through a saturation effect, which you could see through the diagram. Kind of like this So the key

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thing is that if you have a you treat the electron, uh, just as a, as a single electron

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particle, you forget about the, the nuclear spin of the alkali metal. Uh, and you imagine

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there being a population here, which could be interconverted by a magnetic field. So this type

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of device, uh, as it's drawn here, involves a continuous pumping on the, the optical

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transition, uh, which transfers population over to this state here, but that it could be brought back

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again by the magnetic field. So if you're at exactly zero magnetic field, guess what? This will

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reach a saturation where all the population is here. And it leads to a maximum transmission of

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the light through the vapor. Whereas if you're at some magnetic field which is not zero, then this

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acts to reequilibrate these states. And then the vapor can always absorb more light. And you're

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more on this part of the curve. Um, okay. And then this is quite nice because it's it's very simple.

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It involves relatively few components. You just have your, your vapor and, um,

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light source photodetector and some coils. So an important thing to note is that this is

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an area of magnetic field sensing that's already gone through a MEMS revolution. We've gone through,

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uh, cells like this which have some flame seal. Uh, here, they're made on a kind

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of, uh, glassblowing manifold to something which can be made in bulk and this is

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a MEMS structure. So it has a silicone body. Um, this sorry is in

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centimeters. This ruler. Okay. Uh, how are these fabricated? They're done on a wafer scale, and it

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involves etching cavities in silicon. And then you plop on some some windows, and before you

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seal bond the whole thing shut, you will insert the alkali metal in a in an in an inert

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atmosphere. Uh, you bond all of that shut, and then you can cut this up with a dicing saw, and you can

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make many hundreds of these cells at a time. Uh, this there are there are various methods of

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introducing the alkali metal. I guess I'll just know that one of them involves, um, uh, is

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a little bit more friendly. That involves an azide salt of the alkali metal. So you have, uh,

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say rubidium azide or cesium azide, and you'll put a little droplet of that into, into

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the cavity and then you bond the the cell shut, and then you activate a

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thermal decomposition of the azide with UV light. And that generates the pure metal. And it also

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generates nitrogen gas which is a buffer buffer and quenching gas which is important for the

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these these reaching a high sensitivity. Um, okay.

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And this is uh, not not a new thing. So many, many groups and institutes have been developing these

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types of devices for different applications. I want to point out this one here. We worked with

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the Swiss um, Micro Fabrication Institute, uh, to develop this two

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chamber cell here. The reason why it has two chambers is that one is used for the azide

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filling. kind of a dirty backyard for for inserting rubidium into the cell. And then

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there's a clean chamber here, which is where we, uh, pass light through for magnetic field sensing, and

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there are some tiny micro channels that will connect these two. So even if there's, for example,

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incomplete decomposition of the azide, then it's matter. It's going to be left in in the backyard

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and it will not, for example, block up the windows. Okay. So this is all leading to something like

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lowering the cost, allowing us to integrate these into devices. Or maybe, maybe the fact that planar

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planar manufacturing is is more easily done by robots. Um, and that that helps the general effort

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of, uh, making things smaller. I want to highlight two innovations that that our group has made in

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this area. So one of them is to add extra functionality to these vapor cells. Um, here we

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had, uh, not just these type of cavity cells, um, with two windows, but we actually put

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platinum metal functionalization onto the windows. So you had heating wires, uh,

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Resistive heating wires and thermocouples that you could use to measure the temperature and

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control temperature gradients within the cell. So you could have a temperature gradient, which takes

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all of the rubidium access and condenses it in the backyard. So again the sensing chamber is

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clean, just like here for example. And this has been used

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in an atomic magnetometer. It reaches the kind of sensitivity that you would

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you would get with traditional glass blown vapor cells or without additional functionality. So

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there are some risks in doing this, this type of functionalization. What you don't want to do is

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add functionalization that also adds noise to the sensor because that's counter active okay.

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And another one concerns the coils. I mentioned that there is a zero field

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resonance phenomenon, which can be used to detect the magnetic fields. And that's one which is

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actually the most commonly used in the commercial magnetometers because it involves the fewest

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components. We developed a set of three, uh, three axis, um,

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PC, um, field coils that are just on two planes of a PCB. So you make a

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PCB printed circuit board, which has got, uh, traces on here, um, which will generate

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shim fields in, in X, Y, and z directions so that one can get this sensor,

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uh, operating at, at the zero field point, which is where it where it needs to be to detect the

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magnetic field. Uh, there are some constraints in this sort of design. Like you need to leave a hole

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for the light beam to pass through. Um, you also want to try and make this, um, set of

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coils as homogeneous as possible. Why? Because basically the T2 star of the the atom, the

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atomic spins is what determines the sensitivity or is what can limit the sensitivity. Um,

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so you could quantify that, for example through the linewidth of a free induction decay signal.

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And in this case there was a that design that was a design consideration where you want to minimize

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the, uh, inhomogeneity over the directions that matter. And you don't. And you can therefore

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afford to, uh, root traces, uh, over, over less homogeneous path for the direction that, that, uh, that

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doesn't really matter, which is along the beam. Okay. I want to say then

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that while these sensors are quite cool and they're very sensitive, um, they're not really

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optimized for, for NMR, um, they're optimized for a completely different application, which is, which

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is measuring the magnetic fields from, organs like the brain and the hearts, um,

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from outside the body So these are designed to be worn on the body as a, as a

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replacement technology for all type of squid sensors, which are used in, in MEG So in MEG

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you sit in this kind of while your head goes in the warm side of this cryostat. And then there's

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there are squid sensors. Um, the idea is to instead wear the sensors directly,

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which is possible because they're not cryogenic. Um, and then you can place them anywhere on the

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head that you like. Or people have different size heads, like kids and adults have very different

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size heads. Um, and this also accommodates moving the head rather than keeping your

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head fixed in a, in a in a certain position. So if you can imagine this type of,

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Um, brain imaging system in a hospital. Say, um, it gives you you can

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kind of roughly calculate how many sensors you might need to get started. Uh. Um, let's say you

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want 100 sensors, coverage over of the scalp, and then let's say you you're going for 100 of these

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imaging systems that's already, already going to be 10,000 vapor cells. And then, uh,

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you might need to have another factor of ten for yields. Um, so you're getting on for something like

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100,000 vapor cells. So then it's not only vapor cells, but it's individual

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magnetometer modules which are placed over the surface of the head. And there are a bunch of

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design considerations which I won't go into all of them, but many of them are similar to, um,

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what you might need if you were designing this type of magnetometer for NMR, like the fact that

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you're detecting a local field. So you want you want the atoms to be as close to the edge of the

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package as possible, rather than sitting somewhere in the middle. Um, and that's

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that's the same design criterion in The MEG because you want the sensor to be as close to the

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the surface of the skin as possible. Um, I'm going to get back to NMR in a

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second, but I want to say then that. So there are many, um, commercial prototypes of

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these sensors. You can buy them. They're quite highly optimized. Um, however, I think as you could

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probably see from the pictures here, that they don't look that, uh, able to be assembled by robots

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at the moment. Um, so we think that the innovations we've made could, if you design a magnetometer as

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a stack, which is completely robotically assembled, this would this would help in this area. Um,

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Also the the components that I showed you, uh, are also able to be

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made very, very cheaply. So the vapor cell and the field coils. Okay. Field coils is just a PCB. So

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that's extremely cheap. Uh, the vapor cells, you could imagine that being, um, I don't want to put a

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price label on it, but I think it would be about two orders of magnitude cheaper than per unit

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than you can currently get these vapor cells for if you make them at scale and therefore, uh, I

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don't think that, um, that buying these types of sensors and then trying to make an

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NMR instrument based off of this type of detection technology, um,

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is that smart of a move because, uh, basically this part of the sensor here in the middle is

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extremely cheap. Um, uh, it's like an insignificant cost compared to the rest of

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it. So the expensive part of these devices really is the laser at the moment. Um, the

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laser is about 90% of the cost of the device, so it's going to require certainly more than

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NMR, uh, to be interested. It's going to involve, I think, a lot more than MEG to be interested, to

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make these, these lasers on such a scale that, uh, that they become lower in

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price. These are certainly not made in the same type of volume as DVD lasers, which cost just a

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few euros each. So, um, we're talking orders of magnitude more than that. So I think that's a

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limitation. But if these types of magnetometers are going to be used in in small scale

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sensing, including NMR, then well that's a consideration. Okay. So I want to come

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back to NMR now. Uh, finally and um explore a little bit of a different direction, which is

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now less talking about the the sensor, but more about the type of system that we study with it.

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And so as we've kind of already heard, um, um, these types of

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sensors can be used in different ways. I usually like to show it like this, so that the already

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what's been done with alkali metal vapors and nuclear spins can be summarized with this picture.

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Uh, just the alkali metals by themselves as magnetometers or frequency standards.

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Um, many of you will know that you can use, uh, xenon or helium, uh, within the vapor

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cell to sense rotations and make gyroscopes. And also, if you have a way of

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introducing the the noble gas and taking it out of the cell without consuming the rubidium in the

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process, you can you can hyper polarize the gas and that's used in lung MRI and so on. And then

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the, the one which was mentioned in the previous talk, which is detecting the magnetic

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field from nuclear spins outside this box of atoms. So this is the this

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ZULF NMR detection technique. So it, it's limited by the ability to match the

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frequency of this system, uh, to the sensitive range of this system. So

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if you go to high in field, uh, the fact that these have different gyro magnetic ratios means

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that they're not going to crosstalk with one another. This was first done, um,

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around 2005. This example is from the Romalis lab. So they used a potassium

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magnetometer and they used, uh, water protons. And then again, thanks to the

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miniaturization which has been provided by, uh, MEG type wearable

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sensors, then this. This has got to the point where you can literally buy one of these. Get some

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sticky tape and you can sticky tape this to a solenoid, okay. Like this. And you can

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put some sample inside like water or, or some hetero nuclear system. And you can use that to

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detect either Larmor precision precession or some kind of J Coupling oscillation of the

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magnetization in the sample. I also want to mention that in this

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area there have been some other efforts. So there was a microfluidic, um, kind of

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flow cell. This is a remote detection, um NMR. It was also used for remote detection MRI with

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remote encoding. So you had a micro fabricated, um, cesium cell next to some channel

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and then a micro fabricated, noble gas polarizer. These were both

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at least ten years old. These works. And I think it's really a shame not to have seen more

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development in these areas. I think that they're really before their time. So if we were thinking

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about, um, low or low field NMR in a, in a chip scale

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setting, kind of along the lines that have been discussed from, from this network, I think that

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these ideas are well worth revisiting. Okay. What is the future? I want to talk about a few of the

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experiments that, um, that we've done in this area. So a few years ago we used, uh,

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magnetometers. So here's the rubidium vapor cell down here to measure fast field cycling, um,

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relaxation data sets. So from from proton. So if you have a sample which sits inside a

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polarizing coil which you can energize and then switch off and Then you can measure the

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relaxation rate as a function of the magnetic field, say between or nearly all the way down to

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DC and then up to say megahertz frequencies. And that was done on these

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kind of milliliter sized vials of liquid. So protons in water. And so we thought

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what would happen if we didn't use this type of sample. But we used something which was more

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interesting, more representative of a chip scale system. So this was a fiberglass 3D

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printed set of cavities. Um, we put that in the same instruments. Um,

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and the way to spatially resolve these cavities was simply to apply a field gradient

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along along the axis. So that resolved each of these little cavities into the peaks that you see

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here. Um, so it's it's still, say, very early, this set of experiments, but it's

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illustrating that small volumes are tolerable in in low magnetic

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field, uh, NMR with these types of sensors. Um, we could do something with contrast imaging or,

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uh, solvent relaxation, or we could add additional functionality like flow in these, in these types

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of devices, which you think is very interesting. Uh, we extended that to imaging. So

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in addition to the gradient along the field axis, then there was then a phase encoding along one of

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the other perpendicular axes. Um, so with these types of structures we could

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resolve water in the different cavities. Again it's not it's not sub micrometer scale magnetic

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resonance. Um, but it's magnetic resonance on samples which are very generous in terms of

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materials tolerance. And you could imagine putting all kinds of tubes or fittings, etc.

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etc. to make interesting devices. And we're also able to also able

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to show some kind of synergy here with the atomic sensors, because we moved the position of

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the sample with respect to the vapor cell. It's what these different images show. And so when the

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when the vapor cell is over a particular region of the sample, you're more sensitive to the NMR

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signal from that region. So here you see when the vapor cell is here then then there's you can kind

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of see the signal. And when it's down here and then you see this part of the sample, it's

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providing us some feedback on what the magnetometer is able to see. So we would be able

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to tune the size of the sample size of the vapor cell to the sample that's being looked at.

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Um, I don't think this in-situ prepolarization method is really the best one. It's, um,

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it's kind of slow. It involves lots of accumulations. So, uh, we, like many others, have been

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using shuttling system to move samples quickly between a high field prepolarization field and

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then the low field for detection. Um, back some time ago with Dimitri Sakellariou we

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made a permanent magnet, uh, which was just made of rectangular magnet blocks. And this reached a

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field of two Tesla. Um, for for this, uh, for, for this shuttling type of experiment that wasn't

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big enough. So we decided to increase the size of that magnet by a factor of two. Um, so these magnet

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blocks were no joke. They were one one inch by one inch by four inches. Um, but it was still it was

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still possible to put this array together by hand. And we think that we could, uh, maybe gain an extra

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factor of ten roughly in volume by by buying some bigger magnet blocks, another factor of two in

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size and making making some, uh, pre polarizing magnet.

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Okay. Um, I want to switch slightly again. Talk about high polarization

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hyperpolarization. Everything is better with hyperpolarization. Um, we use the fact that,

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uh, you can use a magnetometer to detect the DC magnetic moment of the sample. So without using

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any pulses. And the analogy here is just making a movie of magnetization, um,

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without with just looking at the spins and measuring, they're measuring their fields So if

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you have a vapor cell next to the sample and then there's some magnetization dynamics, then you

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could just look at that and the sensor will will see the signal. Um so we explored that

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with with para hydrogen. Um I think I won't go into detail on this in

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the interest of time, but there are some interesting magnetization dynamics that one can

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look at here and perhaps control or use feedback from hyperpolarization processes

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in real time. We also did this with SABRE. This is where

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instead of completely passively measuring the sample, we did something like toggling with pi

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pulses between plus and minus magnetization. Uh, and if you as long as you just

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toggle plus and minus plus and minus and back again, you can get a square wave signal. And then

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that lets you see the signal of some magnetization accumulation without without

25:02.279 --> 25:08.479
actually destroying it. And we did that also with dissolution DNP. So there are many examples there.

25:08.520 --> 25:13.078
We think that there are there are opportunities here for quality control of hyper polarized

25:13.079 --> 25:19.469
samples without without or instead of real time monitoring with these types of

25:19.469 --> 25:26.389
techniques. So there's clearly a lot of interesting applications of NMR at

25:26.389 --> 25:32.670
low field and. Applications and measurements with, with

25:32.670 --> 25:39.429
magnetometers. Um, it also should be in principle very simple. There are many,

25:39.430 --> 25:44.869
many, many motivations for that. You don't have many of the problems that you have in in high

25:44.910 --> 25:51.909
fields NMR spectroscopy. But a major block to that at the moment is the availability of

25:51.909 --> 25:58.749
instrumentation. So, uh, to put all of the operators together that you might

25:58.750 --> 26:05.510
need to build an ultra low field system, you might be kind of better of buying a high field

26:05.510 --> 26:11.749
system and doing some high field NMR with that, uh, maybe second hand. It kind of works out similar

26:11.749 --> 26:17.099
price. But as I mentioned then that the commercial op amps, we expect to see those come down in price,

26:17.420 --> 26:23.300
or expect to see those being significantly cheaper. If you don't buy something which is

26:23.300 --> 26:30.219
optimized for a different type of measurement. As for the console. So we developed that. We developed

26:30.219 --> 26:36.859
a console for uh sub megahertz NMR using Arduino. This is based

26:36.860 --> 26:42.619
on uh off the shelf component. So you can buy most of these from the electronics store. You can just

26:42.620 --> 26:48.060
put them together in the, in the, in the lab with soldering and everything fits on a credit card

26:48.099 --> 26:54.579
sized board. So you can just carry it around in your pocket. Okay. And we also shrunk the size of

26:54.579 --> 27:01.098
the magnetic shield. Um, the main cost of the magnetic shield is the, the material itself that

27:01.099 --> 27:07.139
it's made from. So if we, we half the size of the shield, uh, it becomes roughly a factor of ten

27:07.139 --> 27:13.059
cheaper. Uh, and then this one is about coffee mug size, so I like I really like the, the, the allusion

27:13.060 --> 27:20.049
to that in the, in the beginning of the meeting. Um, and then this is a simple enough system that we

27:20.050 --> 27:25.209
use it in teaching labs for, for students to learn about magnetic resonance and do pulse programing.

27:25.250 --> 27:32.089
So pulse programing is microsecond time resolution. Um, and you can also do simple

27:32.089 --> 27:36.609
experiments like you can program simple experiments like CPMG to measure a relaxation

27:36.609 --> 27:41.488
times and some, uh, hetero nuclear type experiments as well.

27:43.969 --> 27:50.769
Uh, okay. And we gave one of these to Ajoy's lab, and, um, this was around a couple of years ago when

27:50.769 --> 27:56.849
I went to EMC. I took one of these, and within one afternoon, we just completely replaced all of the

27:56.849 --> 28:02.930
electronics on, uh, ZULF type spectrometer that they were building. Um,

28:03.849 --> 28:09.889
got it all working. And a year later, then they produced some very nice results on multi-channel

28:09.889 --> 28:16.359
detection. Um, although still using these commercial sensors. But, uh, this is this is a very,

28:16.359 --> 28:23.079
very nice work. And, uh, um, they've come a long way with it. Okay. Uh, so

28:23.119 --> 28:30.080
I want, um, to kind of close this talk by, um, taking away

28:30.080 --> 28:36.919
that we can, we can use the fact that, um, these atomic, we leverage the fact that

28:36.920 --> 28:42.800
atomic vapor cells have been developed to a high technology because of other areas,like, like MEG.

28:42.840 --> 28:48.839
Um, and we could use those in NMR, but we could also use those in a, in any kind of other

28:48.839 --> 28:55.240
area of magnetic field sensing. Um, we also explored the possibility of just putting a vapor

28:55.240 --> 29:02.159
cell on a PCB. And so you can carry that around and put that in, put that in a physics experiment. Uh,

29:02.320 --> 29:09.279
this was a laser lock. So you simply have some hot vapor phase atoms here. It contains all

29:09.279 --> 29:16.269
of the heating type, uh, circuitary that you would need, uh, on the window of the vapor

29:16.269 --> 29:21.708
cell. it works just by finding the the absorption minimum of the vapor. And then you just

29:21.709 --> 29:28.509
lock to the you lock to that frequency. So it's as simple as inserting a lens into the beam, which is

29:28.510 --> 29:35.229
not not the case with things that you can buy these days. And then, um, I want to finish on one, um,

29:35.589 --> 29:41.948
unexpected thing that that came up in the course of these experiments, that ultra low field,

29:42.829 --> 29:49.669
uh, we so we discovered an interesting way of getting high resolution spectra. So, uh,

29:49.709 --> 29:56.510
you in very, very low magnetic fields where you have, uh, a crossover between strong coupling and

29:56.510 --> 30:02.389
weak coupling involving, uh, Zeeman Hamiltonian and J coupling Hamiltonian. You have what are called

30:02.389 --> 30:08.469
anti crossing fields. Um, so, uh, the molecule fumarate, for example, has got an anti crossing

30:08.499 --> 30:15.499
field and it happens around 400 nano Tesla. the definition of an anti crossing field is kind

30:15.499 --> 30:22.419
of where two states cross like that. And at the crossing point then you have this derivative

30:22.459 --> 30:29.338
of the frequency with respect to field is zero. So it means then that even if you have a small

30:29.339 --> 30:35.859
gradient then it's actually not going to broaden the line as much as it would for for T2 star. So

30:35.859 --> 30:42.818
for this molecule, it led to a very impressive, uh, decay constant. Um,

30:43.300 --> 30:47.219
and we're looking into that more. So there's certainly interesting things still to be explored

30:47.220 --> 30:53.539
in this ORF, even if we don't think about specifically about micro fabrication. Uh, now also

30:53.539 --> 30:59.379
interestingly, is that if we used a much more concentrated, uh, solution of fumarate, so we

30:59.620 --> 31:06.380
instead used a fully labeled version of the fumarate with carbon. This led to a much faster

31:06.380 --> 31:12.369
decay of that coherence. We think that's due to the fact that there are these distant dipolar

31:12.370 --> 31:18.529
field type effects which, which, which are big enough then that they actually do cause

31:18.530 --> 31:24.729
decoherence at the vapor. Okay. Anyway, that's something that's that's still being followed up.

31:24.930 --> 31:31.249
So I wonder then and I think we're in time. Um,

31:31.489 --> 31:38.448
by summarizing that, um, well, we kind of work in two

31:38.449 --> 31:44.369
areas. We work with magnetic with nuclear magnetic resonance, but we also work with magnetic sensors

31:44.929 --> 31:49.848
based on alkali vapors, which also destined for applications which have nothing to do with NMR.

31:49.890 --> 31:54.489
But there's a there's a lot of crosstalk and overlap in this area, and there's a lot of

31:54.490 --> 32:01.169
potential for miniaturize this and making, um, say, screening devices or relaxed symmetry

32:01.170 --> 32:07.839
devices at low field. Um, so we're still very much in the early stages of that. We don't

32:07.839 --> 32:14.679
study say systems, which are of, uh, super impressive chemical

32:14.680 --> 32:20.559
nature, but but it's going on. Um, and I also mentioned that there are there are going to be

32:20.560 --> 32:25.879
developments in the future that lead to these sensors becoming much more popular. The fact that

32:25.960 --> 32:31.159
MEMS technologies make these cheaper, and that there are other things in the pipeline as well,

32:31.200 --> 32:36.238
like there are some companies producing magnetometers which are not based on rubidium

32:36.239 --> 32:41.399
vapors, but based on other species like like helium. Okay. So then I just thank the people who

32:41.400 --> 32:47.239
founded the work, the collaborators and the rest of the team and yourselves. Thank you.

32:54.079 --> 32:59.519
Yeah. Thank you very much Michael for this very interesting and nice talk. Um, yes.

33:03.910 --> 33:10.469
Oh, thank you so much, Michael, for this fantastic talk. It's, uh, you always do magic with very cheap

33:10.470 --> 33:17.069
things. Very inspiring. Um, I have two quick, very quick, uh, comments and one

33:17.069 --> 33:23.509
question. Uh, the comments are that, um, your, um, uh, very narrow resonances near anti

33:23.510 --> 33:30.189
crossing. Uh, similar phenomena also happen in NV diamond. Uh, go by the name Morpheus or something

33:30.190 --> 33:37.109
like that, if I remember correctly. And they were studied, uh, for instance, uh, by many people, but

33:37.149 --> 33:44.149
uh, by Claudia Aviles at um in the Pines group some years ago. Um, and, um,

33:44.630 --> 33:51.429
the other comment is, uh, there is a large number of groups and companies in China that are

33:51.430 --> 33:57.948
into small magnetometers and, uh, in particular our former student Enam who

33:57.949 --> 34:04.859
started a company and they sell now, Um, uh, magnetometer that's very similar

34:04.860 --> 34:11.860
to Q spin, uh, in, uh, footprint. Uh, it is actually, uh, specifically optimized for

34:11.979 --> 34:18.019
ZULF NMR because its surface temperature is ten degrees lower and the cost is over another

34:18.020 --> 34:24.339
magnitude lower than the Q spin. So there's a lot happening. And it's by far not the

34:24.340 --> 34:30.939
only, um, company who does it. Okay. Those are my I will I just respond to that by saying,

34:30.939 --> 34:37.739
good., thanks for making me aware of those. I think that it's this, um, storyline that

34:37.740 --> 34:42.580
I've, that I've outlined here is, is a natural one. So I'm glad that other people are thinking of the

34:42.580 --> 34:49.379
same area and, and making progress in it. Yeah. And my quick question is you you showed that, uh, when

34:49.379 --> 34:54.739
you watch the movie of magnetization, which is cute, where, uh, there are some wiggles. Can you

34:54.740 --> 35:01.539
explain what the wiggles that you even modeled it, but you didn't explain where they come from? Uh,

35:01.739 --> 35:04.979
yeah. Shall I try and pull it up? I don't know how far back it was.

35:09.779 --> 35:16.459
Was it this one on this one? Um, okay. So it's

35:16.459 --> 35:23.379
perhaps easier to to understand the nature of the wiggles in the top. The top, uh, data set. Um,

35:23.379 --> 35:29.179
you can think of this like an adiabatic, uh, transition where you go from the north pole of

35:29.179 --> 35:34.459
the block sphere to the south pole of the block sphere. So a perfectly smooth adiabatic transition

35:34.460 --> 35:40.179
would be like following a meridian like that. But in reality, it's not like that. You always have

35:40.179 --> 35:45.700
some kind of precession about the field. So it it does this kind of trajectory. Uh, and those are

35:45.700 --> 35:52.659
called cycloid arcs. And so if you just take a projection of that, like onto, I guess onto the

35:52.659 --> 35:58.648
Z axis, then it looks like that curve I see. So it's not, it's not just um, uh, the

35:59.090 --> 36:03.889
hyperpolarization process, but the transfer of polarization that you're observing here. Right?

36:03.929 --> 36:10.809
Indeed. And then the the example at the bottom, why do you see much bigger wiggles? Uh, this is a

36:10.809 --> 36:17.809
system which is, uh, has lower magnetic equivalent symmetry of the hydrogens. So one

36:17.810 --> 36:24.009
way of saying that is the carbon makes the two protons look more magnetically and equivalent. Uh,

36:24.009 --> 36:30.810
and that leads to more polarization oscillation. A quick suggestion if you feed this

36:30.810 --> 36:37.129
back into the system, you can make a oscillator with this. And I will talk about it in my talk at

36:37.129 --> 36:43.889
the very end. Okay. Yeah. Yeah. Yeah.

36:43.930 --> 36:50.449
Great job. Thank you very much. I had an immediate question that came up was, uh,

36:50.570 --> 36:57.079
you make these vapor cells and, um, a very elegant process. How? How?

36:57.200 --> 37:03.280
What is the smallest size? You're allowed to make it so. In other words, you know,

37:04.439 --> 37:10.919
if I. If I told you I have a, you know, an Intel process with seven nanometers, we would be able to

37:10.959 --> 37:17.199
pattern something at seven nanometers. It would work, probably. But what would be the the what? The

37:17.199 --> 37:24.040
what? Yeah. What's the size limit? The how small these cells can. You can still make use of it. Yeah.

37:24.040 --> 37:30.560
There wasn't enough time to go into it. But a critical factor, um, in the sensitivity of these

37:30.560 --> 37:35.800
devices is then the relaxation time of the spins. And this, of course, depends if you think of gas

37:35.800 --> 37:42.799
phase at particles inside the cell, at some point when you make the cell

37:42.799 --> 37:49.319
smaller, you're going to run into wall collisions. So when the atoms collide with the walls then

37:49.319 --> 37:55.869
they will lose coherence. Um, you can do things like add certain coatings to the walls, which

37:55.870 --> 38:02.229
prevent relaxation. They provide elastic collisions, but there is a limit. And of course, as

38:02.229 --> 38:07.550
you shrink the size of the cell, you're also shrinking the the the number of atoms in the cell.

38:07.550 --> 38:14.428
So that's reducing the sensitivity. Yeah a follow up question on on on the cells, uh, how

38:14.429 --> 38:20.509
good the ceiling is of those cells. And do for example, do you notice, um, change of the, of the

38:20.510 --> 38:27.509
vapor volume over time. And how does that affect the performance? Um, that would

38:27.510 --> 38:33.869
help if I got a picture of one of the cells. So let's go back. Maybe to

38:33.909 --> 38:40.748
here. Something like that. Okay. This firstly, there's plenty of rubidium inside this cell.

38:41.310 --> 38:47.310
Um, the droplets here, uh, if you think if, if you operate at the cellar temperature,

38:47.990 --> 38:54.500
um, and you at some point, then the room, the the derivative rubidium leaves the cell

38:54.539 --> 39:01.299
by kind of permeating into the walls of the cell and of the glass. The glass firstly is

39:01.419 --> 39:08.059
covered with an alumina coating, which prevents permeation. Um, but additionally there's so much

39:08.060 --> 39:13.459
rubidium in the in the vapor cell that it would take a couple of years. I think it was ten years.

39:13.460 --> 39:19.659
We calculated for, for all of the rubidium to, to diffuse out. So there's so much rubidium in the

39:19.659 --> 39:26.419
cell because it needs a high nitrogen pressure for the, for the quenching, um, and for the buffer

39:26.419 --> 39:32.779
gas. Uh, and then because this is produced by azides. So rubidium is a bit like a

39:32.819 --> 39:39.378
byproduct. Um, you could, you could make these cells a slightly different way. So instead of you,

39:39.419 --> 39:46.419
instead of using so much azide, uh, which would create leftover rubidium. What you could do

39:46.419 --> 39:52.810
is do the bonding step under a higher back pressure. this is done in a commercial anodic

39:52.810 --> 39:57.489
bonding machine, which only goes up to a certain back pressure. I mean, you could put the whole

39:57.489 --> 40:02.929
thing in a pressurized room, but I think that would be that would be harder. Okay.

40:04.289 --> 40:05.649
Any further questions? Yeah.

40:11.330 --> 40:17.929
Yeah. Thanks, Michael. The quality requirements for the laser. You you

40:18.610 --> 40:25.249
went into that briefly that the laser is kind of a dominating element to the cost of the, uh, of the

40:25.249 --> 40:31.409
apparatus. So what are. Could you comment on what the quality requirements are for the laser

40:31.409 --> 40:35.849
radiation that's necessary for these measurements? Um.

40:38.209 --> 40:45.168
Okay, so these these are low power lasers, um, low power VCSEL lasers. And so

40:45.330 --> 40:50.679
low power, meaning around one milliwatts of infrared light. That's sufficient to get that

40:50.680 --> 40:57.159
level of ten femto Tesla sensitivity. Um, so these VCSEL can be produced

40:57.159 --> 41:03.359
in large batch quantities. So, you know, on a wafer scale, maybe you would have

41:03.360 --> 41:09.878
10,000 units on, on wafer, but there would of course be a yield

41:09.959 --> 41:15.519
factor. So there would be parts of the wafer which were lasing at the correct wavelength and some

41:15.520 --> 41:22.439
which were not lasing at the correct wavelength. The question or the issue really is scale. So if

41:22.439 --> 41:28.959
you had, um, if you went, if you went to one of the big laser manufacturers and said, I want to

41:28.960 --> 41:35.399
make a 7.95 nanometer laser for rubidium spectroscopy, um, with this

41:35.399 --> 41:42.158
recipe, they would say, great. Um, how many, how many millions of millions of units. So you can do

41:42.279 --> 41:48.709
to order. So for low production runs, it's not something which is very economical. And it's it's

41:48.709 --> 41:55.669
kind of difficult to do at the moment. Yes, yes. Yeah. I'm over

41:55.670 --> 42:00.269
here. So I have a very general question to the laser readout and the operational principle of

42:00.309 --> 42:04.709
the vapor cell. So the way I understood it, you shine a laser all the time, and then you look at

42:04.709 --> 42:10.628
the reduction in, in the, in the signal. So would you benefit from pulsing the lasers or you have

42:10.629 --> 42:16.549
it on initially. Then you let the system evolve in the dark. Yeah, exactly. This one. And then turn it

42:16.549 --> 42:23.269
on again. Or how much can you gain by this? Maybe this is actually the dynamic video you show. There

42:23.270 --> 42:29.229
are there are there are other types of schemes that one can use. So you could use, um, continuous

42:29.229 --> 42:36.029
pumping and slightly off resonance probing. Um, so but the cost of that is then you need two lasers

42:36.029 --> 42:42.149
at different frequencies. This is the one which is used. This method is the one which is used in all

42:42.149 --> 42:48.980
of these miniature MEG type magnetometers, because the fewest component is the simplest and

42:48.980 --> 42:55.978
smallest. The or easy to manufacture a small. So it's really just like this. And

42:55.979 --> 43:00.499
then you have to simply find a way of arranging those components small. It's not actually

43:00.500 --> 43:07.340
implemented like this. It's more implemented like an IQ modulation demodulation approach.

43:08.259 --> 43:15.139
So you're detecting the derivative around the peak here at zero field rather than uh, uh,

43:15.139 --> 43:20.139
rather than the absolute value of the transmission. Uh, but these are pretty robust

43:20.139 --> 43:25.099
things. So you can you can also make the electronics for this yourself out of Arduino. It's

43:25.100 --> 43:31.459
uh, that's not a factor of the cost of the devices. Is it a question I have. So with NV centers, uh,

43:31.500 --> 43:36.259
we can probe like you probe, but then we see the power broadening by the laser. So it's very

43:36.259 --> 43:42.299
beneficial to pump the laser, turn it off to the sensing, and turn the laser on again. So it's a

43:42.299 --> 43:49.129
similar type of letting the system evolve in the dark. Beneficial for wafer cells. Uh, it can

43:49.129 --> 43:56.129
be. So, um. Yeah. In this type of sensor, then if you increase the power level, there's a

43:56.129 --> 44:02.010
threshold where the power broadening reduces the sensitivity. It's that's not at the level that

44:02.010 --> 44:07.409
these laser VCSEL lasers can reach at the moment. But you could you could imagine an FID by

44:07.450 --> 44:14.209
magnetometer where you you pump the vapor to polarize it. And then you would

44:14.210 --> 44:19.529
turn off that pump and have a lower power probe. Yeah. So that's done quite often.

44:26.449 --> 44:33.329
Michael. Hello? Yeah. Michael. Thanks. Great talk. Um, I was wondering if you make these cells smaller,

44:33.370 --> 44:39.449
as you would if you use very many of them, then you should also need less laser power per cell.

44:39.929 --> 44:46.679
Right? Um. Or is that not right? Okay. So this is sort of

44:46.960 --> 44:53.079
related to the question that Jan asked. If you make the cell smaller, the cost is also that the

44:53.080 --> 44:59.879
number of sensing atoms decreases. So you want there is some kind of optimum if you want the if

44:59.879 --> 45:06.398
you want to maximize sensitivity, um, you would want to make your cell as big as, as

45:06.399 --> 45:13.279
tolerable. And also you would need to have a sufficient power of, uh, or you need to have a high

45:13.280 --> 45:19.199
enough temperature to use all of the available lights that you are shining on the vapor.

45:19.959 --> 45:26.719
Um, so it's a it's a multi parameter item. But but the reason to use many cells is to get a spatial

45:26.719 --> 45:32.759
resolution right from the, from the readout. Right. But these are separated by centimeter

45:32.760 --> 45:39.519
distances. Okay. But if you so if you go to millimeter distances could you then split the

45:39.520 --> 45:46.509
laser beam. Right. So that you use a few lasers to drive many such cells. It's possible. It it

45:46.509 --> 45:52.070
depends on the configuration. So you could have several vapor cells close together in a kind of

45:52.110 --> 45:58.070
little array. Um, that's not a good approach or that's not an approach for this zero field

45:58.070 --> 46:03.310
resonance, because you need to have a field modulation on each of the cells, and then you have

46:03.310 --> 46:10.309
crosstalk, and then it's going to become a mess. Yeah. But for if for cells which, uh, are far

46:10.310 --> 46:16.830
enough apart that there's no crosstalk,then, then that's an acceptable magnetometer strategy. But

46:16.830 --> 46:23.189
there are other, you know, like other types of strategy, like, uh, like FID. Thanks.

46:25.590 --> 46:32.549
Any further questions? Okay. If that's not

46:32.549 --> 46:35.469
the case, then let's thank Michael one more time. Thank you.

46:40.550 --> 46:40.790
Yeah.
