Four years ago, this paper caught my attention. The authors had made a structure with superconducting NbTiN contacts on top of a CrO2 film, with the intent of studying how superconductivity leaks into the chromium dioxide. The "leakage" of superconductivity into a non-superconducting metal is called the proximity effect. In a normal metal, the proximity effect extends over a spatial scale comparable to the coherence length, the distance that the electrons can travel before their quantum mechanical phases become scrambled due to inelastic processes (such as electron-electron scattering, or spin-flip scattering from magnetic impurities). The coherence length in a normal metal can be quite long at low temperatures - say a micron in a clean normal metal at 1 K.
Now, CrO2 is not a normal metal. Rather, it is a half-metal, an extreme limit of an itinerant ferromagnet, where all of the mobile charge carriers have the same spin polarization. This is important, because ordinary ("s-wave") superconducting correlations rely on pairing up electrons with opposite spins and momenta. If only one spin polarization is allowed, that should preclude any s-wave superconductivity. Practically speaking, in a typical ferromagnet with some magnetic exchange characterized by an exchange energy U, one can define an exchange length (in a diffusive material, given by sqrt(\hbar D/U), where D is the diffusion constant for the electrons) over which these correlations should die. For a strong ferromagnet, one finds that the exchange length is very short - a few nanometers or less. Knowing this, one would not expect to see any proximity induced superconductivity in a ferromagnet over longer distances. That's why this paper was surprising - the authors did see evidence of long-range (hundreds of nm) superconductivity in the ferromagnetic oxide. This implies some kind of unusual superconductivity in the ferromagnet - either p-wave pairing (when each pair of electrons in the superconducting material has one quantum of orbital angular momentum), or some more exotic state ("odd-frequency pairing", for the experts).
Several years passed, and no one reproduced this result. Until now. The authors of this new paper see the same sort of thing, and they try to explain in detail why this has been so hard to reproduce. The short version: CrO2 is a pain to work with.
Interestingly, there have been other signs of similar effects within the last year. For example, the Birge group at Michigan State has reported long-ranged proximity superconductivity induced in cobalt layers, though careful engineering of the contacts was required. Likewise, a Penn State collaboration has seen proximity superconductivity in Co nanowires hundreds of nm long. It's nice to see so much progress in this area lately.
A blog about condensed matter and nanoscale physics. Why should high energy and astro folks have all the fun?
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Tuesday, March 30, 2010
Monday, March 29, 2010
Slightly missing the point
I am, of course, pleased that Nature Materials ran a news item about our recent paper. However, they appear to have missed the point a bit. What we were trying to point out was that plotting data in scaled coordinates (current normalized by temperature to some power vs. voltage normalized by temperature, in this case) can be misleading. In this particular case, plotting temperature-independent data in this way on a log-log plot can make it look like the data all collapse onto some universal curve (with deep implications). In fact, the data themselves aren't doing any such thing - the apparent collapse is due to a flawed plotting procedure. Ross McKenzie got this point immediately. Ahh well. Bottom line: be very careful when plotting "scaled" quantities, to make sure that you're not biasing yourself toward a particular conclusion.
Wednesday, March 24, 2010
Three years of hindsight
Back in February, 2007, I mentioned that I thought that making and measuring nanostructures directly out of strongly correlated materials was a promising research direction. I still think so, in part because of the experiences my lab and others have had in the mean time. As I've mentioned before, strongly correlated materials are those where we can no longer get away with our (often miraculously good) simple single-particle description of electronic structure that ignores the electron-electron interaction. Examples of correlated materials include the high temperature superconductors and various transition metal oxides. In the high Tc case, single-particle band structure says that the undoped parent compound should be a metal, when it's found instead to be an antiferromagnetic insulator. Strongly correlated materials often display a rich variety of interesting electronic states as well as phase transitions between them.
Why nanostructures? Three main reasons. First, when some strongly correlated materials go through electronic (and structural, sometimes) transitions, they display inhomogeneities. For example, when vanadium dioxide goes through its metal-insulator transition (from below) near 341 K, metallic domains nucleate and grow, eventually encompassing the whole material. Nanostructures can allow you to access such materials on the scale of individual domains, as was done here and here in VO2, and here in a colossal magnetoresistance oxide.
Second, nanospaced electrodes allow you to use electric field as an interesting perturbation, and to tell the difference between effects driven by voltage (or energy) and those actually driven by field. For example, in this paper (very influential and highly cited), the authors found that a charge-ordered oxide could be kicked out of an insulating state and into a low resistance state when around 1000 V was applied across a 1mm crystal of the material. That's cool, and prompted much work, but as an experimentalist one always wonders whether the 106 V/m electric field is responsible (which would be particularly interesting), or whether the energy available to the electrons is actually doing some kind of chemistry or damage to the material. In a nanostructured system, one could get the same electric field by applying 100 mV across electrodes separated by 100 nm, getting big fields without big available energies. We've done work along these lines in Fe3O4, and have had quite a bit of fun with it.
Third, nanospaced electrodes are a way of driving systems far from equilibrium and potentially measuring them under those conditions. When an ordinary electron is injected into a correlated material, it can be thought of as a superposition of the "natural" low-energy excitations of the correlated system. For example, in a Luttinger liquid, the injected carrier "fractionalizes" into a spinon (spin-1, chargeless mode) and a holon (charged, spinless mode). Truly nano-spaced measurements may be a means of catching this process in action, though it won't be easy!
I still think that this is a fun and exciting area, and interest appears to be growing.
Why nanostructures? Three main reasons. First, when some strongly correlated materials go through electronic (and structural, sometimes) transitions, they display inhomogeneities. For example, when vanadium dioxide goes through its metal-insulator transition (from below) near 341 K, metallic domains nucleate and grow, eventually encompassing the whole material. Nanostructures can allow you to access such materials on the scale of individual domains, as was done here and here in VO2, and here in a colossal magnetoresistance oxide.
Second, nanospaced electrodes allow you to use electric field as an interesting perturbation, and to tell the difference between effects driven by voltage (or energy) and those actually driven by field. For example, in this paper (very influential and highly cited), the authors found that a charge-ordered oxide could be kicked out of an insulating state and into a low resistance state when around 1000 V was applied across a 1mm crystal of the material. That's cool, and prompted much work, but as an experimentalist one always wonders whether the 106 V/m electric field is responsible (which would be particularly interesting), or whether the energy available to the electrons is actually doing some kind of chemistry or damage to the material. In a nanostructured system, one could get the same electric field by applying 100 mV across electrodes separated by 100 nm, getting big fields without big available energies. We've done work along these lines in Fe3O4, and have had quite a bit of fun with it.
Third, nanospaced electrodes are a way of driving systems far from equilibrium and potentially measuring them under those conditions. When an ordinary electron is injected into a correlated material, it can be thought of as a superposition of the "natural" low-energy excitations of the correlated system. For example, in a Luttinger liquid, the injected carrier "fractionalizes" into a spinon (spin-1, chargeless mode) and a holon (charged, spinless mode). Truly nano-spaced measurements may be a means of catching this process in action, though it won't be easy!
I still think that this is a fun and exciting area, and interest appears to be growing.
Sunday, March 21, 2010
March Meeting wrap-up
The March Meeting is over, and overall it was good, as usual, and far too large, as usual. Clearly the favorite topics this year were topological insulators, graphene, and iron pnictide superconductors. On Thursday I did see a very good invited session on scanned probe microscopy, including examinations of vortices in the iron pnictides (among other things) and careful measurements of spin excitations at the atomic scale (that last being a substitute talk by Prof. Hla of Ohio University). I had good discussions with colleagues from other places, got some good ideas for different experimental techniques, and looked at all the gadgets being hawked by vendors. Clearly the era of the cryogen-free dilution refrigerator is upon us, if you can actually get any 3He, have a spare couple of hundred thousand dollars, and can support a 6-10 kW compressor. I was disappointed by turnout at an invited session that I'd helped organize (more in a separate post), but it was up against a session with talks by three Nobel laureates. On the return flight, I had a fun time talking with the neighboring passenger, the drummer for Ra Ra Riot, on his way to a gig in Austin. Good to be home, though.
Thursday, March 18, 2010
Physics for Everyone
This was the title of an invited session yesterday at the APS meeting. Ivan Schuller put together a very interesting collection of talks, with subjects of broad interest to a large audience. Ray Orbach gave an updated version of his presentation about the global energy challenge, including a strong plea that the US re-start reprocessing spent nuclear fuel (an idea I've held for a long time, so clearly it has merit :-) ). Ted Postol spoke about his ideas on ballistic missile defense. Charles Falco presented his recent work on converting digital cameras from conventional visible light photography to infrared (and recently ultraviolet) wavelengths, and using those cameras to look at art works. Fascinating stuff. Eugenie Reich gave a half-hour talk to a packed room about Hendrik Schön (see this pdf for the whole megillah), based on her book. No revelations, and surprisingly little discussion of co-author/collaborator responsibilities. She did have some amusing graphs, like the one displaying Schön's publications vs. time next to the Lucent stock price vs. time. Finally, the session closed with a fun talk by Alan Nathan about the physics of baseball. These kinds of sessions are a great feature of large meetings, though they must be a lot of work to put together.
Wednesday, March 17, 2010
March Meeting - minor update
I'm at the APS March Meeting, and as it is every year, it's really too big. I've largely been spending much of my time at sessions where my students are speaking or where I'm chairing. One major point of the meeting is the networking that takes place away from the talks. Even in these days of modern communications technology, there is still no substitute for sitting down at a table with someone and hashing out a problem with a pen and a pad of paper.
There are two types of talks: invited talks (30 min + 6 min for questions) and contributed talks (10 min + 2 min for questions). Contributed talks are usually most useful to specialists in a field, since with that kind of time constraint it's almost impossible to give an intro to something new. Occasionally, however, it is possible to learn something new from a contributed talk. I just saw an excellent one by Kieron Burke of UC Irvine, speaking about how one can get from density functional theory (which sometimes feels like a mysterious black art) and get back to simple Thomas-Fermi theory. The relevant paper is here, and I really do feel like I learned something. More later....
There are two types of talks: invited talks (30 min + 6 min for questions) and contributed talks (10 min + 2 min for questions). Contributed talks are usually most useful to specialists in a field, since with that kind of time constraint it's almost impossible to give an intro to something new. Occasionally, however, it is possible to learn something new from a contributed talk. I just saw an excellent one by Kieron Burke of UC Irvine, speaking about how one can get from density functional theory (which sometimes feels like a mysterious black art) and get back to simple Thomas-Fermi theory. The relevant paper is here, and I really do feel like I learned something. More later....
Monday, March 15, 2010
Peer review idiocy
In the Wall Street Journal over this past weekend, Peter Berkowitz argues that peer review is a corrupt system with no objectivity and little value. He says this in connection with the climate science kerfluffle, claiming that peer review makes it easy for scholars to reward friends and punish enemies. He argues by analogy: we don't let athletes referee their own games, so why should we allow scholars to do the equivalent? He does somehow seem aware that there is a real fundamental problem with ditching the system, though - the ability to competently evaluate intellectual work requires actual expertise. I think Berkowitz gravely underestimates the qualification/expertise problem when it comes to actual physical science. Sometimes the particular technical areas are incredibly challenging, requiring years of study to appreciate the subtle problems and issues. Your choice is to let the people who have done such legwork do your evaluations, or to let people without the proper background make decisions. Those of us who do science know that peer review has its set of problems, but, like democracy, it's the worst system except for all the alternatives. Harping on its flaws without having a real discussion of these difficulties or offering alternatives is just intellectually lazy.
Saturday, March 13, 2010
Narrowcasting.
I know that this will appeal to a differentially small fraction of my readership, but as a native of Pittsburgh of a certain age I am compelled to share this video. An actual science post will follow tomorrow. (For those readers that have never spoken with me, no, I do not talk with this kind of accent. But I can.)
Monday, March 08, 2010
Self-promotion, travel, and talking heads
I'm going to be doing some travel this week, and next week is the APS March Meeting in Portland, OR, so blog posts are likely to be thin. I will try to write a bit about the APS.
In the meantime, I wanted to point out our new paper about shot noise measurements in atomic-scale junctions. This is the paper I was talking about when posting about (good!) referees. The referee reports were very helpful in making our presentation much more clear here.
Lastly, with my previous post about being a nanoscale science "talking head", I wanted to point out this terrific video that shows many of the things wrong with TV journalism today. The dry British sense of humor is tough to beat.
In the meantime, I wanted to point out our new paper about shot noise measurements in atomic-scale junctions. This is the paper I was talking about when posting about (good!) referees. The referee reports were very helpful in making our presentation much more clear here.
Lastly, with my previous post about being a nanoscale science "talking head", I wanted to point out this terrific video that shows many of the things wrong with TV journalism today. The dry British sense of humor is tough to beat.
Wednesday, March 03, 2010
Comedy Central: better science than the Science Channel?
Zapperz wrote an interesting post that links to an article in USA Today about whether Comedy Central (specifically The Daily Show and The Colbert Report) give some of the best real science coverage on television. They bring on actual scientists (Neil Degrasse Tyson, Sean Carroll, Brian Greene, Lisa Randall, Steven Chu, Bob Park (!)) and have conversations with them that last more than a 30 second sound bite. I notice that there are no nano folks on the guest lists for either show over the last couple of years. Clearly this is a clarion call to write a general audience book and try to go on there to promote it; either that, or to try and be their go-to person to debunk outrageous claims about nanotechnological dystopias.
Monday, March 01, 2010
Topological insulators
A very big story in recent years in condensed matter physics is that of topological insulators, and it's a great tale of finding something new "in plain sight". For something like 70 or 80 years, physicists thought that they had a handle on the insulating state. Take a large crystalline solid, and ignore electron-electron interactions for the moment. The allowed electronic states for such a material come in bands, when you look at how they're distributed as a function of energy. That is, there are many electronic states clustered so close together in energy, separated by energy gaps where there are no allowed electronic states. Now consider filling up those states with some number of electrons, counting two electrons (one spin up, one spin down) per state. (This is short-hand for something more sophisticated, but it gets the point across, just as filling up atomic orbitals does a pretty good job describing the periodic table.) If you end up in the middle of a band, with lots of empty states right next to the filled states in energy, then you have a metal. If you end up exactly filling a band, then you have either a band insulator (if the energy gap next to the most energetic filled state is several eV) or a semiconductor (if the energy gap is more like 1-3 eV). Turning on electron-electron interactions can change things a bit, but not too much. (Interactions can lead to one more kind of insulator, a Mott insulator, in which interactions open up a gap in what would otherwise have been a metallic system.)
Until recently, we thought that this was all there was to it, as far as band insulators go. It turns out that this is not the case, because of what happens at the boundary of the material (which we have so far been ignoring). In some band insulators, the surface states (in 3d) or edge states (in 2d) can have special properties. For example, one could have a situation where (because of spin-orbit coupling + band structure) the right-moving charge carriers have to have their spin pointed in one direction, while the left-moving charge carriers have to have their spin pointed the opposite way. The result is that these surface states with unusual Dirac-like dispersion are thought to be able to resist back-scattering very effectively. This means that these surface states may be very interesting for electronics applications, having ballistic properties over long distances. Moreover, these properties are expected to be rather robust, because they come from the topology of the states, which is not easily disturbed by disorder. For great reviews of this, see this paper (soon to appear in RMP), this article in Physics Today, and this video.
There is evidence that these states do exist, particularly from surface scattering techniques such as ARPES. Transport experiments have faced a challenge, however, since many of the candidate materials (Bi2Se3, for example) are difficult to grow in sufficient purity that the bulk is actually insulating. Still, this is exciting stuff, and a new paper on the arxiv (1003.0155) reveals that there may be a whole new class of other materials to play with. Surprises from nature are always fun.
Until recently, we thought that this was all there was to it, as far as band insulators go. It turns out that this is not the case, because of what happens at the boundary of the material (which we have so far been ignoring). In some band insulators, the surface states (in 3d) or edge states (in 2d) can have special properties. For example, one could have a situation where (because of spin-orbit coupling + band structure) the right-moving charge carriers have to have their spin pointed in one direction, while the left-moving charge carriers have to have their spin pointed the opposite way. The result is that these surface states with unusual Dirac-like dispersion are thought to be able to resist back-scattering very effectively. This means that these surface states may be very interesting for electronics applications, having ballistic properties over long distances. Moreover, these properties are expected to be rather robust, because they come from the topology of the states, which is not easily disturbed by disorder. For great reviews of this, see this paper (soon to appear in RMP), this article in Physics Today, and this video.
There is evidence that these states do exist, particularly from surface scattering techniques such as ARPES. Transport experiments have faced a challenge, however, since many of the candidate materials (Bi2Se3, for example) are difficult to grow in sufficient purity that the bulk is actually insulating. Still, this is exciting stuff, and a new paper on the arxiv (1003.0155) reveals that there may be a whole new class of other materials to play with. Surprises from nature are always fun.
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