Tag Archives: imaging

TRIUMF accelerator used by US researchers to visualize properties of nanoscale materials

The US researchers are at the University of California at Los Angeles (UCLA) and while it’s not explicitly stated I’m assuming the accelerator they mention at TRIUMF (Canada’s national laboratory for particle and nuclear physics) has something special as there are accelerators in California and other parts of the US.

A July 15, 2015 news item on Nanotechnology Now announces the latest on visualizing the properties of nanoscale materials,

Scientists trying to improve the semiconductors that power our electronic devices have focused on a technology called spintronics as one especially promising area of research. Unlike conventional devices that use electrons’ charge to create power, spintronic devices use electrons’ spin. The technology is already used in computer hard drives and many other applications — and scientists believe it could eventually be used for quantum computers, a new generation of machines that use quantum mechanics to solve complex problems with extraordinary speed.

A July 15, 2015 UCLA news release, which originated the news item, expands on the theme and briefly mentions TRIUMF’s accelerator (Note: A link has been removed),

Emerging research has shown that one key to greatly improving performance in spintronics could be a class of materials called topological insulators. Unlike ordinary materials that are either insulators or conductors, topological insulators function as both simultaneously — on the inside, they are insulators but on their exteriors, they conduct electricity.

But topological insulators have certain defects that have so far limited their use in practical applications, and because they are so tiny, scientists have so far been unable to fully understand how the defects impact their functionality.

The UCLA researchers have overcome that challenge with a new method to visualize topological insulators at the nanoscale. An article highlighting the research, which was which led by Louis Bouchard, assistant professor of chemistry and biochemistry, and Dimitrios Koumoulis, a UCLA postdoctoral scholar, was published online in the Proceedings of the National Academy of Sciences.

The new method is the first use of beta‑detected nuclear magnetic resonance to study the effects of these defects on the properties of topological insulators.

The technique involves aiming a highly focused stream of ions at the topological insulator. To generate that beam of ions, the researchers used a large particle accelerator called a cyclotron, which accelerates protons through a spiral path inside the machine and forces them to collide with a target made of the chemical element tantalum. This collision produces lithium-8 atoms, which are ionized and slowed down to a desired energy level before they are implanted in the topological insulators.

In beta‑detected nuclear magnetic resonance, ions (in this case, the ionized lithium-8 atoms) of various energies are implanted in the material of interest (the topological insulator) to generate signals from the material’s layers of interest.

Bouchard said the method is particularly well suited for probing regions near the surfaces and interfaces of different materials.

In the UCLA research, the high sensitivity of the beta‑detected nuclear magnetic resonance technique and its ability to probe materials allowed the scientists to “see” the impacts of the defects in the topological insulators by viewing the electronic and magnetic properties beneath the surface of the material.

The researchers used the large TRIUMF cyclotron in Vancouver, British Columbia.

According to the UCLA news release, there were also researchers from the University of British Columbia, the University of Texas at Austin and Northwestern University *were* involved with the work.

Here’s a link to and a citation for the paper,

Nanoscale β-nuclear magnetic resonance depth imaging of topological insulators by Dimitrios Koumoulis, Gerald D. Morris, Liang He, Xufeng Kou, Danny King, Dong Wang, Masrur D. Hossain, Kang L. Wang, Gregory A. Fiete, Mercouri G. Kanatzidis, and Louis-S. Bouchard. PNAS July 14, 2015 vol. 112 no. 28 doi: 10.1073/pnas.1502330112

This paper is behind a paywall.

*’were’ added Jan. 20, 2016.

Making carbon nanoparticles at home with honey or molasses

No need to rush and buy any ingredients as the University of Illinois at Urbana-Champaign researchers do not provide a recipe for cooking up carbon nanoparticles. However, it is diverting to think that one day we might be able to make these items at home. From a June 19, 2015 news item by Stuart Milne on the Azonano website,

Researchers at the University of Illinois have discovered an easy method to produce carbon nanoparticles for biomedical applications. These carbon nanoparticles can be made at home within a couple of hours using easily available ingredients and molasses.

A June 19 (?), 2015 University of Illinois at Urbana-Champaign news release (also on EurekAlert) provides more detail about the research,

“If you have a microwave and honey or molasses, you can pretty much make these particles at home,” Pan [professor Dipanjan Pan] said. “You just mix them together and cook it for a few minutes, and you get something that looks like char, but that is nanoparticles with high luminescence. This is one of the simplest systems that we can think of. It is safe and highly scalable for eventual clinical use.”

These “next-generation” carbon spheres have several attractive properties, the researchers found. They naturally scatter light in a manner that makes them easy to differentiate from human tissues, eliminating the need for added dyes or fluorescing molecules to help detect them in the body.

The nanoparticles are coated with polymers that fine-tune their optical properties and their rate of degradation in the body. The polymers can be loaded with drugs that are gradually released.

The nanoparticles also can be made quite small, less than eight nanometers in diameter (a human hair is 80,000 to 100,000 nanometers thick).

“Our immune system fails to recognize anything under 10 nanometers,” Pan said. “So, these tiny particles are kind of camouflaged, I would say; they are hiding from the human immune system.”

The team tested the therapeutic potential of the nanoparticles by loading them with an anti-melanoma drug and mixing them in a topical solution that was applied to pig skin.

Bhargava’s [professor Rohit Bhargava] laboratory used vibrational spectroscopic techniques to identify the molecular structure of the nanoparticles and their cargo.

“Raman and infrared spectroscopy are the two tools that one uses to see molecular structure,” Bhargava said. “We think we coated this particle with a specific polymer and with specific drug-loading – but did we really? We use spectroscopy to confirm the formulation as well as visualize the delivery of the particles and drug molecules.”

The team found that the nanoparticles did not release the drug payload at room temperature, but at body temperature began to release the anti-cancer drug. The researchers also determined which topical applications penetrated the skin to a desired depth.

In further experiments, the researchers found they could alter the infusion of the particles into melanoma cells by adjusting the polymer coatings. Imaging confirmed that the infused cells began to swell, a sign of impending cell death.

“This is a versatile platform to carry a multitude of drugs – for melanoma, for other kinds of cancers and for other diseases,” Bhargava said. “You can coat it with different polymers to give it a different optical response. You can load it with two drugs, or three, or four, so you can do multidrug therapy with the same particles.”

“By using defined surface chemistry, we can change the properties of these particles,” Pan said. “We can make them glow at a certain wavelength and also we can tune them to release the drugs in the presence of the cellular environment. That is, I think, the beauty of the work.”

Here’s a link to and a citation for the paper,

Tunable Luminescent Carbon Nanospheres with Well-Defined Nanoscale Chemistry for Synchronized Imaging and Therapy by Prabuddha Mukherjee, Santosh K. Misra, Mark C. Gryka, Huei-Huei Chang, Saumya Tiwari, William L. Wilson, John W. Scott, Rohit Bhargava, and Dipanjan Pan. Small
DOI: 10.1002/smll.201500728 Article first published online: 20 MAY 2015

© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

This paper is behind a paywall.

Nanoscale imaging gets rough

Smooth is easier than rough when imaging at the nanoscale according to a June 17, 2015 Northwestern University news release by Megan Fellman (also on EurekAlert),

A multi-institutional team of scientists has taken an important step in understanding where atoms are located on the surfaces of rough materials, information that could be very useful in diverse commercial applications, such as developing green energy and understanding how materials rust.

Researchers from Northwestern University, Brookhaven National Laboratory, Lawrence Berkeley National Laboratory and the University of Melbourne, Australia, have developed a new imaging technique that uses atomic resolution secondary electron images in a quantitative way to determine the arrangement of atoms on the surface.

Many important processes take place at surfaces, ranging from the catalysis used to generate energy-dense fuels from sunlight and carbon dioxide to how bridges and airplanes corrode, or rust. Every material interacts with the world through its surface, which is often different in both structure and chemistry from the bulk of the material.

The real focus of the work is on corrosion, according to the news release,

“We are excited by the possibilities of applying our imaging technique to corrosion and catalysis problems,” said Laurence Marks, a co-author of the paper and a professor of materials science and engineering at Northwestern’s McCormick School of Engineering and Applied Science. “The cost of corrosion to industry and the military is enormous, and we do not understand everything that is taking place. We must learn more, so we can produce materials that will last longer.”

To understand these processes and improve material performance, it is vital to know how the atoms are arranged on surfaces. While there are many good methods for obtaining this information for rather flat surfaces, most currently available tools are limited in what they can reveal when the surfaces are rough.

Scanning electron microscopes are widely used to produce images of many different materials, and roughness of the surface is not that important. Until very recently, instruments could not obtain clear atomic images of surfaces until a group at Brookhaven managed in 2011 to get the first images that seemed to show the surfaces very clearly. However, it was not clear to what extent they really were able to image the surface, as there was no theory for the imaging and many uncertainties.

The new work has answered all these questions, Marks said, providing a definitive way of understanding the surfaces in detail. What was needed was to use a carefully controlled sample of strontium titanate and perform a large range of different types of imaging to unravel the precise details of how secondary electron images are produced.

“We started this work by investigating a well-studied material,” said Jim Ciston, a staff scientist at Lawrence Berkeley National Laboratory and the lead author of the paper, who obtained the experimental images. “This new technique is so powerful that we had to revise much of what was already thought to be well-known. This is an exciting prospect because the surface of every material can act as its own nanomaterial coating, which can greatly change the chemistry and behavior.”

“The beauty of the technique is that we can image surface atoms and bulk atoms simultaneously,” said Yimei Zhu, a scientist at Brookhaven National Laboratory. “Currently, no existing methods can achieve that.”

Les Allen, who led the theoretical and modeling aspects of the new imaging technique in Melbourne, said, “We now have a sophisticated understanding of what the images mean. It now will be full steam ahead to apply them to many different types of problems.”

Here’s a link to and citation for the paper,

Surface determination through atomically resolved secondary-electron imaging by J. Ciston, H. G. Brown, A. J. D’Alfonso, P. Koirala, C. Ophus, Y. Lin, Y. Suzuki, H. Inada, Y. Zhu, L. J. Allen, & L. D. Marks. Nature Communications 6, Article number: 7358 doi:10.1038/ncomms8358 Published 17 June 2015

This paper is open access.

Microbubbles reform into nanoparticles after bursting

It seems researchers at the Toronto-based (Canada), Princess Margaret Cancer Centre, have developed a new theranostic tool made of microbubbles used for imaging that are then burst into nanoparticles delivering therapeutics. From a March 30, 2015 news item on phys.org,

Biomedical researchers led by Dr. Gang Zheng at Princess Margaret Cancer Centre have successfully converted microbubble technology already used in diagnostic imaging into nanoparticles that stay trapped in tumours to potentially deliver targeted, therapeutic payloads.

The discovery, published online today [March 30, 2015] in Nature Nanotechnology, details how Dr. Zheng and his research team created a new type of microbubble using a compound called porphyrin – a naturally occurring pigment in nature that harvests light.

A March 30, 2015 University Health Network news release on EurekAlert, which originated the news item, describes the laboratory research on mice,

In the lab in pre-clinical experiments, the team used low-frequency ultrasound to burst the porphyrin containing bubbles and observed that they fragmented into nanoparticles. Most importantly, the nanoparticles stayed within the tumour and could be tracked using imaging.

“Our work provides the first evidence that the microbubble reforms into nanoparticles after bursting and that it also retains its intrinsic imaging properties. We have identified a new mechanism for the delivery of nanoparticles to tumours, potentially overcoming one of the biggest translational challenges of cancer nanotechnology. In addition, we have demonstrated that imaging can be used to validate and track the delivery mechanism,” says Dr. Zheng, Senior Scientist at the Princess Margaret and also Professor of Medical Biophysics at the University of Toronto.

Conventional microbubbles, on the other hand, lose all intrinsic imaging and therapeutic properties once they burst, he says, in a blink-of-an-eye process that takes only a minute or so after bubbles are infused into the bloodstream.

“So for clinicians, harnessing microbubble to nanoparticle conversion may be a powerful new tool that enhances drug delivery to tumours, prolongs tumour visualization and enables them to treat cancerous tumours with greater precision.”

For the past decade, Dr. Zheng’s research focus has been on finding novel ways to use heat, light and sound to advance multi-modality imaging and create unique, organic nanoparticle delivery platforms capable of transporting cancer therapeutics directly to tumours.

Interesting development, although I suspect there are many challenges yet to be met such as ensuring the microbubbles consistently arrive at their intended destination in sufficient mass to be effective both for imaging purposes and, later, as nanoparticles for drug delivery purposes.

Here’s a link to and citation for the paper,

In situ conversion of porphyrin microbubbles to nanoparticles for multimodality imaging by Elizabeth Huynh, Ben Y. C. Leung, Brandon L. Helfield, Mojdeh Shakiba, Julie-Anne Gandier, Cheng S. Jin, Emma R. Master, Brian C. Wilson, David E. Goertz, & Gang Zheng. Nature Nanotechnology (2015) doi:10.1038/nnano.2015.25 Published online 30 March 2015

This paper is behind a paywall but a free preview is available via ReadCube Access.

This is one of those times where I’m including the funding agencies and the ‘About’ portions of the news release,

The research published today was funded by the Canadian Institutes of Health Research (CIHR) Frederick Banting and Charles Best Canada Graduate Scholarship, the Emerging Team Grant on Regenerative Medicine and Nanomedicine co-funded by the CIHR and the Canadian Space Agency, the Natural Sciences and Engineering Research Council of Canada, the Ontario Institute for Cancer Research, the International Collaborative R&D Project of the Ministry of Knowledge Economy, South Korea, the Joey and Toby Tanenbaum/Brazilian Ball Chair in Prostate Cancer Research, the Canada Foundation for Innovation and The Princess Margaret Cancer Foundation.

About Princess Margaret Cancer Centre, University Health Network

The Princess Margaret Cancer Centre has achieved an international reputation as a global leader in the fight against cancer and delivering personalized cancer medicine. The Princess Margaret, one of the top five international cancer research centres, is a member of the University Health Network, which also includes Toronto General Hospital, Toronto Western Hospital and Toronto Rehabilitation Institute. All are research hospitals affiliated with the University of Toronto. For more information, go to http://www.theprincessmargaret.ca or http://www.uhn.ca .

I was not expecting to see South Korea or Brazil mentioned in the funding. Generally, when multiple countries are funding research, their own research institutions are also involved. As for the Princess Margaret Cancer Centre being one of the top five such centres internationally, I wonder how these rankings are determined.

Stefan Eisebitt and his team at Helmholtz-Zentrum Berlin (HZB) reduce the jitters with new holographic method

A Jan. 7, 2014 news item on Nanowerk highlights a new technique for achieving high resolution imaging of dynamic processes at the nanoscale,

The efficiency of the new method is based on a X-ray focussing optics being firmly fixed to the object to be imaged. While this approach initially provides a blurry image, this can be focussed in the computer based on the hologram information. At the same time, the rigid connection between the object and the focussing optics elegantly solves the problem of vibration induced jitter that plays an enormous role at the nanometre scale.

Prof. Stefan Eisebitt, who heads the division Nanometre and X-Ray Optics at Technische Universität Berlin  and  the joint research group Functional Nanostructures at Helmholtz-Zentrum Berlin (HZB), explains: “Just as a fast objective lens on a camera enables you to get a sharp image even under conditions of weak lighting, our optical element here enables the X-ray light to be used more efficiently as well. At the same time, we have firmly coupled this X-ray lens with the object to be imaged so that vibrations no longer have any detrimental influence and the image is stabilised.” As a consequence, low-contrast or moving nanoobjects can be imaged notably better.

The Jan. 7, 2014 Helmholtz-Zentrum Berlin (HZB) press release (also on EurekAlert), which originated the news item, provides more specific details about the problem and about the new method,

For X-ray holography, you need coherent light – light whose electromagnetic waves oscillate synchronously. This is the kind of light produced by lasers or by synchrotron sources like BESSY II. In the holographic process used here, part of the X-ray light falls on the object and part of it carries on through a pinhole aperture placed laterally beside the object to create the reference wave. A hologram is formed by superposing the two waves and recording the result with a detector. A holographic image of the illuminated object is then reconstructed on a computer. However, the pinhole aperture approach has a disadvantage. In order to produce a sharp image, the aperture must be very small, which therefore transmits too little light to create a good image from low-contrast objects or during short exposure times – a dilemma.

Physicists working with Eisebitt found a solution by using an optical element known as a Fresnel zone plate. This is placed in the plane of the object itself as a substitute for the pinhole aperture and considerably increases the brightness of the reference wave. However, the focal point of this optical element is not in the plane of the object (as the pinhole aperture would be), so that the image is out of focus. In contrast to photography, however, this blur in the image can be precisely corrected for via the information stored in the hologram. Due to the efficiency of the method, exposure times can be significantly reduced, allowing the study of fast dynamic processes.

This is  a test sample image,

The outline of the lizard serves as a test object, as well as the conventional test pattern, a section of a so called Siemens star. The lizard’s tail and the converging rays of the Siemens star can be used to measure how well narrow lines will be reproduced in an image. With a diameter of six thousandths of a millimetre, the entire test object is about the size of a red blood cell. The smallest resolved structure has a width of 46 nanometres. Credit: J. Geilhufe/HZB

The outline of the lizard serves as a test object, as well as the conventional test pattern, a section of a so called Siemens star. The lizard’s tail and the converging rays of the Siemens star can be used to measure how well narrow lines will be reproduced in an image. With a diameter of six thousandths of a millimetre, the entire test object is about the size of a red blood cell. The smallest resolved structure has a width of 46 nanometres. Credit: J. Geilhufe/HZB

The press release explains what we’re actually looking at,

Ph.D. student Jan Geilhufe worked out this idea and implemented it. He was also the one who introduced the image of a lizard as a filigreed test object. Its outline was reduced by a factor of 10,000 and transferred onto gold foil. “It was important to us to find a test object with some originality for demonstrating how well the method works”, says Geilhufe. The seashell in the centre of the test object displays a section of what is called a Siemens star, a test pattern used to determine spatial resolution. Similar to how the converging rays of a Siemens star can be used to measure how well narrow lines will be reproduced in an image, you can also use the lizard’s tail. With a diameter of six thousandths of a millimetre, the entire test object is about the size of a red blood cell. The smallest resolved structure has a width of no more than 46 nanometres.

As for the jitter I mentioned in the headline (from the press release),

The well-known problem of jitter due to vibrations of the object in relation to the optics becomes increasingly dramatic at higher resolution of an optical system. “In current research for high-resolution X-ray imaging, a resolution of less than ten nanometres is the target. That distance is tiny – less than a chain of one hundred single atoms. For that reason, even the smallest fluctuations are noticeable. A streetcar passing by a kilometre away can be a disturbance”, says Geilhufe. “In our process, we have firmly coupled the object to the reference optics so that the lens fluctuates exactly synchronized with the object. We have built an X-ray camera with an image stabiliser, so to speak.”

The work is being published today in Nature Communications. The improvement in imaging efficiency and resulting possibilities for improvement in spatial and temporal resolution promises new insights into dynamic nanoscale processes, such as fastest magnetic switching in data storage. “We hope that our approach is useful for many areas of research and contributes to understanding the world at the nanometre scale”, says Eisebitt. He and his team are looking forward to offering their new holographic technique to researchers from all over the world at BESSY II as part of the RICXS instrument.

Here’s a link to and a citation for the paper,

Monolithic focused reference beam X-ray holography by J. Geilhufe, B. Pfau, M. Schneider, F. Büttner, C. M. Günther, S. Werner, S. Schaffert, E. Guehrs, S. Frömmel, M. Kläui, & S. Eisebitt. Nature Communications 5, Article number: 3008 doi:10.1038/ncomms4008 Published 07 January 2014

This paper is open access.

Nanodiamonds as imaging devices

Two different teams have recently published studies in Science magazine (Feb. 1, 2013 issue) about their work with nanodiamonds, flaws, and imaging in what seems to be a case of synchronicity as there are no obvious connections between the teams.

Sabrina Richards writes in her Jan. 31, 2013 article for The Scientist about the possibility of taking snapshots of molecules at some time in the future (Note: Links have been removed),

A miniscule diamond flaw—just two atoms different—could someday enable researchers to image single molecules without resorting to time-consuming and technically exacting X-ray crystallography. The new approach, published today (January 31 [sic]) in Science, relies on a single electron to detect perturbation in molecular magnetic fields, which can provide clues about the structures of proteins and other molecules.

The work was inspired by magnetic resonance imaging (MRI), which uses electromagnetic coils to detect the magnetic fields emitted by hydrogen atom protons.  But traditional MRI requires many trillions of protons to get a clear image—of a brain, for example—preventing scientists from visualizing anything much smaller than millimeters-wide structures. To detect just a few protons, such as those of a single molecule, scientists would need an atomic-scale sensor.

To construct such a sensor, physicists Daniel Rugar at IBM Research and David Awschalom at the University of California, Santa Barbara, turned to diamonds. A perfect diamond, made entirely of carbon atoms covalently bonded to each other, has no free electrons and therefore no magnetic properties, explained Hammel. But a special kind of defect, known as a nitrogen-vacancy (NV) center, confers unique magnetic properties.

Jyllian Kemsley’s Jan. 31, 2013 article for C&EN (Chemical and Engineering News) discusses the work from both teams and describes the technique they used,

To downscale NMR [aka MRI], both groups used a detector made of diamond with a site defect called a single nitrogen-vacancy (NV) center, in which a nitrogen atom and a lattice hole replace two adjacent carbon atoms. Prior work had determined that NV centers are sensitive to the internal magnetic fields of the diamond. The new research demonstrates that the fluorescence of such centers can be used to detect magnetic fields emanating from just outside the diamond. Both groups were able to use NV centers to detect nuclear polarization of hydrogens in poly(methyl methacrylate) with a sample volume lower limit of about (5 nm)3. Further development is necessary to extract structural information.

Still, nothing much has happened with this technique as Richards notes in her article,

So far, the study is “just a proof of principle,” noted Awschalom. The researchers haven’t actually imaged any molecules yet, but simply detected their presence. Still, Awschalom said, “we’ve shown it’s not a completely ridiculous idea to detect external nuclear magnetic fields with one electron.” …

Here’s a citation and a link to the article,

Nanoscale Nuclear Magnetic Resonance with a Nitrogen-Vacancy Spin Sensor by H. J. Mamin, M. Kim, M. H. Sherwood, C. T. Rettner, K. Ohno, D. D. Awschalom, D. Rugar. Science 1 February 2013: Vol. 339 no. 6119 pp. 557-560 DOI: 10.1126/science.1231540

The other research is described in a Feb. 14, 2013 news item on Azonano,

Magnetic resonance imaging (MRI) reveals details of living tissues, diseased organs and tumors inside the body without x-rays or surgery. What if the same technology could peer down to the level of atoms? Doctors could make visual diagnoses of a person’s molecules – examining damage on a strand of DNA, watching molecules misfold, or identifying a cancer cell by the proteins on its surface.

It is remarkably  similar work as Kemsley notes not helped by the fact that the one line description for both articles in Science magazine’s Table of Contents is identical.  (One line description: The optical response of the spin of a near-surface atomic defect in diamond can be used to sense proton magnetic fields.) The City College of New York City Feb. 13, 2013 news release, which originated the Azonano news item about the other team, offers more details,

 … Dr. Carlos Meriles, associate professor of physics at The City College of New York, and an international team of researchers at the University of Stuttgart and elsewhere have opened the door for nanoscale MRI. They used tiny defects in diamonds to sense the magnetic resonance of molecules. They reported their results in the February 1 [2013] issue of Science.

“It is bringing MRI to a level comparable to an atomic force microscope,” said Professor Meriles, referring to the device that traces the contours of atoms or tugs on a molecule to measure its strength. A nanoscale MRI could display how a molecule moves without touching it.

“Standard MRI typically gets to a resolution of 100 microns,” about the width of a human hair, said Professor Meriles. “With extraordinary effort,” he said, “it can get down to about 10 microns” – the width of a couple of blood cells. Nanoscale MRI would have a resolution 1,000 to 10,000 times better.

To try to pick up magnetic resonance on such a small scale, the team took advantage of the spin of protons in an atom, a property usually used to investigate quantum computing. In particular, they used minute imperfections in diamonds.

Diamonds are crystals made up almost entirely of carbon atoms. When a nitrogen atom lodges next to a spot where a carbon atom is missing, however, it creates a defect known as a nitrogen-vacancy (NV) center.

“These imperfections turn out to have a spin – like a little compass – and have some remarkable properties,” noted Professor Meriles. In the last few years, researchers realized that these NV centers could serve as very sensitive sensors. They can pick up the magnetic resonance of nearby atoms in a cell, for example. But unlike the atoms in a cell, the NVs shine when a light is directed at them, signaling what their spin is. If you illuminate it with green light it flashes red back.

“It is a form of what is called optically detected magnetic resonance,” he said. Like a hiker flashing Morse code on a hillside, the sensor “sends back flashes to say it is alive and well.”

“The NV can also be thought of as an atomic magnet. You can manipulate the spin of that atomic magnet just like you do with MRI by applying a radio frequency or radio pulses,” Professor Meriles explained. The NV responds. Shine a green light at it when the spin is pointing up and it will respond with brighter red light. A down spin gives a dimmer red light.

In the lab, graduate student Tobias Staudacher — the first author in this work — used NVs that had been created just below the diamond’s surface by bombarding it with nitrogen atoms. The team detected magnetic resonance within a film of organic material applied to the surface, just as one might examine a thin film of cells or tissue.

“Ultimately,” said Professor Meriles, “One will use a nitrogen-vacancy mounted on the tip of an atomic force microscope – or an array of NVs distributed on the diamond surface – to allow a scanning view of a cell, for example, to probe nuclear spins with a resolution down to a nanometer or perhaps better.”

Here’s a citation and a link to this team’s study,

Nuclear Magnetic Resonance Spectroscopy on a (5-Nanometer)3 Sample Volume by T. Staudacher, F. Shi, S. Pezzagna, J. Meijer, J. Du, C. A. Meriles, F. Reinhard1, J. Wrachtrup. Science 1 February 2013: Vol. 339 no. 6119 pp. 561-563 DOI: 10.1126/science.1231675

Both articles are behind paywalls.