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The same electrostatic charge that can make hair stand on end and attach balloons to clothing could be an efficient way to drive atomically thin electronic memory devices of the future, according to a new study led by researchers at the Department of Energy’s Lawrence Berkeley National Laboratory (Berkeley Lab).

In a study published today in the journal Nature, scientists have found a way to reversibly change the atomic structure of a 2-D material by injecting, or “doping,” it with electrons. The process uses far less energy than current methods for changing the configuration of a material’s structure.

Schematic shows the configuration for structural phase transition on a molybdenum ditelluride monolayer (MoTe2, shown as yellow and blue spheres), which is anchored by a metal electrodes (top gate and ground). The ionic liquid covering the monolayer and electrodes enables a high density of electrons to populate the monolayer, leading to changes in the structural lattice from a hexagonal (2H) to monoclinic (1T') pattern. Credit: Ying Wang/Berkeley Lab

Schematic shows the configuration for structural phase transition on a molybdenum ditelluride monolayer (MoTe2, shown as yellow and blue spheres), which is anchored by a metal electrodes (top gate and ground). The ionic liquid covering the monolayer and electrodes enables a high density of electrons to populate the monolayer, leading to changes in the structural lattice from a hexagonal (2H) to monoclinic (1T’) pattern. Credit: Ying Wang/Berkeley Lab

“We show, for the first time, that it is possible to inject electrons to drive structural phase changes in materials,” said study principal investigator Xiang Zhang, senior faculty scientist at Berkeley Lab’s Materials Sciences Division and a professor at UC Berkeley. “By adding electrons into a material, the overall energy goes up and will tip off the balance, resulting in the atomic structure re-arranging to a new pattern that is more stable. Such electron doping-driven structural phase transitions at the 2-D limit is not only important in fundamental physics; it also opens the door for new electronic memory and low-power switching in the next generation of ultra-thin devices.”

Switching a material’s structural configuration from one phase to another is the fundamental, binary characteristic that underlies today’s digital circuitry. Electronic components capable of this phase transition have shrunk down to paper-thin sizes, but they are still considered to be bulk, 3-D layers by scientists. By comparison, 2-D monolayer materials are composed of a single layer of atoms or molecules whose thickness is 100,000 times as small as a human hair.

“The idea of electron doping to alter a material’s atomic structure is unique to 2-D materials, which are much more electrically tunable compared with 3-D bulk materials,” said study co-lead author Jun Xiao, a graduate student in Zhang’s lab.

The classic approach to driving the structural transition of materials involves heating to above 500 degrees Celsius. Such methods are energy-intensive and not feasible for practical applications. In addition, the excess heat can significantly reduce the life span of components in integrated circuits.

A number of research groups have also investigated the use of chemicals to alter the configuration of atoms in semiconductor materials, but that process is still difficult to control and has not been widely adopted by industry.

“Here we use electrostatic doping to control the atomic configuration of a two-dimensional material,” said study co-lead author Ying Wang, another graduate student in Zhang’s lab. “Compared to the use of chemicals, our method is reversible and free of impurities. It has greater potential for integration into the manufacturing of cell phones, computers and other electronic devices.”

The researchers used molybdenum ditelluride (MoTe2), a typical 2-D semiconductor, and coated it with an ionic liquid (DEME-TFSI), which has an ultra-high capacitance, or ability to store electric charges. The layer of ionic liquid allowed the researchers to inject the semiconductor with electrons at a density of a hundred trillion to a quadrillion per square centimeter. It is an electron density that is one to two orders higher in magnitude than what could be achieved in 3-D bulk materials, the researchers said.

Through spectroscopic analysis, the researchers determined that the injection of electrons changed the atoms’ arrangement of the molybdenum ditelluride from a hexagonal shape to one that is monoclinic, which has more of a slanted cuboid shape. Once the electrons were retracted, the crystal structure returned to its original hexagonal pattern, showing that the phase transition is reversible. Moreover, these two types of atom arrangements have very different symmetries, providing a large contrast for applications in optical components.

“Such an atomically thin device could have dual functions, serving simultaneously as optical or electrical transistors, and hence broaden the functionalities of the electronics used in our daily lives,” said Wang.

A team led by Cory Dean, assistant professor of physics at Columbia University, and James Hone, Wang Fong-Jen Professor of Mechanical Engineering at Columbia Engineering, has definitively observed an intensely studied anomaly in condensed matter physics—the even-denominator fractional quantum Hall (FQH) state—via transport measurement in bilayer graphene. The study is published online in Science (October 6 issue).

“Observing the 5/2 state in any system is a remarkable scientific opportunity, since it encompasses some of the most perplexing concepts in modern condensed matter physics, such as emergence, quasi-particle formation, quantization, and even superconductivity,” Dean says. “Our observation that, in bilayer graphene, the 5/2 state survives to much higher temperatures than previously thought possible not only allows us to study this phenomenon in new ways, but also shifts our view of the FQH state from being largely a scientific curiosity to now having great potential for real-world applications, particularly in quantum computing.”

First discovered in the 1980s in gallium arsenide (GaAs) heterostructures, the 5/2 fractional quantum hall state remains the singular exception to the otherwise strict rule that says fractional quantum hall states can only exist with odd denominators. Soon after the discovery, theoretical work suggested that this state could represent an exotic type of superconductor, notable in part for the possibility that such a phase could enable a fundamentally new approach to quantum computation. However, confirmation of these theories has remained elusive, largely due to the fragile nature of the state; in GaAs it is observable only in the highest quality samples and even then appearing only at milikelvin temperaures (as much as 10,000 times colder than the freezing point of water).

The Columbia team has now observed this same state in bilayer graphene and appearing at much higher temperatures¾reaching several Kelvin. “While it’s still 100 times colder than the freezing point of water, seeing the even-denominator state at these temperatures opens the door to a whole new suite of experimental tools that previously were unthinkable,” says Dean. “After several decades of effort by researchers all over the world, we may finally be close to solving the mystery of the 5/2.”

One of the outstanding problems in the field of modern condensed matter physics is understanding the phenomenon of “emergence,” the result of a large collection of quantum particles behaving in concert due to interactions between the particles and giving rise to new characteristics that are not a feature of the individual parts. For instance, in superconductors, a large number of electrons all collapse to a single quantum state, which can then propagate through a metal without any energy loss. The fractional quantum Hall effect is another state in which electrons collude with one another, in the presence of a magnetic field, resulting in quasiparticles with potentially exotic quantum properties.

Very difficult to predict theoretically, emergence often challenges our foundational understanding of how particles behave. For example, since any two electrons have the same charge, we think of electrons as objects that want to repel each other. However, in a superconducting metal, electrons unexpectedly pair up, forming a new object known as a cooper pair. Individual electrons scatter when moving through a metal, giving rise to resistance, but spontaneously formed cooper pairs behave collectively in such a way that they move through the material with no resistance at all.

“Think of trying to make your way through a crowd at a rock concert where everyone is dancing with a lot of energy and constantly bumping into you, compared to a ballroom dance floor where pairs of dancers are all moving in the same, carefully choreographed way, and it is easy to avoid each other,” says Dean. “One of the reasons that makes the even-denominator fractional quantum Hall effect so fascinating is that its origin is believed to be very similar to that of a superconductor, but, instead of simply forming cooper pairs, an entirely new kind of quantum particle emerges.”

According to quantum mechanics, elementary particles fall into two categories, Fermions and Bosons, and behave in very different ways. Two Fermions, such as electrons, cannot occupy the same state, which is why, for example, the electrons in atoms fill successive orbitals. Bosons, such as photons, or particles of light, can occupy the same state, allowing them to act coherently as in the light emission from a laser. When two identical particles are interchanged, the quantum mechanical wave-function describing their combined state is multiplied by a phase factor of 1 for Bosons, and -1 for Fermions.

Soon after the discovery of the fractional quantum hall effect, it was suggested on theoretical grounds that the quasiparticles associated with this state behave neither as Bosons nor Fermions but instead what is called an anyon: when anyon quasiparticles are interchanged, the phase factor is neither 1 nor -1 but is fractional. Despite several decades of effort, there still is no conclusive experimental proof confirming that these quasiparticles are anyons. The 5/2 state¾-a non-abelian anyon¾-is thought to be even more exotic. In theory, non-abelian anyons obey anyonic statistics as in other fractional quantum Hall states, but with the special feature that this phase cannot simply be undone by reversing the process. This inability to simply unwind the phase would make any information stored in the system uniquely stable, and is why many people believe the 5/2 could be a great candidate for quantum computation.

“Demonstration of the predicted 5/2 statistics would represent a tremendous achievement,” says Dean. “In many regards, this would confirm that, by fabricating a material system with just the right thickness and just the right number of electrons, and then applying just the right magnetic fields, we could effectively engineer fundamentally new classes of particles, with properties that do not otherwise exist among known particles naturally found in the universe. We still have no conclusive evidence that the 5/2 state exhibits non-abelian properties, but our discovery of this state in bilayer graphene opens up exciting new opportunities to test these theories.”

Until now, all of those conditions have needed to be not only just right but also extreme. In conventional semi-conductors, the even-denominator states are very difficult to isolate, and exist only for ultra-pure materials, at extremely low temperatures and high magnetic fields. While certain features of the state have been observable devising experiments that could investigate the state without destroying it, has been challenging.

“We needed a new platform,” says Hone. “With the successful isolation of graphene, these atomically thin layers of carbon atoms emerged as a promising platform for the study of electrons in 2D in general. One of the keys is that electrons in graphene interact even more strongly than in conventional 2D electron systems, theoretically making effects such as the even-denominator state even more robust. But while there have been predictions that bilayer graphene could host the long-sought even-denominator states, at higher temperatures than seen before, these predictions have not been realized due mostly the difficulty of making graphene clean enough.”

The Columbia team built on many years of pioneering work to improve the quality of graphene devices, creating ultra-clean devices entirely from atomically flat 2D materials: bilayer graphene for the conducting channel, hexagonal boron nitride as a protective insulator, and graphite used for electrical connections and as a conductive gate to change the charge carrier density in the channel.
A crucial component of the research was having access to the high magnetic fields tools available at the National High Magnetic Field Laboratory in Tallahassee, Fla., a nationally funded user facility with which Hone and Dean have had extensive collaborations. They studied the electrical conduction through their devices under magnetic fields up to 34 Tesla, and achieved clear observation of the even-denominator states.

“By tilting the sample with respect to the magnetic field, we were able to provide new confirmation that this FQH state has many of the properties predicted by theory, such as being spin-polarized,” says Jia Li, the paper’s lead author and post-doctoral researcher working with Dean and Hone. “We also discovered that in bilayer graphene, this state can be manipulated in ways that are not possible in conventional materials.”

The Columbia team’s result, which demonstrates measurement in transport—how electrons flow in the system—is a crucial step forward towards confirming the possible exotic origin of the even denominator state. Their findings are reported contemporaneously with a similar report by a research group at University of California, Santa Barbara. The UCSB study observed the even denominator state by capacitance measurement, which probes the existence of an electrical gap associated with the onset of the state.

The team expects that the robust measurements they have now observed in bilayer graphene will enable new experiments that could definitively prove its non-abelian nature. Once this is established, the team hopes to begin demonstrating computation using the even denominator state.

“For many decades now it has been thought that if the 5/2 state does indeed represent a non-abelian anyon, it could theoretically revolutionize efforts to build a quantum computer,” Dean observes. “In the past, however, the extreme conditions necessary to see the state at all, let alone use it for computation, were always a major concern of practicality. Our results in bilayer graphene suggest that this dream may now not actually be so far from reality.”

Physicists at the University of California, Riverside have developed a photodetector – a device that senses light – by combining two distinct inorganic materials and producing quantum mechanical processes that could revolutionize the way solar energy is collected.

Photodetectors are almost ubiquitous, found in cameras, cell phones, remote controls, solar cells, and even the panels of space shuttles. Measuring just microns across, these tiny devices convert light into electrons, whose subsequent movement generates an electronic signal. Increasing the efficiency of light-to-electricity conversion has been one of the primary aims in photodetector construction since their invention.

Lab researchers stacked two atomic layers of tungsten diselenide (WSe2) on a single atomic layer of molybdenum diselenide (MoSe2). Such stacking results in properties vastly different from those of the parent layers, allowing for customized electronic engineering at the tiniest possible scale.

This image shows an energy diagram of the WSe2-MoSe2 device. When a photon (1) strikes the WSe2 layer, it knocks loose an electron (2), freeing it to conduct through the WSe2 (3). At the junction between the two materials, the electron drops down into MoSe2 (4). The energy given off in the drop catapults a second electron from the WSe2 (5) into the MoSe2 (6), where both electrons are free to move and generate electricity. Credit: University Communications, UC Riverside.

This image shows an energy diagram of the WSe2-MoSe2 device. When a photon (1) strikes the WSe2 layer, it knocks loose an electron (2), freeing it to conduct through the WSe2 (3). At the junction between the two materials, the electron drops down into MoSe2 (4). The energy given off in the drop catapults a second electron from the WSe2 (5) into the MoSe2 (6), where both electrons are free to move and generate electricity. Credit: University Communications, UC Riverside.

Within atoms, electrons live in states that determine their energy level. When electrons move from one state to another, they either acquire or lose energy. Above a certain energy level, electrons can move freely. An electron moving into a lower energy state can transfer enough energy to knock loose another electron.

UC Riverside physicists observed that when a photon strikes the WSe2 layer, it knocks loose an electron, freeing it to conduct through the WSe2. At the junction between WSe2 and MoSe2, the electron drops down into MoSe2. The energy given off then catapults a second electron from the WSe2 into the MoSe2, where both electrons become free to move and generate electricity.

“We are seeing a new phenomenon occurring,” said Nathaniel M. Gabor, an assistant professor of physics, who led the research team. “Normally, when an electron jumps between energy states, it wastes energy. In our experiment, the waste energy instead creates another electron, doubling its efficiency. Understanding such processes, together with improved designs that push beyond the theoretical efficiency limits, will have a broad significance with regard to designing new ultra-efficient photovoltaic devices.”

Study results appear today in Nature Nanotechnology.

“The electron in WSe2 that is initially energized by the photon has an energy that is low with respect to WSe2,” said Fatemeh Barati, a graduate student in Gabor’s Quantum Materials Optoelectronics lab and the co-first author of the research paper. “With the application of a small electric field, it transfers to MoSe2, where its energy, with respect to this new material, is high. Meaning, it can now lose energy. This energy is dissipated as kinetic energy that dislodges the additional electron from WSe2.”

In existing solar panels models, one photon can at most generate one electron. In the prototype the researchers developed, one photon can generate two electrons or more through a process called electron multiplication.

The researchers explained that in ultrasmall materials, electrons behave like waves. Though it is unintuitive at large scales, the process of generating two electrons from one photon is perfectly allowable at extremely small length scales. When a material, such as WSe2 or MoSe2, gets thinned down to dimensions nearing the electron’s wavelength, the material’s properties begin to change in inexplicable, unpredictable, and mysterious ways.

“It’s like a wave stuck between walls closing in,” Gabor said. “Quantum mechanically, this changes all the scales. The combination of two different ultra small materials gives rise to an entirely new multiplication process. Two plus two equals five.”

“Ideally, in a solar cell we would want light coming in to turn into several electrons,” said Max Grossnickle, also a graduate student in Gabor’s lab and the research paper’s co-first author. “Our paper shows that this is possible.”

Barati noted that more electrons could be generated also by increasing the temperature of the device.

“We saw a doubling of electrons in our device at 340 degrees Kelvin (150 F), which is slightly above room temperature,” she said. “Few materials show this phenomenon around room temperature. As we increase this temperature, we should see more than a doubling of electrons.”

Electron multiplication in conventional photocell devices typically requires applied voltages of 10-100 volts. To observe the doubling of electrons, the researchers used only 1.2 volts, the typical voltage supplied by an AA battery.

“Such low voltage operation, and therefore low power consumption, may herald a revolutionary direction in photodetector and solar cell material design,” Grossnickle said.

He explained that the efficiency of a photovoltaic device is governed by a simple competition: light energy is either converted into waste heat or useful electronic power.

“Ultrathin materials may tip the balance in this competition by simultaneously limiting heat generation, while increasing electronic power,” he said.

Gabor explained that the quantum mechanical phenomenon his team observed in their device is similar to what occurs when cosmic rays, coming into contact with the Earth’s atmosphere with high kinetic energy, produce an array of new particles.

He speculated that the team’s findings could find applications in unforeseen ways.

“These materials, being only an atom thick, are nearly transparent,” he said. “It’s conceivable that one day we might see them included in paint or in solar cells incorporated into windows. Because these materials are flexible, we can envision their application in wearable photovoltaics, with the materials being integrated into the fabric. We could have, say, a suit that generates power – energy-harvesting technology that would be essentially invisible.”

A sea of spinning electrons


October 3, 2017

Picture two schools of fish swimming in clockwise and counterclockwise circles. It’s enough to make your head spin, and now scientists at Rutgers University-New Brunswick and the University of Florida have discovered the “chiral spin mode” – a sea of electrons spinning in opposing circles.

“We discovered a new collective spin mode that can be used to transport energy or information with very little energy dissipation, and it can be a platform for building novel electronic devices such as computers and processors,” said Girsh Blumberg, senior author of the study and a professor in the Department of Physics and Astronomy in Rutgers’ School of Arts and Sciences.

Collective chiral spin modes are propagating waves of electron spins that do not carry a charge current but modify the “spinning” directions of electrons. “Chiral” refers to entities, like your right and left hands, that are matching but asymmetrical and can’t be superimposed on their mirror image.

The study, led by Hsiang-Hsi (Sean) Kung, a graduate student in Blumberg’s Rutgers Laser Spectroscopy Lab, was published in Physical Review Letters. Kung used a custom-made, ultra-sensitive spectrometer to study a prototypical 3D topological insulator. A microscopic theoretical model that predicts the energy and temperature evolution of the chiral spin mode was developed by Saurabh Maiti and Professor Dmitrii Maslov at the University of Florida, strongly substantiating the experimental observation.

The blue and red cones show the energy and momentum of surface electrons in a 3D topological insulator. The spin structure is shown in the blue and red arrows at the top and bottom, respectively. Light promotes electrons from the blue cone into the red cone, with the spin direction flipping. The orderly spinning leads to the chiral spin mode observed in this study. Credit: Hsiang-Hsi (Sean) Kung/Rutgers University-New Brunswick

The blue and red cones show the energy and momentum of surface electrons in a 3D topological insulator. The spin structure is shown in the blue and red arrows at the top and bottom, respectively. Light promotes electrons from the blue cone into the red cone, with the spin direction flipping. The orderly spinning leads to the chiral spin mode observed in this study.
Credit: Hsiang-Hsi (Sean) Kung/Rutgers University-New Brunswick

In a vacuum, electrons are simple, boring elementary particles. But in solids, the collective behavior of many electrons interacting with each other and the underlying platform may result in phenomena that lead to new applications in superconductivity, magnetism and piezoelectricity (voltage generated via materials placed under pressure), to name a few. Condensed matter science, which focuses on solids, liquids and other concentrated forms of matter, seeks to reveal new phenomena in new materials.

Silicon-based electronics, such as computer chips and computers, are one of the most important inventions in human history. But silicon leads to significant energy loss when scaled down. One alternative is to harness the spins of electrons to transport information through extremely thin wires, which in theory would slash energy loss.

The newly discovered “chiral spin mode” stems from the sea of electrons on the surface of “3D topological insulators.” These special insulators have nonmagnetic, insulating material with robust metallic surfaces, and the electrons are confined so they move only on 2D surfaces.

Most importantly, the electrons’ spinning axes are level and perpendicular to their velocity. Chiral spin modes emerge naturally from the surface of such insulating materials, but they were never observed before due to crystalline defects. The experimental observation in the current study was made possible following the development of ultra-clean crystals by Rutgers doctoral student Xueyun Wang and Board of Governors Professor Sang-Wook Cheong in the Rutgers Center for Emergent Materials.

The discovery paves new paths for building next generation low-loss electronic devices.

Graphene is a sheet of carbon that is only one atom thick, and it has drawn worldwide attention as a new material. A research group from Kumamoto University, Japan has discovered that pressure can be generated by simply stacking graphene oxide nanosheets, a material that closely resembles graphene. They also found that the pressure can be increased by reducing the interlayer distance through heat treatment. It is an innovative approach for applying high pressure without using an enormous amount of energy.

The 2010 Nobel Prize in Physics was awarded to two scientists, Andre Geim and Konstantin Novoselov, for groundbreaking graphene experiments. The carbon material is very thin, strong, flexible, and has high electrical conductivity. Oxidized graphene nanosheets have many oxygen functional groups at the front and back of graphene, and previous research has shown that if several layers of oxidized graphene nanosheets are heat treated, the interlayer distance shrinks as oxygen functional groups are eliminated.

This led the researchers at Kumamoto University, Japan to consider that reducing the interlayer distance of graphene oxide nanosheets, could allow it to be used as a compressor that applies pressure to a substance sandwiched between the sheets. To measure pressure between nanosheets, they used molecular materials that change the electrical state of metal ions in response to pressure (spin crossover phenomenon). They observed an electrical state change of iron nanoparticles by sandwiching the material and measuring the spin crossover phenomenon between graphene oxide nanosheets.

As the interlayer distance becomes smaller, the pressure between layers rises. This means that the pressure value can be adjusted by the heat treatment temperature. The maximum pressure the researchers measured was 38 x 106 Pa (101,300 Pa at atmospheric pressure, or about 375 atm). Moreover, they found that pressure does not occur unless the nanosheets are properly stacked.

“There are several examples of special materials that cause compression by just sandwiching or wrapping, similar to our results here,” said Assistant Professor Ryo Ohtani of Kumamoto University, who led the study. “But, as far as we know, this graphene nanosheet is the first example in the world with the ability to adjust applied pressure by simply changing the heat treatment temperature. We expect that this “nano-compressor” will lead to new developments from fields such as material chemistry or physics. Particularly since this technique produces high pressures that normally cannot be obtained without adding a large amount of energy.”

Researchers from Finland and Taiwan have discovered how graphene, a single-atom-thin layer of carbon, can be forged into three-dimensional objects by using laser light. A striking illustration was provided when the researchers fabricated a pyramid with a height of 60nm, which is about 200 times larger than the thickness of a graphene sheet. The pyramid was so small that it would easily fit on a single strand of hair. The research was supported by the Academy of Finland and the Ministry of Science and Technology of the Republic of China.

A similar structure was made experimentally by using laser irradiation in a process called "optical forging." Credit: The University of Jyväskylä

A similar structure was made experimentally by using laser irradiation in a process called “optical forging.” Credit: The University of Jyväskylä

Graphene is a close relative to graphite, which consists of millions of layers of graphene and can be found in common pencil tips. After graphene was first isolated in 2004, researchers have learned to routinely produce and handle it. Graphene can be used to make electronic and optoelectronic devices, such as transistors, photodetectors and sensors. In future, we will probably see an increasing number of products containing graphene.

“We call this technique optical forging, since the process resembles forging metals into 3D shapes with a hammer. In our case, a laser beam is the hammer that forges graphene into 3D shapes,” explains Professor Mika Pettersson, who led the experimental team at the Nanoscience Center of the University of Jyväskylä, Finland. “The beauty of the technique is that it’s fast and easy to use; it doesn’t require any additional chemicals or processing. Despite the simplicity of the technique, we were very surprised initially when we observed that the laser beam induced such substantial changes on graphene. It took a while to understand what was happening.”

“At first, we were flabbergasted. The experimental data simply made no sense,” says Dr Pekka Koskinen, who was responsible for the theory. “But gradually, by close interplay between experiments and computer simulations, the actuality of 3D shapes and their formation mechanism started to become clear.”

“When we first examined the irradiated graphene, we were expecting to find traces of chemical species incorporated into the graphene, but we couldn’t find any. After some more careful inspections, we concluded that it must be purely structural defects, rather than chemical doping, that are responsible for such dramatic changes on graphene,” explains Associate Professor Wei Yen Woon from Taiwan, who led the experimental group that carried out X-ray photoelectron spectroscopy at the synchrotron facility.

The novel 3D graphene is stable and it has electronic and optical properties that differ from normal 2D graphene. Optically forged graphene can help in fabricating 3D architectures for graphene-based devices.

A research group consisting of scientists from Tomsk Polytechnic University, Germany and Venezuela proved vulnerability of a two-dimensional semiconductor gallium selenide in air. This discovery will allow manufacturing superconducting nanoelectronics based on gallium selenide, which has never been previously achieved by any research team in the world.

The study was published in Semiconductor Science and Technology.

One of the promising areas of modern materials science is the study of two-dimensional (2D) materials, i.e. thin films consisting of one or several atomic layers. 2D materials due to their electrical superconductivity and strength could be a basis for modern nanoelectronics. Optic applications in nanoelectronics require advanced materials capable of ‘generating’ great electron fluxes upon light irradiation. Gallium selenide (GaSe) is one of the 2D semiconductors that can cope with this problem most efficiently.

‘Some research teams abroad tried to create electronic devices based on GaSe. However, despite extensive theoretical studies of this material, which were published in major scientific journals, the stability of the material in real devices remained unclear,’ says Prof. Raul Rodriguez, the Department of Lasers and Lighting Engineering.

The research team revealed the reasons behind this. They studied GaSe by means of Raman spectroscopy and x-ray photoelectron spectroscopy that allowed proving the existence of chemical bonds between gallium and oxygen. Photoluminescence in oxidized substance is absent that also proves the formation of oxides. It means that the scientists revealed that GaSe oxidizes quickly in air and loses its electrical conductivity necessary for creating nanoeletronic devices.

‘GaSe monolayers become oxidized almost immediately after being exposed to air. Further research of GASe stability in air will allow making proposals how to protect it and maintain its optoelectronic properties,’ emphasize the authors.

According to Prof. Rodriguez, for GaSe not to lose its unique properties it should be placed in a vacuum or inert environment. For example, it can be applied in encapsulated devices that are vacuum-manufactured and then covered with a protective layer eliminating air penetration.

This method can be used to produce next generation optoelectronics, detectors, light sources and solar batteries. Such devices of ultra-small sizes will have very high quantum efficiency, i.e. they will be able to generate large electron fluxes under small external exposure.

Scarce metals are found in a wide range of everyday objects around us. They are complicated to extract, difficult to recycle and so rare that several of them have become “conflict minerals” which can promote conflicts and oppression. A survey at Chalmers University of Technology now shows that there are potential technology-based solutions that can replace many of the metals with carbon nanomaterials, such as graphene.

They can be found in your computer, in your mobile phone, in almost all other electronic equipment and in many of the plastics around you. Society is highly dependent on scarce metals, and this dependence has many disadvantages.

Scarce metals such as tin, silver, tungsten and indium are both rare and difficult to extract since the workable concentrations are very small. This ensures the metals are highly sought after – and their extraction is a breeding ground for conflicts, such as in the Democratic Republic of the Congo where they fund armed conflicts.

In addition, they are difficult to recycle profitably since they are often present in small quantities in various components such as electronics.

Rickard Arvidsson and Björn Sandén, researchers in environmental systems analysis at Chalmers University of Technology, have now examined an alternative solution: substituting carbon nanomaterials for the scarce metals. These substances – the best known of which is graphene – are strong materials with good conductivity, like scarce metals.

“Now technology development has allowed us to make greater use of the common element carbon,” says Sandén. “Today there are many new carbon nanomaterials with similar properties to metals. It’s a welcome new track, and it’s important to invest in both the recycling and substitution of scarce metals from now on.”

The Chalmers researchers have studied the main applications of 14 different metals, and by reviewing patents and scientific literature have investigated the potential for replacing them by carbon nanomaterials. The results provide a unique overview of research and technology development in the field.

According to Arvidsson and Sandén the summary shows that a shift away from the use of scarce metals to carbon nanomaterials is already taking place.

“There are potential technology-based solutions for replacing 13 out of the 14 metals by carbon nanomaterials in their most common applications. The technology development is at different stages for different metals and applications, but in some cases such as indium and gallium, the results are very promising,” Arvidsson says.

“This offers hope,” says Sandén. “In the debate on resource constraints, circular economy and society’s handling of materials, the focus has long been on recycling and reuse. Substitution is a potential alternative that has not been explored to the same extent and as the resource issues become more pressing, we now have more tools to work with.”

The research findings were recently published in the Journal of Cleaner Production. Arvidsson and Sandén stress that there are significant potential benefits from reducing the use of scarce metals, and they hope to be able to strengthen the case for more research and development in the field.

“Imagine being able to replace scarce metals with carbon,” Sandén says. “Extracting the carbon from biomass would create a natural cycle.”

“Since carbon is such a common and readily available material, it would also be possible to reduce the conflicts and geopolitical problems associated with these metals,” Arvidsson says.

At the same time they point out that more research is needed in the field in order to deal with any new problems that may arise if the scarce metals are replaced.

“Carbon nanomaterials are only a relatively recent discovery, and so far knowledge is limited about their environmental impact from a life-cycle perspective. But generally there seems to be a potential for a low environmental impact,” Arvidsson says.

Facts:

Carbon nanomaterials consist solely or mainly of carbon, and are strong materials with good conductivity. Several scarce metals have similar properties. The metals are found, for example, in cables, thin screens, flame-retardants, corrosion protection and capacitors.

Rickard Arvidsson and Björn Sandén at Chalmers University of Technology have investigated whether the carbon nanomaterials graphene, fullerenes and carbon nanotubes have the potential to replace 14 scarce metals in their main areas of application (see table in attached image). They found potential technology-based solutions to replace the metals with carbon nanomaterials for all applications except for gold in jewellery. The metals which we are closest to being able to substitute are indium, gallium, beryllium and silver.

Modern life will be almost unthinkable without transistors. They are the ubiquitous building blocks of all electronic devices: each computer chip contains billions of them. However, as the chips become smaller and smaller, the current 3D field-electronic transistors (FETs) are reaching their efficiency limit. A research team at the Center for Artificial Low Dimensional Electronic Systems, within the Institute for Basic Science (IBS), has developed the first 2D electronic circuit (FET) made of a single material. Published on Nature Nanotechnology, this study shows a new method to make metal and semiconductor from the same material in order to manifacture 2D FETs.

In simple terms, FETs can be thought as high-speed switches, comprised of two metal electrodes and a semiconducting channel in between. Electrons (or holes) move from the source electrode to the drain electrode, flowing through the channel. While 3D FETs have been scaled down to nanoscale dimensions successfully, their physical limitations are starting to emerge. Short semiconductor channel lengths lead to a decrease in performance: some electrons (or holes) are able to flow between the electrodes even when they should not, causing heat and efficiency reduction. To overcome this performance degradation, transistor channels have to be made with nanometer-scale thin materials. However, even thin 3D materials are not good enough, as unpaired electrons, part of the so-called “dangling bonds” at the surface interfere with the flowing electrons, leading to scattering.

Passing from thin 3D FETs to 2D FETs can overcome these problems and bring in new attractive properties. “FETs made from 2D semiconductors are free from short-channel effects because all electrons are confined in naturally atomically thin channels, free of dangling bonds at the surface,” explains Ji Ho Sung, first author of the study. Moreover, single- and few-layer form of layered 2D materials have a wide range of electrical and tunable optical properties, atomic-scale thickness, mechanical flexibility and large bandgaps (1~2 eV).

The major issue for 2D FET transistors is the existence of a large contact resistance at the interface between the 2D semiconductor and any bulk metal. To address this, the team devised a new technique to produce 2D transistors with semiconductor and metal made of the same chemical compound, molybdenum telluride (MoTe2). It is a polymorphic material, meaning that it can be used both as metal and as semiconductor. Contact resistance at the interface between the semiconductor and metallic MoTe2 is shown to be very low. Barrier height was lowered by a factor of 7, from 150meV to 22meV.

IBS scientists used the chemical vapor deposition (CVD) technique to build high quality metallic or semiconducting MoTe2 crystals. The polymorphism is controlled by the temperature inside a hot-walled quartz-tube furnace filled with NaCl vapor: 710°C to obtain metal and 670°C for a semiconductor.

The scientists also manufactured larger scale structures using stripes of tungsten diselenide (WSe2) alternated with tungsten ditelluride (WTe2). They first created a thin layer of semiconducting WSe2 with chemical vapor deposition, then scraped out some stripes and grew metallic WTe2 on its place.

It is anticipated that in the future, it would be possible to realize an even smaller contact resistance, reaching the theoretical quantum limit, which is regarded as a major issue in the study of 2D materials, including graphene and other transition metal dichalcogenide materials.

Many seashells, minerals, and semiconductor nanomaterials are made up of smaller crystals, which are assembled together like the pieces of a puzzle. Now, researchers have measured the forces that cause the crystals to assemble, revealing an orchestra of competing factors that researchers might be able to control.

The work has a variety of implications in both discovery and applied science. In addition to providing insights into the formation of minerals and semiconductor nanomaterials, it might also help scientists understand soil as it expands and contracts through wetting and drying cycles. In the applied realm, researchers might use the principles to develop new materials with unique properties for energy needs.

The results, published in the Proceedings of the National Academy of Sciences in July, describe how the arrangement of the atoms in the crystals creates forces that pull them together and align them for docking. The study reveals how the attraction becomes stronger or weaker as water is heated or salt is added, both of which are common processes in the natural world.

The multinational team, led by chemists Dongsheng Li and Jaehun Chun from the Department of Energy’s Pacific Northwest National Laboratory, explored the attractive forces between two crystal particles made from mica. A flaky mineral that is commonly used in electrical insulation, this silicon-based mineral is well-studied and easy to work with because it chips off in flat pieces with nearly-perfect crystal surfaces.

Forces and faces

Crystallization often occurs through assembly of multi-faceted building blocks: some faces on these smaller crystals line up better with others, like Lego blocks do. Li and Chun have been studying a specific crystallization process called oriented attachment. Among other distinguishing characteristics, oriented attachment occurs when smaller subunits of fledgling crystals align their best matching faces before clicking together.

The process creates various nonlinear forms: nanowires with branches, lattices that look like complicated honeycombs, and tetrapods — tiny structures that look like four-armed toy jacks. The molecular forces that contribute to this self-assembly are not well understood.

Molecular forces that come into play can attract or repel the tiny crystal building blocks to or from each other. These include a variety of textbook forces such as van der Waals, hydrogen bonding, and electrostatic, among others.

To explore the forces, Li, Chun and colleagues milled flat faces on tiny slabs of mica and put them on a device that measures the attraction between two pieces. Then they measured the attraction while twisting the faces relative to each other. The experiment allowed the mica to be bathed in a liquid that includes different salts, letting them test real-world scenarios.

The difference in this work was the liquid setup. Similar experiments by other researchers have been done dry under vacuum; in this work, the liquid created conditions that better simulate how real crystals form in nature and in large industrial methods. The team performed some of these experiments at EMSL, the Environmental Molecular Sciences Laboratory, a DOE Office of Science User Facility at PNNL.

Twist and salt

One of the first things the team found was that the attraction between two pieces of mica rose and fell as the faces twisted relative to each other, like when trying to make a sandwich out of two flat refrigerator magnets (go on, try it). In fact, the attraction rose and fell every 60 degrees, corresponding with the internal architecture of the mineral, which is almost hexagonal like a honeycomb cell.

Although other researchers more than a decade ago had predicted this cyclical attraction would happen, this is the first time scientists had measured the forces. Knowing the strength of the forces is key to manipulating crystallization in a research or industrial setting.

But other things were abuzz in the mica face-off as well. Between the two surfaces, the liquid environment housed electrically charged ions from salts, normal elements found during crystallization in nature. The water and the ions formed a somewhat stable layer between the surfaces that partly kept them separated. And as they moved toward each other, the two mica surfaces paused there, balanced between molecular attraction and repulsion by water and ions.

The team also found they could manipulate the strength of that attraction by changing the type of ions, their concentration, and the temperature. Different types of ions and their concentrations changed electrostatic repulsion between the mica surfaces. The size of the ions and how many charges they carried also created more or less space within the meddling layer.

Lastly, higher temperatures increased the strength of the attraction, contrary to how temperature behaves in simpler, less complex scenarios. The researchers built a model of the competing forces that included van der Waals, electrostatic, and hydration forces.

In the future, the researchers say, the principles gleaned from this study can be applied to other materials, which would be calculated for the material of interest. For example, manipulating the attraction might allow researchers to custom-build crystals of desired sizes and shapes and with unique properties. Overall, the work provides insights into crystal growth through nanoparticle assembly in synthetic, biological, and geochemical environments.