Category Archives: electronics

NEC and its ‘carbon nanobrush’

Long associated with the discovery of carbon nanotubes (CNTs), NEC Corporation has announced another carbon material, carbon nanobrushes, in a July 7, 2016 news item on,

NEC Corporation today [June 30, 2016] announced the discovery of a new nano carbon material, the “carbon nanobrush,” a fibrous aggregate of single-walled carbon nanohorns. Moreover, NEC has become the first company in the world to manufacture the carbon nanobrush.

A June 30, 2016 NEC Corporation press release, which originated the news item, provides more detail (Note: This excerpt has been reformatted for clarity),

“The ‘carbon nanobrush’ is a new nano carbon material that, like existing carbon nanohorns, has high water and solvent dispersity, and high adsorptivity, including substance adsorption, but has more than 10 times the electrical conductivity than existing carbon nanohorns, an important characteristic for industrial applications,” said Dr. Sumio Iijima, Senior Research Fellow, NEC Corporation. “With these characteristics, it is anticipated that the carbon nanobrush will help to improve the basic functionality of a range of devices, including increasing the speed of sensor and actuator responses, improving the output properties of batteries and capacitors, while increasing the electrical conductivity of rubber and plastic composite materials, as well as having application in a wide range of industries.”

1. TEM images of the obtained samples

2. Tips of single-walled carbon nanohorn

3. Spherical-carbon nanohorn aggregates

Carbon nanohorns are horn-shaped (figure 2) nano carbon structures 2-5 nanometers (nm) in diameter and 40-50nm in length, which until now have been produced as radial spherical aggregates (figure 3). The newly discovered carbon nanobrush is a uniquely shaped material. It is fibrous aggregates composed of radially-assembled graphene-based single-walled nanotubules, named here as fibrous aggregates of single-walled carbon nanohorns, whose structure resembles that of a round brush (figure 1).

Features of the “carbon nanobrush” include the following:

    1. Structure
      (1)Single-walled carbon nanohorns of 2-5nm in diameter and 40-50nm in length radially gather and are connected fibrously in several micrometers.
      (2)The single-walled carbon nanohorn which is a horn-shaped nano carbon structure with a large surface area radially gather and are connected fibrously in several micrometers. So it has a large surface area per unit mass (up to 1700㎡/g).
    1. Characteristics
      Like carbon nanohorns, the carbon nanobrush has high dispersibility, dispersing in water and organic solvents, for example. This means that it can be easily mixed with a variety of materials, making it easy to improve its characteristics as a base material.(2)Adsorptivity
      Like spherical carbon nanohorns, the carbon nanobrush can contain various substances in the nano-sized spaces inside the tubular structure, so it can be utilized as a high-performance adsorbent. When holes are formed on the surface of the carbon nanohorns by oxidation treatments, the inner space can be used, expanding the surface area by a factor of approximately five and greatly increasing adsorptivity.

      (3)Electrical conductivity
      As carbon nanobrush is a fibrous aggregate of radially-assembled carbon nanohorns, it has more than 10 times the electrical conductivity compared with existing spherical carbon nanohorn aggregates. As a result, they are highly effective in increasing the speed of sensor and actuator responses, increasing output properties of batteries and capacitors, and increasing the electrical conductivity of rubber and plastic composite materials.

  1. Production process
    Carbon nanobrush can be produced at room temperature and under atmospheric pressure using the laser ablation method where an iron-containing carbon target (mass of carbon) is irradiated by a laser with high power density. The simple production process means that they can be produced efficiently and at a low cost when compared to the cost of other nano carbon materials.

This technology was developed in part through collaborative research with the National Institute of Advanced Industrial Science and Technology (AIST).

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

Preparation and Characterization of Newly Discovered Fibrous Aggregates of Single-Walled Carbon Nanohorns by Ryota Yuge, Fumiyuki Nihey, Kiyohiko Toyama, and Masako Yudasaka. Advanced Materials DOI: 10.1002/adma.201602022 Version of Record online: 25 MAY 2016

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

This paper is behind a paywall.

For anyone interested in a history of carbon nanotubes, there’s my June 10, 2016 posting: The birth of carbon nanotubes (CNTs): a history, which includes a mention of NEC and its position as the discoverer of carbon nanotubes.

Memory material with functions resembling synapses and neurons in the brain

This work comes from the University of Twente’s MESA+ Institute for Nanotechnology according to a July 8, 2016 news item on ScienceDaily,

Our brain does not work like a typical computer memory storing just ones and zeroes: thanks to a much larger variation in memory states, it can calculate faster consuming less energy. Scientists of the MESA+ Institute for Nanotechnology of the University of Twente (The Netherlands) now developed a ferro-electric material with a memory function resembling synapses and neurons in the brain, resulting in a multistate memory. …

A July 8, 2016 University of Twente press release, which originated the news item, provides more technical detail,

The material that could be the basic building block for ‘brain-inspired computing’ is lead-zirconium-titanate (PZT): a sandwich of materials with several attractive properties. One of them is that it is ferro-electric: you can switch it to a desired state, this state remains stable after the electric field is gone. This is called polarization: it leads to a fast memory function that is non-volatile. Combined with processor chips, a computer could be designed that starts much faster, for example. The UT scientists now added a thin layer of zinc oxide to the PZT, 25 nanometer thickness. They discovered that switching from one state to another not only happens from ‘zero’ to ‘one’ vice versa. It is possible to control smaller areas within the crystal: will they be polarized (‘flip’) or not?

In a PZT layer without zinc oxide (ZnO) there are basically two memorystates. Adding a nano layer of ZnO, every state in between is possible as well.


By using variable writing times in those smaller areas, the result is that many states can be stored anywhere between zero and one. This resembles the way synapses and neurons ‘weigh’ signals in our brain. Multistate memories, coupled to transistors, could drastically improve the speed of pattern recognition, for example: our brain performs this kind of tasks consuming only a fraction of the energy a computer system needs. Looking at the graphs, the writing times seem quite long compared to nowaday’s processor speeds, but it is possible to create many memories in parallel. The function of the brain has already been mimicked in software like neurale networks, but in that case conventional digital hardware is still a limitation. The new material is a first step towards electronic hardware with a brain-like memory. Finding solutions for combining PZT with semiconductors, or even developing new kinds of semiconductors for this, is one of the next steps.

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

Multistability in Bistable Ferroelectric Materials toward Adaptive Applications by Anirban Ghosh, Gertjan Koster, and Guus Rijnders. Advanced Functional Materials DOI: 10.1002/adfm.201601353 Version of Record online: 4 JUL 2016

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

This paper is behind a paywall.

Unleashing graphene electronics potential with a trio of 2D nanomaterials

Graphene has excited a great deal of interest, especially with regard to its application in the field of electronics. However, it seems that graphene may need a little help from its friends, tantalum sulfide and boron nitride, according to a July 6, 2016 news item on ScienceDaily,

Graphene has emerged as one of the most promising two-dimensional crystals, but the future of electronics may include two other nanomaterials, according to a new study by researchers at the University of California, Riverside and the University of Georgia.

In research published Monday (July 4 [2016]) in the journal Nature Nanotechnology, the researchers described the integration of three very different two-dimensional (2D) materials to yield a simple, compact, and fast voltage-controlled oscillator (VCO) device. A VCO is an electronic oscillator whose oscillation frequency is controlled by a voltage input.

Titled “An integrated Tantalum Sulfide–Boron Nitride–Graphene Oscillator: A Charge-Density-Wave Device Operating at Room Temperature,” the paper describes the development of the first useful device that exploits the potential of charge-density waves to modulate an electrical current through a 2D material. The new technology could become an ultralow power alternative to conventional silicon-based devices, which are used in thousands of applications from computers to clocks to radios. The thin, flexible nature of the device would make it ideal for use in wearable technologies.

A July 5, 2016 University of California at Riverside (UCR) news release (also on EurekAlert) by Sarah Nightingale, which originated the news item, expands on the theme,

Graphene, a single layer of carbon atoms that exhibits exceptional electrical and thermal conductivities, shows promise as a successor to silicon-based transistors. However, its application has been limited by its inability to function as a semiconductor, which is critical for the ‘on-off’ switching operations performed by electronic components.

To overcome this shortfall, the researchers turned to another 2D nanomaterial, Tantalum Sulfide (TaS2). They showed that voltage-induced changes in the atomic structure of the ‘1T prototype’ of TaS2 enable it to function as an electrical switch at room temperature–a requirement for practical applications.

“There are many charge-density wave materials that have interesting electrical switching properties. However, most of them reveal these properties at very low temperature only. The particular polytype of TaS2 that we used can have abrupt changes in resistance above room temperature. That made a crucial difference,” said Alexander Balandin, UC presidential chair professor of electrical and computer engineering in UCR’s Bourns College of Engineering, who led the research team.

To protect the TaS2 from environmental damage, the researchers coated it with another 2D material, hexagonal boron nitrate, to prevent oxidation. By pairing the boron nitride-capped TaS2 with graphene, the team constructed a three-layer VCO that could pave the way for post-silicon electronics. In the proposed design, graphene functions as an integrated tunable load resistor, which enables precise voltage control of the current and VCO frequency. The prototype UCR devices operated at MHz frequency used in radios, and the extremely fast physical processes that define the device functionality allow for the operation frequency to increase all the way to THz.

Balandin said the integrated system is the first example of a functional voltage-controlled oscillator device comprising 2D materials that operates at room temperature.

“It is difficult to compete with silicon, which has been used and improved for the past 50 years. However, we believe our device shows a unique integration of three very different 2D materials, which utilizes the intrinsic properties of each of these materials. The device can potentially become a low-power alternative to conventional silicon technologies in many different applications,” Balandin said.

The electronic function of graphene envisioned in the proposed 2D device overcomes the problem associated with the absence of the energy band gap, which so far prevented graphene’s use as the transistor channel material. The extremely high thermal conductivity of graphene comes as an additional benefit in the device structure, by facilitating heat removal. The unique heat conduction properties of graphene were experimentally discovered and theoretically explained in 2008 by Balandin’s group at UCR. The Materials Research Society recognized this groundbreaking achievement by awarding Balandin the MRS Medal in 2013.

The Balandin group also demonstrated the first integrated graphene heat spreaders for high-power transistors and light-emitting diodes. “In those applications, graphene was used exclusively as heat conducting material. Its thermal conductivity was the main property. In the present device, we utilize both electrical and thermal conductivity of graphene,” Balandin added.

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

A charge-density-wave oscillator based on an integrated tantalum disulfide–boron nitride–graphene device operating at room temperature by Guanxiong Liu, Bishwajit Debnath, Timothy R. Pope, Tina T. Salguero, Roger K. Lake, & Alexander A. Balandin. Nature Nanotechnology (2016) doi:10.1038/nnano.2016.108 Published online 04 July 2016

This paper is behind a paywall.

Artificial synapse rivals biological synapse in energy consumption

How can we make computers be like biological brains which do so much work and use so little power? It’s a question scientists from many countries are trying to answer and it seems South Korean scientists are proposing an answer. From a June 20, 2016 news item on Nanowerk,

News) Creation of an artificial intelligence system that fully emulates the functions of a human brain has long been a dream of scientists. A brain has many superior functions as compared with super computers, even though it has light weight, small volume, and consumes extremely low energy. This is required to construct an artificial neural network, in which a huge amount (1014)) of synapses is needed.

Most recently, great efforts have been made to realize synaptic functions in single electronic devices, such as using resistive random access memory (RRAM), phase change memory (PCM), conductive bridges, and synaptic transistors. Artificial synapses based on highly aligned nanostructures are still desired for the construction of a highly-integrated artificial neural network.

Prof. Tae-Woo Lee, research professor Wentao Xu, and Dr. Sung-Yong Min with the Dept. of Materials Science and Engineering at POSTECH [Pohang University of Science & Technology, South Korea] have succeeded in fabricating an organic nanofiber (ONF) electronic device that emulates not only the important working principles and energy consumption of biological synapses but also the morphology. …

A June 20, 2016 Pohang University of Science & Technology (POSTECH) news release on EurekAlert, which originated the news item, describes the work in more detail,

The morphology of ONFs is very similar to that of nerve fibers, which form crisscrossing grids to enable the high memory density of a human brain. Especially, based on the e-Nanowire printing technique, highly-aligned ONFs can be massively produced with precise control over alignment and dimension. This morphology potentially enables the future construction of high-density memory of a neuromorphic system.

Important working principles of a biological synapse have been emulated, such as paired-pulse facilitation (PPF), short-term plasticity (STP), long-term plasticity (LTP), spike-timing dependent plasticity (STDP), and spike-rate dependent plasticity (SRDP). Most amazingly, energy consumption of the device can be reduced to a femtojoule level per synaptic event, which is a value magnitudes lower than previous reports. It rivals that of a biological synapse. In addition, the organic artificial synapse devices not only provide a new research direction in neuromorphic electronics but even open a new era of organic electronics.

This technology will lead to the leap of brain-inspired electronics in both memory density and energy consumption aspects. The artificial synapse developed by Prof. Lee’s research team will provide important potential applications to neuromorphic computing systems and artificial intelligence systems for autonomous cars (or self-driving cars), analysis of big data, cognitive systems, robot control, medical diagnosis, stock trading analysis, remote sensing, and other smart human-interactive systems and machines in the future.

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

Organic core-sheath nanowire artificial synapses with femtojoule energy consumption by Wentao Xu, Sung-Yong Min, Hyunsang Hwang, and Tae-Woo Lee. Science Advances  17 Jun 2016: Vol. 2, no. 6, e1501326 DOI: 10.1126/sciadv.1501326

This paper is open access.

Carrying a solar cell on a pencil or glass slide?

Caption: Ultra-thin solar cells are flexible enough to bend around small objects, such as the 1mm-thick edge of a glass slide, as shown here. Credit: Juho Kim, et al/ APL

Caption: Ultra-thin solar cells are flexible enough to bend around small objects, such as the 1mm-thick edge of a glass slide, as shown here. Credit: Juho Kim, et al/ APL

Yes, this is another wearable electronics story and this time, it’s from South Korea. A June 20, 2016 news item on ScienceDaily announces remarkably thin and flexible photovoltaics,

Scientists in South Korea have made ultra-thin photovoltaics flexible enough to wrap around the average pencil. The bendy solar cells could power wearable electronics like fitness trackers and smart glasses. …

A June 20, 2016 American Institute of Physics news release on EurekAlert, which originated the news item, expands on the theme,

Thin materials flex more easily than thick ones – think a piece of paper versus a cardboard shipping box. The reason for the difference: The stress in a material while it’s being bent increases farther out from the central plane. Because thick sheets have more material farther out they are harder to bend.

“Our photovoltaic is about 1 micrometer thick,” said Jongho Lee, an engineer at the Gwangju Institute of Science and Technology in South Korea. One micrometer is much thinner than an average human hair. Standard photovoltaics are usually hundreds of times thicker, and even most other thin photovoltaics are 2 to 4 times thicker.

The researchers made the ultra-thin solar cells from the semiconductor gallium arsenide. They stamped the cells directly onto a flexible substrate without using an adhesive that would add to the material’s thickness. The cells were then “cold welded” to the electrode on the substrate by applying pressure at 170 degrees Celcius and melting a top layer of material called photoresist that acted as a temporary adhesive. The photoresist was later peeled away, leaving the direct metal to metal bond.

The metal bottom layer also served as a reflector to direct stray photons back to the solar cells. The researchers tested the efficiency of the device at converting sunlight to electricity and found that it was comparable to similar thicker photovoltaics. They performed bending tests and found the cells could wrap around a radius as small as 1.4 millimeters.

The team also performed numerical analysis of the cells, finding that they experience one-fourth the amount of strain of similar cells that are 3.5 micrometers thick.

“The thinner cells are less fragile under bending, but perform similarly or even slightly better,” Lee said.

A few other groups have reported solar cells with thicknesses of around 1 micrometer, but have produced the cells in different ways, for example by removing the whole substract by etching.

By transfer printing instead of etching, the new method developed by Lee and his colleagues may be used to make very flexible photovoltaics with a smaller amount of materials.

The thin cells can be integrated onto glasses frames or fabric and might power the next wave of wearable electronics, Lee said.

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

Ultra-thin flexible GaAs photovoltaics in vertical forms printed on metal surfaces without interlayer adhesives by Juho Kim, Jeongwoo Hwang, Kwangsun Song, Namyun Kim, Jae Cheol Shin, and Jongho Lee. Appl. Phys. Lett. 108, 253101 (2016);

This paper is open access.

Turning gold into see-through rubber for an updated Rumpelstiltskin story

Rumpelstiltskin is a fairy tale whereby a young girl is trapped by her father’s lie that she can spin straw into gold. She is forced to spin gold by the King under pain of execution when an imp offers to help in exchange for various goods. As she succeeds each time, the King demands more until finally she has nothing left to trade for the imp’s help. Well, there is one last thing: her first-born child. She agrees to the bargain and she marries the King. On the birth of their first child, the imp reappears and under pressure of her pleas makes one last bargain. She must guess his name which she does, Rumplestiltskin. (The full story along with variants is here in this Wikipedia entry.)

With this latest research, we have a reverse Rumpelstiltskin story where gold is turned into something else according to a June 13, 2016 news item on Nanowerk (Note: A link has been removed),

Flexible solar panels that could be rolled up for easy transport and other devices would benefit from transparent metal electrodes that can conduct electricity, are stretchable, and resist damage following repeated stretching. Researchers found that topology and the adhesion between a metal nanomesh and the underlying substrate played key roles in creating such materials. The metal nanomesh can be stretched to three times its length while maintaining a transparency comparable to similar commercial materials used in solar cells and flat panel displays. Also, nanomeshes on pre-stretched slippery substrates led to electrodes that didn’t wear out, even after being stretched 50,000 times (Proceedings of the National Academy of Sciences, “Fatigue-free, superstretchable, transparent, and biocompatible metal electrodes”).

Tuning topology and adhesion of metal nanomeshes has led to super stretchable, transparent electrodes that don’t wear out. The scanning electron microscopy image shows the structure of a gold mesh created with a special lithographic technique that controlled the dimensions of the mesh structure. Optimizing this structure and its adhesion to the substrate was key to achieving super stretchability and long lifetimes in use—nanomeshes on pre-stretched slippery substrates did not show signs of wear even after repeated stretching, up to 50,000 cycles.

Tuning topology and adhesion of metal nanomeshes has led to super stretchable, transparent electrodes that don’t wear out. The scanning electron microscopy image shows the structure of a gold mesh created with a special lithographic technique that controlled the dimensions of the mesh structure. Optimizing this structure and its adhesion to the substrate was key to achieving super stretchability and long lifetimes in use—nanomeshes on pre-stretched slippery substrates did not show signs of wear even after repeated stretching, up to 50,000 cycles.

A June 9, 2016 US Dept. of Energy news release,which originated the news item, provides more detail,

Next-generation flexible electronics require highly stretchable and transparent electrodes. Fatigue, structural damage due to repeated use, is deadly in metals as it leads to poor conductivity and it commonly occurs in metals with repeated stretching—even with short elongations. However, few electronic conductors are transparent and stretchable, even fewer can be cyclically stretched to a large strain without causing fatigue. Now researchers led by the University of Houston found that optimizing topology of a metal nanomesh and its adhesion to an underlying substrate improved stretchability and eliminated fatigue, while maintaining transparency. A special lithographic technique called “grain boundary lithography” controlled the dimensions of the mesh structure. The metal nanomesh remained transparent after being stretched to three times its length. Gold nanomeshes on prestretched slippery substrates impressively showed no wear when stretched 50,000 times. The slippery surface advantageously allowed the structure of the nanomesh to reorient to relax the stress. Such electrically conductive, flexible, and transparent electrodes could lead to next-generation flexible electronics such as advanced solar cells.  The nanomesh electrodes are also promising for implantable electronics because the nanomeshes are biocompatible.

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

Fatigue-free, superstretchable, transparent, and biocompatible metal electrodes by Chuan Fei Guo, Qihan Liu, Guohui Wang, Yecheng Wang, Zhengzheng Shi, Zhigang Suo, Ching-Wu Chu, and Zhifeng Ren. Proceedings of the National Academy of Sciences, vol. 112 no. 40,  12332–12337, doi: 10.1073/pnas.1516873112

This paper appears to be open access.

A new, stable open-shell carbon molecule from Oregon

This discovery could one day make organic solar cells more efficient than silicon ones. Researchers at the University of Oregon announced their discovery in a June 9, 2016 news item on ScienceDaily,

University of Oregon chemists have synthesized a stable and long-lasting carbon-based molecule that, they say, potentially could be applicable in solar cells and electronic devices.

The molecule changes its bonding patterns to a magnetic biradical state when heated; it then returns to a fully bonded non-magnetic closed state at room temperature. That transition, they report, can be done repeatedly without decomposition. It remains stable in the presence of both heat and oxygen.

A June 9, 2016 University of Oregon news release on EurekAlert, which originated the news item, provides more detail,


Biradical refers to organic compounds, known as open-shell molecules, that have two free-flowing, non-bonding electrons. Producing them using techniques to control their electron spin, and thus provide semiconducting properties, in a heated state has been hampered by instability since the first synthetic biradical hydrocarbon was made in 1907.

“Potentially our approach could help to make organic solar cells more efficient than silicon solar cells, but that’s probably far in the future,” said UO doctoral student Gabriel E. Rudebusch, the paper’s lead author. “Our synthesis is rapid and efficient. We easily can make a gram of this compound, which is very stable when exposed to oxygen and heat. This stability has been almost unheard of in the literature about biradical compounds.”

The four-step synthesis of the compound — diindenoanthracene, or DIAn — and how it held up when tested in superconducting materials were detailed in a proof-of-principle paper published online May 23 by the journal Nature Chemistry. The UO team collaborated with experts in Japan, Spain and Sweden.

The molecular framework for the new molecule involves the hydrocarbon anthracene, which has three linearly fused hexagonal benzene rings, in combination with two five-membered pentagonal rings.

“The big difference between our new molecule and a lot of other biradical molecules that have been produced is those five-membered rings,” said co-author Michael M. Haley, who holds the UO’s Richard M. and Patricia H. Noyes Professorship in Chemistry. “They have the inherent ability to accept electrons or give up electrons. This means DIAn can move both negative and positive charges, which is an essential property for useful devices such as transistors and solar cells. Also, we can heat up our molecule to 150 degrees Celsius, bring it back to room temperature and heat it up again, repeatedly, and we see no decomposition in its reaction to oxygen. The unique features of DIAn are essential if these molecules are to have a use in the real world.”

Haley’s lab is now seeking to develop derivatives of the new molecule to help move the technology forward into potential applications.

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

Diindeno-fusion of an anthracene as a design strategy for stable organic biradicals by Gabriel E. Rudebusch, José L. Zafra, Kjell Jorner, Kotaro Fukuda, Jonathan L. Marshall, Iratxe Arrechea-Marcos, Guzmán L. Espejo, Rocío Ponce Ortiz, Carlos J. Gómez-García, Lev N. Zakharov, Masayoshi Nakano, Henrik Ottosson, Juan Casado & Michael M. Haley. Nature Chemistry (2016)  doi:10.1038/nchem.2518 Published online 23 May 2016

This paper is behind a paywall.

There is another June 9, 2016 University of Oregon news release by Jim Barlow about this discovery. It covers much of the same material but focuses more closely on Rudebusch’s perspective.

Diamond-based electronics?

A May 24, 2016 news item on ScienceDaily describes the latest research on using diamonds as semiconductors,

Along with being a “girl’s best friend,” diamonds also have remarkable properties that could make them ideal semiconductors. This is welcome news for electronics; semiconductors are needed to meet the rising demand for more efficient electronics that deliver and convert power.

The thirst for electronics is unlikely to cease and almost every appliance or device requires a suite of electronics that transfer, convert and control power. Now, researchers have taken an important step toward that technology with a new way to dope single crystals of diamonds, a crucial process for building electronic devices.

A May 24, 2016 American Institute of Physics (AIP) news release (also on EurekAlert), which originated the news item, provides more detail,

For power electronics, diamonds could serve as the perfect material. They are thermally conductive, which means diamond-based devices would dissipate heat quickly and easily, foregoing the need for bulky and expensive methods for cooling. Diamond can also handle high voltages and power. Electrical currents also flow through diamonds quickly, meaning the material would make for energy efficient devices.

But among the biggest challenges to making diamond-based devices is doping, a process in which other elements are integrated into the semiconductor to change its properties. Because of diamond’s rigid crystalline structure, doping is difficult.

Currently, you can dope diamond by coating the crystal with boron and heating it to 1450 degrees Celsius. But it’s difficult to remove the boron coating at the end. This method only works on diamonds consisting of multiple crystals stuck together. Because such polydiamonds have irregularities between the crystals, single-crystals would be superior semiconductors.

You can dope single crystals by injecting boron atoms while growing the crystals artificially. The problem is the process requires powerful microwaves that can degrade the quality of the crystal.

Now, Ma [Zhengqiang (Jack) Ma, an electrical and computer engineering professor at the University of Wisconsin-Madison] and his colleagues have found a way to dope single-crystal diamonds with boron at relatively low temperatures and without any degradation. The researchers discovered if you bond a single-crystal diamond with a piece of silicon doped with boron, and heat it to 800 degrees Celsius, which is low compared to the conventional techniques, the boron atoms will migrate from the silicon to the diamond. It turns out that the boron-doped silicon has defects such as vacancies, where an atom is missing in the lattice structure. Carbon atoms from the diamond will fill those vacancies, leaving empty spots for boron atoms.

This technique also allows for selective doping, which means more control when making devices. You can choose where to dope a single-crystal diamond simply by bonding the silicon to that spot.

The new method only works for P-type doping, where the semiconductor is doped with an element that provides positive charge carriers (in this case, the absence of electrons, called holes).

“We feel like we found a very easy, inexpensive, and effective way to do it,” Ma said. The researchers are already working on a simple device using P-type single-crystal diamond semiconductors.

But to make electronic devices like transistors, you need N-type doping that gives the semiconductor negative charge carriers (electrons). And other barriers remain. Diamond is expensive and single crystals are very small.

Still, Ma says, achieving P-type doping is an important step, and might inspire others to find solutions for the remaining challenges. Eventually, he said, single-crystal diamond could be useful everywhere — perfect, for instance, for delivering power through the grid.

Here’s an image the researchers have released,

Optical image of a diode array on a natural single crystalline diamond plate. (The image looks blurred due to light scattering by the array of small pads on top of the diamond plate.) Inset shows the deposited anode metal on top of heavy doped Si nanomembrane that is bonded to natural single crystalline diamond. CREDIT: Jung-Hun Seo

Optical image of a diode array on a natural single crystalline diamond plate. (The image looks blurred due to light scattering by the array of small pads on top of the diamond plate.) Inset shows the deposited anode metal on top of heavy doped Si nanomembrane that is bonded to natural single crystalline diamond. CREDIT: Jung-Hun Seo Courtesy: American Institute of Physics

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

Thermal diffusion boron doping of single-crystal natural diamond by Jung-Hun Seo, Henry Wu, Solomon Mikael, Hongyi Mi, James P. Blanchard, Giri Venkataramanan, Weidong Zhou, Shaoqin Gong, Dane Morgan, and Zhenqiang Ma. J. Appl. Phys. 119, 205703 (2016);

This paper appears to be open access.

Light-captured energetics (harvesting light for optoelectronics)

Comparing graphene to a tiger is unusual but that’s what researcher Sanfeng Wu does—eventually—in a May 13, 2016 University of Washington news release (also on EurekAlert) about his work,

In the quest to harvest light for electronics, the focal point is the moment when photons — light particles — encounter electrons, those negatively-charged subatomic particles that form the basis of our modern electronic lives. If conditions are right when electrons and photons meet, an exchange of energy can occur. Maximizing that transfer of energy is the key to making efficient light-captured energetics possible.

“This is the ideal, but finding high efficiency is very difficult,” said University of Washington physics doctoral student Sanfeng Wu. “Researchers have been looking for materials that will let them do this — one way is to make each absorbed photon transfer all of its energy to many electrons, instead of just one electron in traditional devices.”

In traditional light-harvesting methods, energy from one photon only excites one electron or none depending on the absorber’s energy gap, transferring just a small portion of light energy into electricity. The remaining energy is lost as heat. But in a paper released May 13 in Science Advances, Wu, UW associate professor Xiaodong Xu and colleagues at four other institutions describe one promising approach to coax photons into stimulating multiple electrons. Their method exploits some surprising quantum-level interactions to give one photon multiple potential electron partners. Wu and Xu, who has appointments in the UW’s Department of Materials Science & Engineering and the Department of Physics, made this surprising discovery using graphene.

There has been intense research on graphene’s electrical properties but the researchers’ discovery adds a new property to be investigated (from the news release),

“Graphene is a substance with many exciting properties,” said Wu, the paper’s lead author. “For our purposes, it shows a very efficient interaction with light.”

Graphene is a two-dimensional hexagonal lattice of carbon atoms bonded to one another, and electrons are able to move easily within graphene. The researchers took a single layer of graphene — just one sheet of carbon atoms thick — and sandwiched it between two thin layers of a material called boron-nitride.

Boron-nitride is a material that has excited a great deal of interest in the last 12 to 18 months (from the news release),

“Boron-nitride has a lattice structure that is very similar to graphene, but has very different chemical properties,” said Wu. “Electrons do not flow easily within boron-nitride; it essentially acts as an insulator.”

Xu and Wu discovered that when the graphene layer’s lattice is aligned with the layers of boron-nitride, a type of “superlattice” is created with properties allowing efficient optoelectronics that researchers had sought. These properties rely on quantum mechanics, the occasionally baffling rules that govern interactions between all known particles of matter. Wu and Xu detected unique quantum regions within the superlattice known as Van Hove singularities.

Here’s an animated .gif illustrating the superlattice in action,

The Moire superlattice they created by aligning graphene and boron-nitride. Credit: Sanfeng Wu.

The Moire superlattice they created by aligning graphene and boron-nitride. Credit: Sanfeng Wu.

The news release goes on to describe the Van Hove singularities within the superlattice and to mention the ‘tiger’,

“These are regions of huge electron density of states, and they were not accessed in either the graphene or boron-nitride alone,” said Wu. “We only created these high electron density regions in an accessible way when both layers were aligned together.”

When Xu and Wu directed energetic photons toward the superlattice, they discovered that those Van Hove singularities were sites where one energized photon could transfer its energy to multiple electrons that are subsequently collected by electrodes— not just one electron or none with the remaining energy lost as heat. By a conservative estimate, Xu and Wu report that within this superlattice one photon could “kick” as many as five electrons to flow as current.

With the discovery of collecting multiple electrons upon the absorption of one photon, researchers may be able to create highly efficient devices that could harvest light with a large energy profit. Future work would need to uncover how to organize the excited electrons into electrical current for optimizing the energy-converting efficiency and remove some of the more cumbersome properties of their superlattice, such as the need for a magnetic field. But they believe this efficient process between photons and electrons represents major progress.

“Graphene is a tiger with great potential for optoelectronics, but locked in a cage,” said Wu. “The singularities in this superlattice are a key to unlocking that cage and releasing graphene’s potential for light harvesting application.”

H/t to a May 13, 2016 news item on

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

Multiple hot-carrier collection in photo-excited graphene Moiré superlattices by Sanfeng Wu, Lei Wang, You Lai, Wen-Yu Shan, Grant Aivazian, Xian Zhang, Takashi Taniguchi, Kenji Watanabe, Di Xiao, Cory Dean, James Hone, Zhiqiang Li, and Xiaodong Xu. Science Advances 13 May 2016: Vol. 2, no. 5, e1600002 DOI: 10.1126/sciadv.1600002

This paper is open access.