Kenneth Chau, an assistant professor in the School of Engineering at UBC’s Okanagan campus, is a key investigator among colleagues at the National Institute of Standards and Technology in Maryland. Their work — the development of a flat lens — is published in the May 23 issue of the journal Nature.

Nearly all lenses — whether in an eye, a camera, or a microscope — are presently curved, which limits the aperture, or amount of light that enters.

“The idea of a flat lens goes way back to the 1960s when a Russian physicist came up with the theory,” Chau says. “The challenge is that there are no naturally occurring materials to make that type of flat lens. Through trial and error, and years of research, we have come up with a fairly simple recipe for a spray-on material that can act as that flat lens.”

The research team has developed a substance that can be affixed to surfaces like a glass slide and turn them into flat lenses for ultraviolet light imaging of biological specimens.

“Curved lenses always have a limited aperture,” he explains. “With a flat lens, suddenly you can make lenses with an arbitrary aperture size — perhaps as big as a football field.”

While the spray-on, flat lens represents a significant advancement in technology, it is only an important first step, Chau says.

“This is the closest validation we have of the original flat lens theory,” he says. “The recipe, now that we’ve got it working, is simple and cost-effective. Our next step is to extrapolate this technique further, explore the effect to the fullest, and advance it as far as we can take it.”

The technology could change the way imaging devices like cameras and scanners are designed.

Reprinted from University of British Columbia, via EurekAlert!, a service of AAAS.

While hydrogen is ubiquitous in the environment, producing and collecting molecular hydrogen for transportation and industrial uses is expensive and complicated. Just as importantly, a byproduct of most current methods of producing hydrogen is carbon monoxide, which is toxic to humans and animals.

The Duke engineers, using a new catalytic approach, have shown in the laboratory that they can reduce carbon monoxide levels to nearly zero in the presence of hydrogen and the harmless byproducts of carbon dioxide and water. They also demonstrated that they could produce hydrogen by reforming fuel at much lower temperatures than conventional methods, which makes it a more practical option.

Catalysts are agents added to promote chemical reactions. In this case, the catalysts were nanoparticle combinations of gold and iron oxide (rust), but not in the traditional sense. Current methods depend on gold nanoparticles ability to drive the process as the sole catalyst, while the Duke researchers made both the iron oxide and the gold the focus of the catalytic process.

The study appears online in the May issue of the Journal of Catalysis.

“Our ultimate goal is to be able to produce hydrogen for use in fuel cells,” said Titilayo “Titi” Shodiya, a graduate student working in the laboratory of senior researcher Nico Hotz, assistant professor of mechanical engineering and materials science at Duke’s Pratt School of Engineering. “Everyone is interested in sustainable and non-polluting ways of producing useful energy without fossil fuels,” said Shodiya, the paper’s first author.

Fuel cells produce electricity through chemical reactions, most commonly involving hydrogen. Also, many industrial processes require hydrogen as a chemical reagent and vehicles are beginning to use hydrogen as a primary fuel source.

“We were able through our system to consistently produce hydrogen with less than 0.002 percent (20 parts per million) of carbon monoxide,” Shodiya said.

The Duke researchers achieved these levels by switching the recipe for the nanoparticles used as catalysts for the reactions to oxidize carbon monoxide in hydrogen-rich gases. Traditional methods of cleaning hydrogen, which are not nearly as efficient as this new approach, also involve gold-iron oxide nanoparticles as the catalyst, the researchers said.

“It had been assumed that the iron oxide nanoparticles were only ‘scaffolds’ holding the gold nanoparticles together, and that the gold was responsible for the chemical reactions,” Sodiya said. “However, we found that increasing the surface area of the iron oxide dramatically increased the catalytic activity of the gold.”

One of the newest approaches to producing renewable energy is the use of biomass-derived alcohol-based sources, such as methanol. When methanol is treated with steam, or reformed, it creates a hydrogen-rich mixture that can be used in fuel cells.

“The main problem with this approach is that it also produces carbon monoxide, which is not only toxic to life, but also quickly damages the catalyst on fuel cell membranes that are crucial to the functioning of a fuel cell,” Hotz said. “It doesn’t take much carbon monoxide to ruin these membranes.”

The researchers ran the reaction for more than 200 hours and found no reduction in the ability of the catalyst to reduce the amount of carbon monoxide in the hydrogen gas.

“The mechanism for this is not exactly understood yet. However, while current thinking is that the size of the gold particles is key, we believe the emphasis of further research should focus on iron oxide’s role in the process,” Shodiya said.

The Duke team’s research was supported by the California Energy Commission and the Oak Ridge Associated Universities. Duke postdoctoral associates Oliver Schmidt and Wen Peng were also part of the research team.

Reprinted from Duke University.

Graduate students Siyuan Xing and Jia Jiang developed a new textile microfluidic platform using hydrophilic (water-attracting) threads stitched into a highly water-repellent fabric. They were able to create patterns of threads that suck droplets of water from one side of the fabric, propel them along the threads and expel them from the other side.

“We intentionally did not use any fancy microfabrication techniques so it is compatible with the textile manufacturing process and very easy to scale up,” said Xing, lead graduate student on the project.

It’s not just that the threads conduct water through capillary action. The water-repellent properties of the surrounding fabric also help drive water down the channels. Unlike conventional fabrics, the water-pumping effect keeps working even when the water-conducting fibers are completely saturated, because of the sustaining pressure gradient generated by the surface tension of droplets.

The rest of the fabric stays completely dry and breathable. By adjusting the pattern of water-conducting fibers and how they are stitched on each side of the fabric, the researchers can control where sweat is collected and where it drains away on the outside.

Workout enthusiasts, athletes and clothing manufacturers are all interested in fabrics that remove sweat and let the skin breathe. Cotton fibers, for example, wick away sweat — but during heavy exercise, cotton can get soaked, making it clingy and uncomfortable.

A paper describing the research was published recently in the journal Lab on a Chip. The work was funded in part by the National Science Foundation.

Reprinted from University of California Davis (UCD).

“Similar to the chloroplasts in green plants that carry out photosynthesis, our artificial photosynthetic system is composed of two semiconductor light absorbers, an interfacial layer for charge transport, and spatially separated co-catalysts,” says Peidong Yang, a chemist with Berkeley Lab’s Materials Sciences Division, who led this research. “To facilitate solar water- splitting in our system, we synthesized tree-like nanowire heterostructures, consisting of silicon trunks and titanium oxide branches. Visually, arrays of these nanostructures very much resemble an artificial forest.”

Yang, who also holds appointments with the University of California Berkeley’s Chemistry Department and Department of Materials Science and Engineering, is the corresponding author of a paper describing this research in the journal NANO Letters. The paper is titled “A Fully Integrated Nanosystem of Semiconductor Nanowires for Direct Solar Water Splitting.” Co-authors are Chong Liu, Jinyao Tang, Hao Ming Chen and Bin Liu.

Solar technologies are the ideal solutions for carbon-neutral renewable energy — there’s enough energy in one hour’s worth of global sunlight to meet all human needs for a year. Artificial photosynthesis, in which solar energy is directly converted into chemical fuels, is regarded as one of the most promising of solar technologies. A major challenge for artificial photosynthesis is to produce hydrogen cheaply enough to compete with fossil fuels. Meeting this challenge requires an integrated system that can efficiently absorb sunlight and produce charge-carriers to drive separate water reduction and oxidation half-reactions.

“In natural photosynthesis the energy of absorbed sunlight produces energized charge-carriers that execute chemical reactions in separate regions of the chloroplast,” Yang says. “We’ve integrated our nanowire nanoscale heterostructure into a functional system that mimics the integration in chloroplasts and provides a conceptual blueprint for better solar-to-fuel conversion efficiencies in the future.”

When sunlight is absorbed by pigment molecules in a chloroplast, an energized electron is generated that moves from molecule to molecule through a transport chain until ultimately it drives the conversion of carbon dioxide into carbohydrate sugars. This electron transport chain is called a “Z-scheme” because the pattern of movement resembles the letter Z on its side. Yang and his colleagues also use a Z-scheme in their system only they deploy two Earth abundant and stable semiconductors — silicon and titanium oxide — loaded with co-catalysts and with an ohmic contact inserted between them. Silicon was used for the hydrogen-generating photocathode and titanium oxide for the oxygen-generating photoanode. The tree-like architecture was used to maximize the system’s performance. Like trees in a real forest, the dense arrays of artificial nanowire trees suppress sunlight reflection and provide more surface area for fuel producing reactions.

“Upon illumination photo-excited electron−hole pairs are generated in silicon and titanium oxide, which absorb different regions of the solar spectrum,” Yang says. “The photo-generated electrons in the silicon nanowires migrate to the surface and reduce protons to generate hydrogen while the photo-generated holes in the titanium oxide nanowires oxidize water to evolve oxygen molecules. The majority charge carriers from both semiconductors recombine at the ohmic contact, completing the relay of the Z-scheme, similar to that of natural photosynthesis.”

Under simulated sunlight, this integrated nanowire-based artificial photosynthesis system achieved a 0.12-percent solar-to-fuel conversion efficiency. Although comparable to some natural photosynthetic conversion efficiencies, this rate will have to be substantially improved for commercial use. However, the modular design of this system allows for newly discovered individual components to be readily incorporated to improve its performance. For example, Yang notes that the photocurrent output from the system’s silicon cathodes and titanium oxide anodes do not match, and that the lower photocurrent output from the anodes is limiting the system’s overall performance.

“We have some good ideas to develop stable photoanodes with better performance than titanium oxide,” Yang says. “We’re confident that we will be able to replace titanium oxide anodes in the near future and push the energy conversion efficiency up into single digit percentages.”

This research was supported by the DOE Office of Science.

Reprinted from DOE/Lawrence Berkeley National Laboratory.

With the hand of nature trained on a beaker of chemical fluid, the most delicate flower structures have been formed in a Harvard laboratory — and not at the scale of inches, but microns.

These minuscule sculptures, curved and delicate, don’t resemble the cubic or jagged forms normally associated with crystals, though that’s what they are. Rather, fields of carnations and marigolds seem to bloom from the surface of a submerged glass slide, assembling themselves a molecule at a time.

By simply manipulating chemical gradients in a beaker of fluid, Wim L. Noorduin, a postdoctoral fellow at the Harvard School of Engineering and Applied Sciences (SEAS) and lead author of a paper appearing on the cover of the May 17 issue of Science, has found that he can control the growth behavior of these crystals to create precisely tailored structures.

“For at least 200 years, people have been intrigued by how complex shapes could have evolved in nature. This work helps to demonstrate what’s possible just through environmental, chemical changes,” says Noorduin.

The precipitation of the crystals depends on a reaction of compounds that are diffusing through a liquid solution. The crystals grow toward or away from certain chemical gradients as the pH of the reaction shifts back and forth. The conditions of the reaction dictate whether the structure resembles broad, radiating leaves, a thin stem, or a rosette of petals.

It is not unusual for chemical gradients to influence growth in nature; for example, delicately curved marine shells form from calcium carbonate under water, and gradients of signaling molecules in a human embryo help set up the plan for the body. Similarly, Harvard biologist Howard Berg has shown that bacteria living in colonies can sense and react to plumes of chemicals from one another, which causes them to grow, as a colony, into intricate geometric patterns.

Replicating this type of effect in the laboratory was a matter of identifying a suitable chemical reaction and testing, again and again, how variables like the pH, temperature, and exposure to air might affect the nanoscale structures.

The project fits right in with the work of Joanna Aizenberg, an expert in biologically inspired materials science, biomineralization, and self-assembly, and principal investigator for this research.

Aizenberg is the Amy Smith Berylson Professor of Materials Science at Harvard SEAS, Professor of Chemistry and Chemical Biology in the Harvard Department of Chemistry and Chemical Biology, and a Core Faculty Member of the Wyss Institute for Biologically Inspired Engineering at Harvard.

Her recent work has included the invention of an extremely slippery material, inspired by the pitcher plant, and the discovery of how bacteria use their flagella to cling to the surfaces of medical implants.

“Our approach is to study biological systems, to think what they can do that we can’t, and then to use these approaches to optimize existing technologies or create new ones,” says Aizenberg. “Our vision really is to build as organisms do.”

To create the flower structures, Noorduin and his colleagues dissolve barium chloride (a salt) and sodium silicate (also known as waterglass) into a beaker of water. Carbon dioxide from air naturally dissolves in the water, setting off a reaction which precipitates barium carbonate crystals. As a byproduct, it also lowers the pH of the solution immediately surrounding the crystals, which then triggers a reaction with the dissolved waterglass. This second reaction adds a layer of silica to the growing structures, uses up the acid from the solution, and allows the formation of barium carbonate crystals to continue.

“You can really collaborate with the self-assembly process,” says Noorduin. “The precipitation happens spontaneously, but if you want to change something then you can just manipulate the conditions of the reaction and sculpt the forms while they’re growing.”

Increasing the concentration of carbon dioxide, for instance, helps to create ‘broad-leafed’ structures. Reversing the pH gradient at the right moment can create curved, ruffled structures.

Noorduin and his colleagues have grown the crystals on glass slides and metal blades; they’ve even grown a field of flowers in front of President Lincoln’s seat on a one-cent coin.

“When you look through the electron microscope, it really feels a bit like you’re diving in the ocean, seeing huge fields of coral and sponges,” describes Noorduin. “Sometimes I forget to take images because it’s so nice to explore.”

In addition to her roles at Harvard SEAS, the Department of Chemistry and Chemical Biology, and the Wyss Institute, Joanna Aizenberg is Director of the Kavli Institute for Bionano Science and Technology at Harvard and Director of the Science Program at the Radcliffe Institute for Advanced Study.

Coauthors included Alison Grinthal, a research scientist at Harvard SEAS, and L. Mahadevan, who is the Lola England de Valpine Professor of Applied Mathematics at SEAS, Professor of Organismic and Evolutionary Biology and of Physics, and a Core Faculty Member at the Wyss Institute.

The project was supported by National Science Foundation grants to the Harvard Materials Research Science and Engineering Center (DMR-0820484) and the Harvard Center for Nanoscale Systems (ECS-0335765); and by the Netherlands Organization for Scientific Research.

Reprinted from Harvard School of Engineering and Applied Sciences.