[Due to the increasing size of the archives, each topic page now contains only the prior 365 days of content. Access to older stories is now solely through the Monthly Archive pages or the site search function.]
JCAP hybrid photocathode material shows promising performance in conversion of solar energy to hydrogen
March 09, 2014
A new study by Berkeley Lab researchers at the Joint Center for Artificial Photosynthesis (JCAP) shows that nearly 90% of the electrons generated by a new hybrid photocathode material designed to store solar energy in hydrogen are being stored in the target hydrogen molecules (Faradaic efficiency).
Gary Moore, a chemist and principal investigator with Berkeley Lab’s Physical Biosciences Division, led an efficiency analysis study of the material he and his research group have developed for catalyzing the production of hydrogen fuel from sunlight. (Earlier post.) This material, a p-type (100) gallium phosphide (GaP) semiconductor functionalized with molecular hydrogen-producing cobaloxime catalysts via polymer grafting, has the potential to address one of the major challenges in the use of artificial photosynthesis to make renewable solar fuels.
Israeli company reports successful stage 1 testing of solar CO2-to-fuels technology
January 26, 2014
Israel-based NewCO2Fuels (NCF), a subsidiary of GreenEarth Energy Limited in Australia, reported completion of stage 1 testing of its proof-of-concept system for the conversion of CO2 into fuels using solar energy. NewCO2Fuels was founded in 2011 to commercialize a technology developed by Prof. Jacob Karni’s laboratory at the Weizmann Institute of Science.
In passing the Stage 1 testing, NCF demonstrated technology that successfully dissociates CO2 into CO and oxygen in a heating environment, simulating the industrial waste heat sources that will be used as one of two energy sources in the commercial product. Importantly, the company said, the dissociation rate of the system was increased by a factor of 200 and the cost was reduced by a factor of 34, relative to the original dissociation apparatus demonstrated in 2010 at the laboratories of the Weizmann Institute of Science in Israel.
NSF/DOE partnership to award up to $18M for H2 production via advanced solar water-splitting technologies; separate DOE solicitation
November 14, 2013
A National Science Foundation and US Department of Energy (DOE) partnership on hydrogen production via solar water-splitting will award (NSF 14-511) up to $18 million to support the discovery and development of advanced materials systems and chemical processes for direct photochemical and/or thermochemical water splitting for application in the solar production of hydrogen fuel.
NSF and DOE are jointly funding this program solicitation issued by the NSF Chemical, Bioengineeering, Environmental and Transport Systems (CBET) Division; NSF expects to make 3 to 5 awards, each of up to 3-years duration. The DOE Fuel Cell Technologies Office also issued a separate solicitation for work a broader range of hydrogen production technologies. (DE-FOA-0000826)
Duke team develops new core-shell copper nanowire catalyst for efficient water oxidation for solar fuels
October 25, 2013
|A transparent film of copper nanowires was transformed into an electrocatalyst for water oxidation by electrodeposition of Ni or Co onto the surface of the nanowires. Chen et al. Click to enlarge.|
A team led by Benjamin J. Wiley at Duke University has introduced a new electrocatalyst for water oxidation consisting of a conductive network of core-shell nanowires that is just as efficient as conventional metal oxide films on indium tin oxide (ITO) and a great deal more transparent and robust. A paper on their work is published in the journal Angewandte Chemie.
Water oxidation (2H2O → O2 + 4e- + 4H+) is a key step for converting solar energy into chemical fuels. Nickel and cobalt oxides are attractive anode materials for the oxidation of water because they are readily available and demonstrate high catalytic activity. For use in photoelectric synthesis cells, in which chemical conversions are driven by light, the oxides are typically electrodeposited onto ITO substrates. ITO is used because of its high transmittance and low sheet resistance.