Researchers combined 2 2D materials – black phosphorus and bismuth vanadate – to form a biologically inspired water-splitting catalyst. Normal sunlight could drive the reactions and careful design of the catalyst enabled the expected ratio of hydrogen and oxygen production. Burning hydrogen produces harmless water with the potential to eliminate CO2 emissions and their environmental burden. In pursuit of technologies that could lead to a breakthrough in achieving a hydrogen economy, a key issue is making hydrogen cheaply. Using catalysts to split water is the ideal way to generate hydrogen, but doing so usually requires an energy input from other chemicals, electricity, or a portion of sunlight which has high enough energy.
Now researchers at Osaka University have developed a new catalytic system for efficiently splitting water and making hydrogen with energy from normal sunlight. “It has not been possible to use visible light for photocatalysis, but our approach of combining nanostructured black phosphorus for water reduction to hydrogen and bismuth vanadate for water oxidation to oxygen lets us make use of a wide range of the solar spectrum to make hydrogen and oxygen with unprecedented efficiency,” lead author Mingshan Zhu says.
Black phosphorus has a flat, two-dimensional structure similar to that of graphene and strongly absorbs light across the whole of the visible spectrum. The researchers combined the black phosphorus with bismuth vanadate, which is a well-known water oxidation catalyst. The two components of this new catalyst could rapidly transfer electrons excited by sunlight. The amounts of the two components was also optimized in the catalyst, leading to production of hydrogen and oxygen gases in an ideal 2:1 ratio.
Coauthor Tetsuro Majima says, “The realization of hydrogen production powered by sunlight is the foundation of a hydrogen-oriented society. Our contribution overcomes a significant hurdle, but much work remains to be done to make hydrogen a practical fuel source in the future.” http://resou.osaka-u.ac.jp/en/research/2018/20180112_1
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