Zhang Liwu, Lin Chia-Yu, Valev Ventsislav K, Reisner Erwin, Steiner Ullrich, Baumberg Jeremy J
Cavendish Laboratory, Department of Physics, University of Cambridge, Cambridge, CB3 0HE, UK.
Small. 2014 Oct 15;10(19):3970-8. doi: 10.1002/smll.201400970. Epub 2014 Jun 11.
Photo-electrochemical water splitting is a very promising and environmentally friendly route for the conversion of solar energy into hydrogen. However, the solar-to-H2 conversion efficiency is still very low due to rapid bulk recombination of charge carriers. Here, a photonic nano-architecture is developed to improve charge carrier generation and separation by manipulating and confining light absorption in a visible-light-active photoanode constructed from BiVO4 photonic crystal and plasmonic nanostructures. Synergistic effects of photonic crystal stop bands and plasmonic absorption are observed to operate in this photonic nanostructure. Within the scaffold of an inverse opal photonic crystal, the surface plasmon resonance is significantly enhanced by the photonic Bragg resonance. Nanophotonic photoanodes show AM 1.5 photocurrent densities of 3.1 ± 0.1 mA cm(-2) at 1.23 V versus RHE, which is among the highest for oxide-based photoanodes and over 4 times higher than the unstructured planar photoanode.
光电化学水分解是一种将太阳能转化为氢能的非常有前景且环保的途径。然而,由于电荷载流子在体内的快速复合,太阳能到氢能的转换效率仍然很低。在此,通过在由BiVO4光子晶体和等离子体纳米结构构建的可见光活性光阳极中操纵和限制光吸收,开发了一种光子纳米结构,以提高电荷载流子的产生和分离。观察到光子晶体禁带和等离子体吸收的协同效应在这种光子纳米结构中起作用。在反蛋白石光子晶体的支架内,表面等离子体共振通过光子布拉格共振得到显著增强。纳米光子光阳极在相对于可逆氢电极1.23 V时的AM 1.5光电流密度为3.1±0.1 mA cm(-2),这是基于氧化物的光阳极中最高的之一,比无结构的平面光阳极高出4倍以上。