MacLeod Bradley A, Steirer K Xerxes, Young James L, Koldemir Unsal, Sellinger Alan, Turner John A, Deutsch Todd G, Olson Dana C
§Department of Materials Science and Engineering, University of Colorado, Boulder, Colorado 80309, United States.
∥Department of Chemistry and Geochemistry, Colorado School of Mines, Golden, Colorado 80401, United States.
ACS Appl Mater Interfaces. 2015 Jun 3;7(21):11346-50. doi: 10.1021/acsami.5b01814. Epub 2015 May 21.
The p-type semiconductor GaInP2 has a nearly ideal bandgap (∼1.83 eV) for hydrogen fuel generation by photoelectrochemical water splitting but is unable to drive this reaction because of misalignment of the semiconductor band edges with the water redox half reactions. Here, we show that attachment of an appropriate conjugated phosphonic acid to the GaInP2 electrode surface improves the band edge alignment, closer to the desired overlap with the water redox potentials. We demonstrate that this surface modification approach is able to adjust the energetic position of the band edges by as much as 0.8 eV, showing that it may be possible to engineer the energetics at the semiconductor/electrolyte interface to allow for unbiased water splitting with a single photoelectrode having a bandgap of less than 2 eV.
p型半导体GaInP2具有近乎理想的带隙(约1.83电子伏特),适用于通过光电化学水分解来产生氢燃料,但由于半导体带边与水氧化还原半反应不匹配,无法驱动该反应。在此,我们表明,在GaInP2电极表面附着适当的共轭膦酸可改善带边对齐,使其更接近与水氧化还原电位的理想重叠。我们证明,这种表面修饰方法能够将带边的能量位置调整多达0.8电子伏特,表明有可能在半导体/电解质界面设计能量,以允许使用带隙小于2电子伏特的单个光电极进行无偏压水分解。