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Simultaneous enhancements in photon absorption and charge transport of bismuth vanadate photoanodes for solar water splitting

机译:同时增强钒酸铋铋光阳极的光子吸收和电荷传输用于太阳能水分解

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摘要

n-Type bismuth vanadate has been identified as one of the most promising photoanodes for use in a water-splitting photoelectrochemical cell. The major limitation of BiVO4 is its relatively wide bandgap (∼2.5 eV), which fundamentally limits its solar-to-hydrogen conversion efficiency. Here we show that annealing nanoporous bismuth vanadate electrodes at 350 °C under nitrogen flow can result in nitrogen doping and generation of oxygen vacancies. This gentle nitrogen treatment not only effectively reduces the bandgap by ∼0.2 eV but also increases the majority carrier density and mobility, enhancing electron–hole separation. The effect of nitrogen incorporation and oxygen vacancies on the electronic band structure and charge transport of bismuth vanadate are systematically elucidated by ab initio calculations. Owing to simultaneous enhancements in photon absorption and charge transport, the applied bias photon-to-current efficiency of nitrogen-treated BiVO4 for solar water splitting exceeds 2%, a record for a single oxide photon absorber, to the best of our knowledge.
机译:n型钒酸铋已被确定为用于水分解光电化学电池中最有希望的光阳极之一。 BiVO4的主要局限在于其相对较宽的带隙(〜2.5 eV),从根本上限制了其太阳能到氢的转换效率。在这里,我们显示了在氮气流下在350 C下对纳米多孔钒酸铋电极进行退火可以导致氮掺杂和氧空位的产生。这种温和的氮处理不仅有效地将带隙减小了约0.2 eV,而且还提高了多数载流子的密度和迁移率,从而增强了电子-空穴的分离。从头算起就系统地阐明了氮掺入和氧空位对钒酸铋电子带结构和电荷输运的影响。由于同时增强了光子吸收和电荷传输,据我们所知,经氮处理的BiVO4应用于太阳能水分解的偏置光子-电流效率超过2%,这是单个氧化物光子吸收剂的记录。

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