光电流
光电阴极
材料科学
兴奋剂
分解水
钴
金属
制作
化学工程
无机化学
光电子学
光催化
冶金
化学
催化作用
生物化学
电子
病理
工程类
替代医学
物理
医学
量子力学
作者
Carlos Giovani Oliveira Bruziquesi,Matheus C. P. Stolzemburg,Rafael R. de Souza,Mariandry Rodríguez,Maria Luiza M. Rocco,Pedro Emílio Amador Salomão,André E. Nogueira,Zoraya López-Cabaña,Márcio C. Pereira,Adilson C. Silva
标识
DOI:10.1016/j.ijhydene.2022.10.195
摘要
CuBi2O4 is an excellent photocathode candidate in water-splitting photoelectrochemical cells. However, its poor photoelectrochemical stability caused by the reduction of Cu2+ to Cu metal limits its use. Here, we show a strategy to decrease the reduction of Cu2+ to Cu using cobalt as a sacrificial metal. Co-doped CuBi2O4 films were prepared by spray pyrolysis using Co2+ salt as the precursor. Co2+ ions replace Cu2+ in the CuBi2O4 structure, and subsequent heat treatment at 500 °C leads to partial oxidation of Co2+ to Co3+. As the reduction potential of Co3+/Co2+ is higher than that of Cu2+/Cu, Cu2+ reduction can be minimized. Comparatively, about 72% of the photocurrent produced by the CuBi2O4 film is lost in the first few minutes of illumination. In the Co-doped CuBi2O4 film, the photocurrent drops by less than 7%. Thus, the Co-doping can increase the CuBi2O4 photostability and be helpful for the fabrication of more stable photocathodes.
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