光催化
分解水
可见光谱
光化学
材料科学
吸收(声学)
光子
电荷(物理)
载流子
电子转移
波长
激发
光谱学
光电子学
光子能量
吸收光谱法
析氧
电子
超快激光光谱学
光催化分解水
光诱导电子转移
半导体
化学
分子物理学
原子物理学
化学物理
氧气
电子空穴
表面光电压
光强度
作者
Kota Enomoto,Ryo Toyoshima,Zi Wang,Masaaki Yoshida,Kazuhiko Mase,Hiroshi Kondoh
标识
DOI:10.1021/acs.jpcc.5c05176
摘要
A crucial process in photocatalytic water splitting (PWS) is photoinduced charge transfer to reaction sites. Employing surface-sensitive in situ soft X-ray absorption spectroscopy, we measured the chemical-state evolution in Co under working conditions to track the electron and hole transfer to the CoOOH cocatalyst, which works as the oxygen evolution reaction site in Rh/Cr2O3–CoOOH/SrTiO3:Rh,Sb photocatalyst system. We found that the type of charge carrier transferred to the CoOOH cocatalyst is switched by the excitation-light energy; holes for UV light and electrons for visible light. Remarkably, the photocatalytic activity disappears under visible light irradiation, although the visible light photons are readily absorbed by the photocatalyst. We propose a possible scheme of charge transfer and consumption processes that is likely related to the PWS activity. This study highlights the pivotal role of excitation-light energy in charge transfer during the PWS.
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