极化子
光电流
化学物理
氢
掺杂剂
兴奋剂
材料科学
密度泛函理论
电子
化学吸附
电导率
电子传输链
纳米孔
化学
光电子学
光化学
纳米技术
物理化学
吸附
物理
计算化学
有机化学
量子力学
生物化学
作者
Hao Wu,Lei Zhang,Songying Qu,Aijun Du,Junwang Tang,Yun Hau Ng
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-04-13
卷期号:8 (5): 2177-2184
被引量:25
标识
DOI:10.1021/acsenergylett.3c00465
摘要
Hydrogen dopants and oxygen vacancies (OVs) play crucial roles in BiVO4 photoanodes. However, the decisive factor determining the charge transport of the hydrogenated BiVO4, particularly with electron small polaron formation, remains elusive. Here we show a decreased charge transport barrier upon mildly hydrogenating the nanoporous BiVO4 photoanode, as evidenced by the thermally activating photocurrent responses. Monochromatic light photoelectrochemical performance, temperature-dependent conductivity, proton nuclear magnetic resonance, and density functional theory calculation disclose that the external hydrogen atoms occupy the intrinsic OVs in the BiVO4, reducing the hopping activation energy and facilitating electron small polaron transport. The resulting BiVO4 photoanode with NiFeOx cocatalyst achieves an applied-bias photon-to-current efficiency of 1.91% at 0.58 V vs RHE with front-illumination. This study extends the common understanding of the beneficial role in conventional donor density/surface chemisorption mediations of hydrogen doping to now include small polaron hopping.
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