光电流
分解水
钒酸铋
配体(生物化学)
材料科学
半导体
密度泛函理论
化学物理
化学
光电子学
计算化学
光催化
生物化学
催化作用
受体
作者
Mi Gyoung Lee,Kyoungsuk Jin,Ki Chang Kwon,Woonbae Sohn,Hoonkee Park,Kyoung Soon Choi,Yoo Kyung Go,Hongmin Seo,Jung Sug Hong,Ki Tae Nam,Ho Won Jang
标识
DOI:10.1002/advs.201800727
摘要
The band edge positions of semiconductors determine functionality in solar water splitting. While ligand exchange is known to enable modification of the band structure, its crucial role in water splitting efficiency is not yet fully understood. Here, ligand-engineered manganese oxide cocatalyst nanoparticles (MnO NPs) on bismuth vanadate (BiVO4) anodes are first demonstrated, and a remarkably enhanced photocurrent density of 6.25 mA cm-2 is achieved. It is close to 85% of the theoretical photocurrent density (≈7.5 mA cm-2) of BiVO4. Improved photoactivity is closely related to the substantial shifts in band edge energies that originate from both the induced dipole at the ligand/MnO interface and the intrinsic dipole of the ligand. Combined spectroscopic analysis and electrochemical study reveal the clear relationship between the surface modification and the band edge positions for water oxidation. The proposed concept has considerable potential to explore new, efficient solar water splitting systems.
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