光催化
材料科学
极化(电化学)
可见光谱
晶体结构
极地的
电场
载流子
光电子学
化学工程
光化学
化学
催化作用
物理化学
结晶学
有机化学
物理
量子力学
天文
工程类
作者
Yan Chen,Weiyi Yang,Shuang Gao,Linggang Zhu,Caixia Sun,Qi Li
出处
期刊:Chemsuschem
[Wiley]
日期:2018-03-06
卷期号:11 (9): 1521-1532
被引量:61
标识
DOI:10.1002/cssc.201800180
摘要
A built-in electric field from polarization inside polar photocatalysts could provide the driving force for photogenerated electrons and holes to move in opposite directions for better separation to improve their photocatalytic performance. The photocatalytic performance of a polar photocatalyst of Bi2 MoO6 has been enhanced through the precise control of its structure to increase internal polarization. DFT calculations predicted that a shortened crystal lattice parameter b in Bi2 MoO6 could induce larger internal polarization, which was achieved by the modulation of the pH of the reaction solution during a solvothermal synthetic process. A series of Bi2 MoO6 samples were created with reaction solutions of pH≈1, 4, and 8; the crystal lattice parameter b was found to decrease gradually with increasing solution pH. Accordingly, these Bi2 MoO6 samples demonstrated a gradually enhanced photocatalytic performance with decreasing crystal lattice parameter b, as demonstrated by the photocatalytic degradation of sulfamethoxazole/phenol and disinfection of Staphylococcus aureus bacteria under visible-light illumination due to improved photogenerated charge-carrier separation. This study demonstrates an innovative design strategy for materials to further enhance the photocatalytic performance of polar photocatalysts for a broad range of technical applications.
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