光催化
光降解
铋
材料科学
苯酚
降级(电信)
电场
激进的
化学工程
光化学
化学
催化作用
有机化学
电信
物理
量子力学
计算机科学
工程类
冶金
作者
Zhaohui Wu,Wenlu Li,Jingyi Xu,Jianfang Jing,Junshan Li,Jie Shen,Lu Yang,Wenhui Feng,Shiying Zhang,Yongfa Zhu
标识
DOI:10.1002/sstr.202200380
摘要
Although the internal electric field (IEF) of bismuth oxyiodide (BiOI) is acknowledged as a potent driving force for efficient charge separation, enhancing the intensity of IEF remains a challenge. Herein, highly crystalline BiOI nanosheets with I‐rich surface are employed to intensify IEF and direct the charge migration. In comparison to I‐poor BiOI nanosheets, which possess Bi−O layer termination and I‐defects, the I‐rich BiOI demonstrates 62.5‐fold improvement in IEF intensity to its well‐developed high crystalline structure, and its IEF direction is reversed by the surface I‐rich layers. This intensified IEF of I‐rich BiOI induces numerous holes (h + ) to migrate to the surface of primary exposed (001) facets and electrons (e − ) to the lateral facets efficiently, resulting in efficient charge separation spatially. Additionally, the surface accumulates h + and superoxide radicals and acts in synergy to enhance the photodegradation of phenol. The photocatalytic activity of the I‐rich BiOI is found to be approximately fivefold and threefold higher than that of I‐poor BiOI under full spectra and visible light, respectively. Herein, the manipulation of IEF through surface and bulk structure regulation of BiOI for efficient charge separation is discussed, expecting to rationally improve photocatalytic performances.
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