异质结
材料科学
光催化
降级(电信)
电场
电子转移
电子
光电子学
化学工程
化学物理
光化学
计算机科学
催化作用
电信
化学
物理
工程类
量子力学
生物化学
作者
Shaoxuan Pang,Yilin Dong,Dongyu Xu,Qiuwen Wang,Weihong Gao,Lijun Zhang,Kang Wang,Guangming Zhang,Longyi Lv,Yuguo Xia,Zhijun Ren,Pengfei Wang
标识
DOI:10.1016/j.jmst.2023.02.039
摘要
Heterojunction photocatalysts have shown considerable activities for organic pollutants degradation. However, the faint connection interface and inferior charge shift efficiency critically block the property of heterojunction photocatalysis. Herein, Bi2O2S/NiFe2O4 nanosheets heterojunction with ultrastrong interface interaction and high internal electric field are designed by an in-situ growth method. Tentative and theoretical consequences prove that the interfacial interaction and internal electric field not only act as the electron flow bridge but also decrease the electrons shift energy obstacle, thus speeding up electrons transfer and achieving effective spatial electron-hole separation. Therefore, a large amount of ·O2– and holes as active species were generated. Remarkably, Bi2O2S/NiFe2O4 establishes a considerably boosted photocatalytic performance for tetracycline degradation (0.032 min–1), which is about 14.2-fold and 7.8-fold of the pristine BOS and NFO, respectively. This work provides a promising motivation for modulating charge transfer by interface control and internal electric field to boost photocatalytic performance.
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