Defective Bi.333(Bi6S9)Br/Bi2S3 heterostructure nanorods: Boosting the activity for efficient visible-light photocatalytic Cr(VI) reduction
Defective Bi.333(Bi6S9)Br/Bi2S3 heterostructure nanorods: Boosting the activity for efficient visible-light photocatalytic Cr(VI) reduction
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有缺陷的 Bi.333(Bi6S9)Br/Bi2S3 异质结构纳米棒:提高有效可见光光催化 Cr(VI) 还原的活性
DOI:
10.1016/j.apcatb.2020.119730
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发表时间:
2021-05
期刊:
影响因子:
--
通讯作者:
贾丽霞
中科院分区:
文献类型:
--
作者:
艾礼莉;王鲁香;徐梦姣;张苏;郭楠楠;贾殿赠;贾丽霞
The design of a direct Z-scheme system heterostructure that can achieve an effective charge separation is highly desirable for photocatalysis. Herein, Bi.333(Bi6S9)Br/Bi2S3heterostructure nanorods were synthesized by a facile hydrothermal method, and the photocatalytic reduction of Cr (VI) under visible light irradiation was conducted to evaluate their photocatalytic performance. Sulfur defects were introduced into the Bi.333(Bi6S9)Br/Bi2S3hybrid nanorods in a controlled way during the phase evolution. Microstructural analysis shows that the interface of Bi.333(Bi6S9)Br/Bi2S3heterostructure consists of (130) facet of Bi.333(Bi6S9)Br and (300) facet of Bi2S3. The high performance of the Bi.333(Bi6S9)Br/Bi2S3hybrid nanorods was ascribed to sulfur defects and direct Z-scheme heterostructure. The sulfur defects can effectively adsorb and activate Cr (VI) while a direct Z-scheme mechanism between Bi.333(Bi6S9)Br and Bi2S3significantly improved the separation and transfer efficiency of photogenerated electrons and holes. This work provides a new strategy for the design of advanced photocatalytic materials.
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影响因子:
15.1
作者:
杨丽君;胡言东;张蕾
通讯作者:
张蕾
DOI:
10.1016/j.apcatb.2020.118602
发表时间:
2020-06
期刊:
Applied Catalysis B: Environmental
影响因子:
--
作者:
Xiong Jie;Li Xibao;Huang Juntong;Gao Xiaoming;Chen Zhi;Liu Jiyou;Li Hai;Kang Bangbang;Yao Wenqing;Zhu Yongfa
通讯作者:
Zhu Yongfa
影响因子:
13.6
作者:
Li, Xibao;Xiong, Jie;Huang, Juntong
通讯作者:
Huang, Juntong
影响因子:
4.9
作者:
Yihui Wu;Bin Zhou;Chi Yang;Xin Zhou;Wen-Hau Zhang
通讯作者:
Yihui Wu;Bin Zhou;Chi Yang;Xin Zhou;Wen-Hau Zhang
影响因子:
22.1
作者:
X. Xiong;Liyong Ding;Qingqian Wang;Yongxiu Li;Q. Jiang;Juncheng Hu
通讯作者:
X. Xiong;Liyong Ding;Qingqian Wang;Yongxiu Li;Q. Jiang;Juncheng Hu