Enhanced photocatalytic nitrogen fixation performance via in situ constructing BiO2-x/NaNbO3 heterojunction

被引:2
|
作者
Zhang, Jiayu [1 ]
Zeng, Zhihao [1 ]
Yue, Lin [1 ]
Zhao, Chunran [3 ]
Hu, Xin [1 ]
Zhao, Leihong [1 ]
Wang, Xiuwen [2 ]
He, Yiming [1 ,3 ]
机构
[1] Zhejiang Normal Univ, Coll Chem & Mat Sci, Key Lab, Minist Educ Adv Catalysis Mat, Jinhua 321004, Peoples R China
[2] Qiqihar Univ, Sch Chem & Chem Engn, Heilongjiang Prov Key Lab Surface Act Agent & Auxi, Qiqihar 161006, Peoples R China
[3] Zhejiang Normal Univ, Dept Mat Sci & Engn, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalyst; Solar energy; Hydrothermal; BiO2-x/NaNbO3; Photocatalytic N-2-fixation; WATER; NANOSHEETS; DOTS;
D O I
10.1016/j.cjche.2024.02.003
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The fabrication of heterojunction catalysts is an effective strategy to enhance charge separation efficiency, thereby boosting the performance of photocatalysts. In this study, BiO2-x nanosheets were synthesized through a hydrothermal process and loaded onto NaNbO3 microcube to construct a series of BiO2-x/NaNbO3 heterojunctions for photocatalytic N-2 fixation. Results indicated that 2.5% BiO2-x/NaNbO3 had the highest photocatalytic performance. The NH3 production rate under simulated solar light reached 406.4 mu mol center dot L-1 center dot g(-1)center dot h(-1), which reaches 2.6 and 3.8 times that of NaNbO3 and BiO2-x, respectively. BiO2-x nanosheets primarily act as electron trappers to enhance the separation efficiency of charge carriers. The strong interaction between BiO2-x and NaNbO3 facilitates the electron migration between them. Meanwhile, the abundant oxygen vacancies in BiO2-x nanosheets may facilitate the adsorption and activation of N-2, which may be another possible reason of the high photocatalytic activity of the BiO2-x/NaNbO3. This study may offer new insights for the development of semiconductor materials in photocatalytic nitrogen fixation. (c) 2024 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd. All rights reserved.
引用
收藏
页码:92 / 100
页数:9
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