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Cl-诱导的含氧空位原子层厚Bi2WO6的可控合成及其深度氧化NO性能
引用本文:杨祥龙,汪圣尧,陈婷,杨楠,江开,汪佩,李淑,丁星,陈浩. Cl-诱导的含氧空位原子层厚Bi2WO6的可控合成及其深度氧化NO性能[J]. 催化学报, 2021, 42(6): 1013-1023,中插37-中插45. DOI: 10.1016/S1872-2067(20)63708-1
作者姓名:杨祥龙  汪圣尧  陈婷  杨楠  江开  汪佩  李淑  丁星  陈浩
作者单位:华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070;华中农业大学理学院, 环境食品教育部重点实验室, 湖北武汉430070
基金项目:国家自然科学基金;the Natural Science Foundation of Hubei Province ;中央高校基本科研业务费专项基金;This work was supported by the National Natural Science Foundation of China ;湖北省自然科学基金;and Fundamental Research Funds for the Central Universities
摘    要:开发具有高量子效率的半导体光催化材料是极具前景的解决能源短缺和环境污染问题的策略.在已报道的诸多光催化材料中,超薄二维(2D)材料表现突出,凭借其高效的载流子分离传输性能备受研究者的青睐.然而,苛刻的合成条件、缺乏表面活性位点等问题制约了其应用.因此,温和可控地合成具有大量活性位点的原子层厚2D材料具有重要的意义.作为...

关 键 词:氧空位  原子层厚Bi2WO6  氯离子  光催化  NO氧化

Chloridion-induced dual tunable fabrication of oxygen-deficient Bi2WO6 atomic layers for deep oxidation of NO
Xianglong Yang,Shengyao Wang,Ting Chen,Nan Yang,Kai Jiang,Pei Wang,Shu Li,Xing Ding,Hao Chen. Chloridion-induced dual tunable fabrication of oxygen-deficient Bi2WO6 atomic layers for deep oxidation of NO[J]. Chinese Journal of Catalysis, 2021, 42(6): 1013-1023,中插37-中插45. DOI: 10.1016/S1872-2067(20)63708-1
Authors:Xianglong Yang  Shengyao Wang  Ting Chen  Nan Yang  Kai Jiang  Pei Wang  Shu Li  Xing Ding  Hao Chen
Affiliation:(College of Science,Key Laboratory of Environment Correlative Dietology of Ministry of Education,Huazhong Agricultural University,Wuhan 430070,Hubei,China)
Abstract:Engineering an efficient interface is a trustworthy strategy for designing advanced photocatalytic systems for solar energy conversion. Herein, oxygen-deficient Bi2WO6 atomic layers without organic residues were successfully fabricated via a facile solvothermal strategy by the multifunctional regu-latory mechanism of introduced chloridion. Both DFT calculations and speciation determination revealed that chloridion displayed a more pronounced effect in the controllable synthesis of oxy-gen-deficient Bi2WO6 atomic layers without organic residues: ultrathinning and defect-engineering. This built-in multi-cooperative interface endowed Bi2WO6 with intriguing photoelectrochemical properties, O2 activation ability, and ultrahigh activity in visible-light powered deep oxidation of NO. A reasonable photocatalytic mechanism was proposed based on in situ infrared spectroscopy analy-sis and theoretical calculations. We believe that this multi-cooperative interface engineering of oxygen-deficient Bi2WO6 atomic layers without organic residues could provide new insights into the design of two-dimensional (2D) layered materials with efficient active sites and pave the way for efficient NO photooxidation systems.
Keywords:Oxygen vacancy  Bi2WO6 atomic layers  Chloridion  Photocatalysis  NO oxidation
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