Maximizing the Formation of Reactive Oxygen Species for Deep Oxidation of NO via Manipulating the Oxygen-Vacancy Defect Position on (BiO)(2)CO3 | |
Rao, Fei1; Zhu, Gangqiang1; Zhang, Weibin2; Xu, Yunhua3; Cao, Baowei3; Shi, Xianjin4; Gao, Jianzhi1; Huang, Yuhong1; Huang, Yu4; Hojamberdiev, Mirabbos5 | |
刊名 | ACS CATALYSIS |
2021-07-02 | |
卷号 | 11期号:13页码:7735-7749 |
关键词 | oxygen vacancy manipulated defect position reactive oxygen species NO removal selectivity |
ISSN号 | 2155-5435 |
DOI | 10.1021/acscatal.1c01251 |
通讯作者 | Zhu, Gangqiang(zgq2006@snnu.edu.cn) |
英文摘要 | Constructing oxygen vacancies (OVs) in metaloxide semiconductors is an effective and simple way to enhance the photocatalytic performance via promoting the utilization of solar light and boosting the formation of surface reactive oxygen species (ROS). The presence of different oxygen atoms in the same crystal structure can possibly lead to the formation of different types of OVs with distinct physicochemical and optoelectronic properties. Particularly, the two different crystallographic positions of oxygen atoms in the [BiO](2)(2+) layer of (BiO)(2)CO3 (BOC) allow the construction of two types of OVs (OVs1 and OVs2). In this work, OVs1-BOC and OVs2-BOC are synthesized via introducing the OVs1 and OVs2 on the surface of the BOC. The influence of OVs1 and OVs2 on the generation of ROS in the BOC is demonstrated based on theoretical and experimental studies by analyzing the separation and redox potentials of photogenerated charge carriers, absorption surface adsorbates (H2O and O-2), and reaction active energy. The photocatalytic performance is evaluated by photo-oxidative nitric oxide (NO) removal efficiency under visible light irradiation. The OVsl-BOC and OVs2-BOC exhibit 50.0 and 41.6% photo-oxidative NO removal efficiencies, while generating 15.6 and 16.54 ppb NO2, respectively. The in situ Fourier transform infrared spectroscopy and estimated NO conversion pathway reveal the photo-oxidative NO removal mechanism and suppression of NO2 formation on the surfaces of OVs1-BOC and OVs2-BOC. This work demonstrates a straightforward approach for enhancing the photo-oxidative NO removal via manipulating the OV defect position in semiconductors. |
资助项目 | National Natural Science Foundation of China[51772183] ; National Natural Science Foundation of China[52072230] ; Key Research and Development Program of Shaanxi Province[2018ZDCXL-SF-02-04] ; Fundamental Research Funds for the Central Universities[2020TS028] |
WOS关键词 | LIGHT PHOTOCATALYTIC PERFORMANCE ; NITROGEN-FIXATION ; BI METAL ; TIO2 ; ADSORPTION ; PHOTOOXIDATION ; MICROSPHERES ; MECHANISMS ; MORPHOLOGY ; NANOSHEETS |
WOS研究方向 | Chemistry |
语种 | 英语 |
出版者 | AMER CHEMICAL SOC |
WOS记录号 | WOS:000670659900010 |
资助机构 | National Natural Science Foundation of China ; Key Research and Development Program of Shaanxi Province ; Fundamental Research Funds for the Central Universities |
内容类型 | 期刊论文 |
源URL | [http://ir.ieecas.cn/handle/361006/16825] |
专题 | 地球环境研究所_粉尘与环境研究室 |
通讯作者 | Zhu, Gangqiang |
作者单位 | 1.Shaanxi Normal Univ, Sch Phys & Informat Technol, Xian 710119, Peoples R China 2.Yangtze Univ, Sch Phys & Optoelect Engn, Jingzhou 434023, Peoples R China 3.Yulin Univ, Sch Chem & Chem Engn, Yulin 719000, Peoples R China 4.Chinese Acad Sci, Inst Earth Environm, State Key Lab Loess & Quaternary Geol SKLLQG, Xian 710061, Peoples R China 5.Tech Univ Berlin, Inst Chem, D-10623 Berlin, Germany |
推荐引用方式 GB/T 7714 | Rao, Fei,Zhu, Gangqiang,Zhang, Weibin,et al. Maximizing the Formation of Reactive Oxygen Species for Deep Oxidation of NO via Manipulating the Oxygen-Vacancy Defect Position on (BiO)(2)CO3[J]. ACS CATALYSIS,2021,11(13):7735-7749. |
APA | Rao, Fei.,Zhu, Gangqiang.,Zhang, Weibin.,Xu, Yunhua.,Cao, Baowei.,...&Hojamberdiev, Mirabbos.(2021).Maximizing the Formation of Reactive Oxygen Species for Deep Oxidation of NO via Manipulating the Oxygen-Vacancy Defect Position on (BiO)(2)CO3.ACS CATALYSIS,11(13),7735-7749. |
MLA | Rao, Fei,et al."Maximizing the Formation of Reactive Oxygen Species for Deep Oxidation of NO via Manipulating the Oxygen-Vacancy Defect Position on (BiO)(2)CO3".ACS CATALYSIS 11.13(2021):7735-7749. |
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