CoTCPP integrates with BiOBr microspheres for improved solar-driven CO2 reduction performance

被引:6
|
作者
Li, Lina [1 ]
Zhang, Yi [1 ]
Liu, Gaopeng [1 ]
Wei, Tiange [1 ]
Zhao, Junze [1 ]
Wang, Bin [1 ]
Ji, Mengxia [1 ]
She, Yuanbin [2 ]
Xia, Jiexiang [1 ]
Li, Huaming [1 ]
机构
[1] Jiangsu Univ, Inst Energy Res, Sch Chem & Chem Engn, 301 Xuefu Rd, Zhenjiang 212013, Peoples R China
[2] Zhejiang Univ Technol, Coll Chem Engn, State Key Lab Breeding Base Green Chem Synth Techn, Hangzhou 310014, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
BiOBr; CoTCPP; CO2; photoreduction; Carriers transfer; adsorption-activation; PHOTOCATALYTIC ACTIVITY; EFFICIENT; PHOTOREDUCTION; MORPHOLOGY; HYBRIDS;
D O I
10.1016/j.gee.2024.01.008
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
CO2 photoreduction into carbon-based chemicals has been considered as an appropriate way to alleviate the energy issue and greenhouse effect. Herein, the 5, 10, 15, 20-tetra (4-carboxyphenyl) porphyrin cobalt (II) (CoTCPP) has been integrated with BiOBr microspheres and formed the CoTCPP/BiOBr composite. The as-prepared CoTCPP/BiOBr-2 composite shows optimized photocatalytic performance for CO2 conversion into CO and CH4 upon irradiation with 300 W Xe lamp, which is 2.03 and 2.58 times compared to that of BiOBr, respectively. The introduced CoTCPP significantly enhanced light absorption properties, promoted rapid separation of photogenerated carriers and boosted the chemisorption of CO2 molecules. The metal Co2+ at the center of the porphyrin molecules also acts as adsorption center for CO2 molecules, accelerating the CO2 conversion into CO and CH4. The possible mechanism of CO2 photoreduction was explored by in-situ FT-IR spectra. This work offers a new possibility for the preparation of advanced photocatalysts. (c) 2024 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:193 / 202
页数:10
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