In Situ Pyrolysis of ZIF-67 to Construct Co2N0.67@ZIF-67 for Photocatalytic CO2 Cycloaddition Reaction

被引:25
作者
Jiang, Lingjing [1 ]
Wu, Dengqi [1 ]
Huang, Zishan [1 ]
Chen, Fengfeng [1 ,3 ]
Chen, Kai [2 ]
Ibragimov, Aziz Bakhtiyarovich [4 ]
Gao, Junkuo [1 ]
机构
[1] Zhejiang Sci Tech Univ, Sch Mat Sci & Engn, Lab Funct Porous Mat, Hangzhou 310018, Peoples R China
[2] Zhejiang Prov Innovat Ctr Adv Text Technol, Shaoxing 312000, Peoples R China
[3] Key Lab Green Cleaning Technol & Detergent Zhejian, Lishui 323000, Zhejiang, Peoples R China
[4] Uzbek Acad Sci, Inst Gen & Inorgan Chem, Tashkent 100170, Uzbekistan
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
TRANSITION-METAL; CARBONATES; EVOLUTION; NITRIDES;
D O I
10.1021/acs.inorgchem.4c02504
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The development of heterogeneous catalysts with abundant active sites is pivotal for enhancing the efficiency of photothermal CO2 conversion. Herein, we report the construction of Co2N0.67@ZIF-67 through the in situ pyrolysis of ZIF-67 under low-temperature pyrolysis conditions. During the pyrolysis process, the crystal structure of ZIF-67 is predominantly preserved concurrently with the formation of Co2N0.67 nanoparticles (NPs) within the ZIF-67 pores. The optimal catalyst Co2N0.67@ZIF-67(450,2) not only possesses high photothermal efficiency but also can efficiently activate CO2. Benefiting from these characteristics, Co2N0.67@ZIF-67(450,2) exhibited significant catalytic activity in the photocatalytic cycloaddition of CO2 and epichlorohydrin. The yield of (chloromethyl)ethylene carbonate reached 95%, which is more than 4 times higher than that of ZIF-67 under visible light irradiation (300 W<middle dot>m(2) Xe lamp, 3 h). This study could offer an alternative approach to enhance the photocatalytic activity of MOFs through low-temperature pyrolysis.
引用
收藏
页码:14761 / 14769
页数:9
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