In situ post-modification of substoichiometric 2D conjugated MOFs to boost ethylene selectivity in electrocatalytic CO2 reduction

被引:4
作者
Li, Yijun [1 ]
Lv, Jianning [1 ]
Li, Shuai [1 ]
Dai, Lu [1 ]
Wang, Bo [1 ,3 ]
Li, Pengfei [1 ,2 ,3 ]
机构
[1] Beijing Inst Technol, Minist Educ, Sch Chem & Chem Engn, Frontiers Sci Ctr High Energy Mat,Key Lab Cluster, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Adv Res Inst Multidisciplinary Sci, 6,Jinfeng Rd, Zhuhai 519088, Peoples R China
[3] Beijing Inst Technol, Adv Technol Res Inst Jinan, Jinan 250300, Peoples R China
基金
中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; FUNCTIONALIZATION; POLYMERIZATION; CONVERSION; CATALYSTS;
D O I
10.1039/d4ta04011b
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
2D conjugated MOFs (2D c-MOFs) have attracted significant interest in electrocatalysis due to their intrinsic electrical conductivity. Their catalytic performance heavily relied on the metal centers and structures of highly fused polyaromatic hydrocarbon ligands. This led to a considerable challenge in fine-tuning the catalytic performance of 2D c-MOFs. Thus, the modulation of the catalytic performance of 2D c-MOFs through chemical modification has been less explored. Herein, the peripheral defects of substoichiometric 2D c-MOFs are capped with 2,3,5,6-tetrafluoroterephthalonitrile at different doping levels via a facile one-pot post-synthetic strategy. Introducing capping groups not only displays a profound impact on the physical properties of 2D c-MOF but also leads to an enhanced electrocatalytic CO2 reduction to C2H4 with an FE of 54% at -1.2 V vs. RHE. Tuning the catalytic performance of 2D c-MOFs with the chemical modification strategy would notably expand the potential application of 2D c-MOFs.
引用
收藏
页码:24549 / 24555
页数:7
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