Amino group promoted photoelectrocatalytic CO2 reduction activity observed in mixed-linker Cu-based metal-organic frameworks

被引:2
|
作者
Lei, Chengkun [1 ,2 ]
Luo, Man [1 ,2 ]
Li, Huimin [1 ,2 ]
Shen, Qianqian [1 ,2 ]
Liu, Xuguang [1 ,2 ]
Jia, Husheng [1 ,2 ,3 ]
Xue, Jinbo [1 ,2 ]
机构
[1] Taiyuan Univ Technol, Key Lab Interface Sci & Engn Adv Mat, Minist Educ, Taiyuan 030024, Peoples R China
[2] Taiyuan Univ Technol, Coll Mat Sci & Engn, Taiyuan 030024, Peoples R China
[3] Shanxi Zheda Inst Adv Mat & Chem Engn, Taiyuan 030032, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
PHOTOCATALYTIC ACTIVITY; PHOTOREDUCTION; STABILITY; MOFS;
D O I
10.1007/s10854-023-10644-y
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
The absorption of visible light of mixed-linker metal-organic frameworks can be enhanced by adding organic ligands to be present as reaction sites. In this work, through the introduction of an amino-functionalized organic ligand (NH2BDC, BDC = 1, 4-benzenedicarboxylate) into the structure of CuBDC, dual-ligand Cu-based MOF (CuBDC-xNH(2)/CF, x represents the molar ratio of NH2BDC) was successfully synthesized on copper foam (CF). The photoelectrocatalytic CO2 reduction performance of all samples was explored when increasing amounts of NH2BDC linkers (0%, 5%, 10%, 20%, 50%, and 100%) are incorporated in the framework. The highest Faradaic efficiency of CO (51.5%) was achieved when the molar ratio of NH2BDC was 10%. NH2BDC can effectively improve the visible light absorption ability of MOFs. And both terephthalic acid (H2BDC) and NH2BDC are coordinated with Cu-O clusters, which contribute to the generation and separation of charges. At the same time, the amino functional group can effectively adsorb the CO2 molecules as a basic site. The synergistic effect improves the Faradaic efficiency of the reduction products.
引用
收藏
页数:12
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