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Self-assembly of single metal sites embedded covalent organic frameworks into multi-dimensional nanostructures for efficient CO_(2) electroreduction

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摘要 Morphology-controlled electrocatalysts with the ability of CO_(2) adsorption/activation, mass transfer, high stability and porosity are much desired in electrochemical CO_(2) reduction reaction (CO_(2)RR). Here, three kinds of multi-dimensional nanostructures (i.e., hollow sphere, nanosheets and nanofibers) have been successfully produced through the modulation of porphyrin-based covalent organic frameworks (COFs) with various modulators. The obtained nanostructures with high-stability, large surface-area, and single metal sites enable efficient CO_(2)RR into CH_(4). Notably, they all exhibit higher FE (hollow sphere, 68.2%;nanosheet, 64.2% and nanofiber, 71.0%, -0.9 V) than COF-366-Cu (43.0%, -0.9 V) after morphology control. Noteworthy, the FE of COF-366-Cu (HS) keeps higher than 52.4% over a wide potential range from -0.9 V to -1.1 V and the achieved FECH_(4) + C_(2)H_(4) (82.8%, -0.9 V) is superior to most of reported COFs and copper-based electrocatalysts. This work paves a new way in the exploration of COF-based multi-dimensional nanostructures applicable in efficient CO_(2)RR to CH_(4).
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第3期1439-1444,共6页 中国化学快报(英文版)
基金 financially supported by the National Natural Science Foundation of China (NSFC, Nos. 21871141, 21871142,21901122, 22071109 and 92061101) the Natural Science Research of Jiangsu Higher Education Institutions of China (No.19KJB150011) Project funded by China Postdoctoral Science Foundation (Nos. 2018M630572 and 2019M651873) Priority Academic Program Development of Jiangsu Higher Education Institutions and the Foundation of Jiangsu Collaborative Innovation Center of Biomedical Functional Materials。
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