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Hydrogen-Bonded Organic Framework Supporting Atomic Bi-NO Sites for High-Efficiency Electrocatalytic CO Reduction. | LitMetric

Hydrogen-Bonded Organic Framework Supporting Atomic Bi-NO Sites for High-Efficiency Electrocatalytic CO Reduction.

Angew Chem Int Ed Engl

Key Laboratory of Cluster Science Ministry of Education, Beijing Key Laboratory of Photoelectronic/Electrophotonic Conversion Materials, Advanced Technology Research Institute (Jinan), Advanced Research Institute of Multidisciplinary Science, School of Materials Science and Engineering, School of Chemistry and Chemical Engineering, Beijing Institute of Technology, No. 5, South Street, Zhongguancun, Haidian District, Beijing, 100081, China.

Published: May 2024

AI Article Synopsis

Article Abstract

Single atomic catalysts (SACs) offer a superior platform for studying the structure-activity relationships during electrocatalytic CO reduction reaction (CORR). Yet challenges still exist to obtain well-defined and novel site configuration owing to the uncertainty of functional framework-derived SACs through calcination. Herein, a novel Bi-NO site supported on the (1 1 0) plane of hydrogen-bonded organic framework (HOF) is reported directly for CORR. In flow cell, the target catalyst Bi1-HOF maintains a faradaic efficiency (FE) HCOOH of over 90 % at a wide potential window of 1.4 V. The corresponding partial current density ranges from 113.3 to 747.0 mA cm. And, Bi1-HOF exhibits a long-term stability of over 30 h under a successive potential-step test with a current density of 100-400 mA cm. Density function theory (DFT) calculations illustrate that the novel Bi-NO site supported on the (1 1 0) plane of HOF effectively induces the oriented electron transfer from Bi center to CO molecule, reaching an enhanced CO activation and reduction. Besides, this study offers a versatile method to reach series of M-NO sites with regulable metal centers via the same intercalation mechanism, broadening the platform for studying the structure-activity relationships during CORR.

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Source
http://dx.doi.org/10.1002/anie.202404015DOI Listing

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