Guanine-derived carbon nanosheet encapsulated Ni nanoparticles for efficient CO electroreduction.

Dalton Trans

Key Laboratory of Advanced Carbon-Based Functional Materials (Fujian Province University), Fuzhou University, Fuzhou 350016, Fujian, China.

Published: June 2024

AI Article Synopsis

  • The study focuses on creating a new electrocatalyst, specifically a nitrogen-doped carbon shell-coated nickel nanoparticle, to improve carbon dioxide reduction efficiency to carbon monoxide.
  • The optimal catalyst, Ni@NC-1000, achieves over 90% faradaic efficiency at various potentials and a maximum of 95.6% at -0.75 V (RHE), maintaining stable performance for 20 hours.
  • Its effectiveness is linked to the presence of active pyrrolic nitrogen sites, which help in activating CO and lowering the energy barrier for COOH generation, presenting a promising strategy for developing efficient electrochemical catalysts.

Article Abstract

Developing novel electrocatalysts for achieving high selectivity and faradaic efficiency in the carbon dioxide reduction reaction (CORR) poses a major challenge. In this study, a catalyst featuring a nitrogen-doped carbon shell-coated Ni nanoparticle structure is designed for efficient carbon dioxide (CO) electroreduction to carbon monoxide (CO). The optimal Ni@NC-1000 catalyst exhibits remarkable CO faradaic efficiency (FE) values exceeding 90% across a broad potential range of -0.55 to -0.9 V ( RHE), and attains the maximum FE of 95.6% at -0.75 V ( RHE) in 0.5 M NaHCO. This catalyst exhibits sustained carbon dioxide electroreduction activity with negligible decay after continuous electrolysis for 20 h. More encouragingly, a substantial current density of 200.3 mA cm is achieved in a flow cell at -0.9 V (. RHE), reaching an industrial-level current density. Fourier transform infrared spectroscopy and theoretical calculations demonstrate that its excellent catalytic performance is attributed to highly active pyrrolic nitrogen sites, promoting CO activation and significantly reducing the energy barrier for generating *COOH. To a considerable extent, this work presents an effective strategy for developing high-efficiency catalysts for electrochemical CO reduction across a wide potential window.

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Source
http://dx.doi.org/10.1039/d4dt00495gDOI Listing

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