Interstitial nitrogen modified Rh nanocrystals for efficient and CO-resistant alkaline hydrogen oxidation electrocatalysis

The preparation of active and CO-tolerant platinum-free electrocatalysts toward the hydrogen oxidation reaction (HOR) under alkaline conditions is significant for the practical development of anion exchange membrane fuel cells. Herein, nitrogen atoms are intercalated into the interstitial void of rhodium (N-Rh/C) nanocrystals, which results in electron-deficient and electron-rich Rh sites simultaneously to coordinate the binding energies of multiple key intermediates, achieving highly active and CO-resistant alkaline HOR. <i>In situ</i> surface-enhanced infrared absorption spectroscopy and density functional theory calculations illustrate that the introduction of interstitial N atoms suppresses the electronic back-donation from Rh 4d to the CO 2π* orbital in electron-deficient sites, thereby weakening the CO adsorption and improving CO resistance. Additionally, the enhanced OH adsorption in electron-rich sites can release more free water into the adjacent gap region, increasing water connectivity and hydrogen-bond networks in the electrical double layer and accelerating alkaline HOR kinetics.

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Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc02884a
Citations
3
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
1.09

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article

Interstitial nitrogen modified Rh nanocrystals for efficient and CO-resistant alkaline hydrogen oxidation electrocatalysis

Wei Luo, Qianqian Xiong, Jianchao Yue, Yu Zhang et al.
3 citations
Chemical Science
Electrocatalysts for Energy Conversion
1.09
article

Interstitial nitrogen modified Rh nanocrystals for efficient and CO-resistant alkaline hydrogen oxidation electrocatalysis

Wei Luo, Qianqian Xiong, Jianchao Yue, Yu Zhang, Chaoyi Yang
article en
3 citations

Abstract

The preparation of active and CO-tolerant platinum-free electrocatalysts toward the hydrogen oxidation reaction (HOR) under alkaline conditions is significant for the practical development of anion exchange membrane fuel cells. Herein, nitrogen atoms are intercalated into the interstitial void of rhodium (N-Rh/C) nanocrystals, which results in electron-deficient and electron-rich Rh sites simultaneously to coordinate the binding energies of multiple key intermediates, achieving highly active and CO-resistant alkaline HOR. <i>In situ</i> surface-enhanced infrared absorption spectroscopy and density functional theory calculations illustrate that the introduction of interstitial N atoms suppresses the electronic back-donation from Rh 4d to the CO 2π* orbital in electron-deficient sites, thereby weakening the CO adsorption and improving CO resistance. Additionally, the enhanced OH adsorption in electron-rich sites can release more free water into the adjacent gap region, increasing water connectivity and hydrogen-bond networks in the electrical double layer and accelerating alkaline HOR kinetics.

Chemical ScienceVol. 16(26)
Wuhan University (CN)
Salt Science Research Foundation, National Natural Science Foundation of China, Wuhan University, National Key Research and Development Program of China
Openalex Percentile: Top 24%
Electrocatalysts for Energy Conversion
1.09
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