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Department of Energy Science and Engineering
Advanced Energy Materials Laboratory
1. Journal Articles
Structural and Electronic Engineering of Co-doped Ni3C Nanoparticles Encapsulated in Ultrathin Carbon Layers for Hydrogen Evolution Reaction
Zhang, Tianyu
;
Wang, Shensong
;
Zhou, Fengling
;
Shanmugam, Sangaraju
;
Kim, Hasuck
;
Zhang, Xinyi
Department of Energy Science and Engineering
Advanced Energy Materials Laboratory
1. Journal Articles
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Title
Structural and Electronic Engineering of Co-doped Ni3C Nanoparticles Encapsulated in Ultrathin Carbon Layers for Hydrogen Evolution Reaction
Issued Date
2023-12
Citation
Zhang, Tianyu. (2023-12). Structural and Electronic Engineering of Co-doped Ni3C Nanoparticles Encapsulated in Ultrathin Carbon Layers for Hydrogen Evolution Reaction. ChemCatChem, 15(23). doi: 10.1002/cctc.202300883
Type
Article
Author Keywords
hydrogen evolution reaction
;
carbon layer
;
nanoparticle
;
stability
;
transition metal carbide
Keywords
BIFUNCTIONAL ELECTROCATALYST
;
WATER ELECTROLYSIS
;
EFFICIENT
;
FILMS
;
MO2C
ISSN
1867-3880
Abstract
With resurgent interest in green hydrogen as a key element in the transition to a renewable-energy economy, developing efficient, earth-abundant, and low-cost catalysts for hydrogen evolution reaction (HER) is becoming increasingly important but is still very challenging. Herein, we report the synthesis of Co-doped Ni3C nanoparticles encapsulated in ultrathin carbon layers (CNCC) by in-situ thermal decomposition of organic-inorganic hybrid as high-performance HER electrocatalysts. Experimental and density functional theory studies evidence that the substantial high-index (113) surfaces in synergy with a few atomic carbon layers contribute significantly to the activity and stability, while the electronic structure of Ni3C is optimized through tuning the Co content to enhance the intrinsic kinetics for HER. The CNCC exhibits excellent HER activities with overpotentials at 10 mA cm−2 (η10) of 102 and 69 mV and Tafel slopes of 74 and 43 mV dec−1 in respective neutral and alkaline media along with a superior stability without noticeable decay up to 100 h. More importantly, the CNCC outperforms the benchmark Pt/C catalyst under high current density (>38 mA cm−2) in an alkaline electrolyte, showing great potential for practical hydrogen production. © 2023 Wiley-VCH GmbH.
URI
http://hdl.handle.net/20.500.11750/47599
DOI
10.1002/cctc.202300883
Publisher
Wiley
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