Abstract

Abstract Endowing materials with specific functions that are not readily available is always of great importance, but extremely challenging. Co 4 N, with its beneficial metallic characteristics, has been proved to be highly active for the oxidation of water, while it is notoriously poor for catalyzing the hydrogen evolution reaction (HER), because of its unfavorable d‐band energy level. Herein, we successfully endow Co 4 N with prominent HER catalytic capability by tailoring the positions of the d‐band center through transition‐metal doping. The V‐doped Co 4 N nanosheets display an overpotential of 37 mV at 10 mA cm −2 , which is substantially better than Co 4 N and even close to the benchmark Pt/C catalysts. XANES, UPS, and DFT calculations consistently reveal the enhanced performance is attributed to the downshift of the d‐band center, which helps facilitate the H desorption. This concept could provide valuable insights into the design of other catalysts for HER and beyond.

Keywords

OverpotentialCatalysisMaterials scienceXANESTransition metalWater splittingHydrogenNanotechnologyDopingBand gapHydrogen fuelDesorptionChemical engineeringPhysical chemistryChemistryOptoelectronicsSpectroscopyPhotocatalysisPhysicsOrganic chemistry

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Publication Info

Year
2018
Type
article
Volume
57
Issue
18
Pages
5076-5080
Citations
1019
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Zhiyan Chen, Yao Song, Jinyan Cai et al. (2018). Tailoring the d‐Band Centers Enables Co<sub>4</sub>N Nanosheets To Be Highly Active for Hydrogen Evolution Catalysis. Angewandte Chemie International Edition , 57 (18) , 5076-5080. https://doi.org/10.1002/anie.201801834

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DOI
10.1002/anie.201801834