Co,N-Codoped porous vanadium nitride nanoplates as superior bifunctional electrocatalysts for hydrogen evolution and oxygen reduction reactions

Zhang, N; Cao, L; Feng, L; Huang, J; Kajiyoshi, K; Li, C; Liu, Q; Yang, D; He, J

HERO ID

6308189

Reference Type

Journal Article

Year

2019

Language

English

PMID

31165119

HERO ID 6308189
In Press No
Year 2019
Title Co,N-Codoped porous vanadium nitride nanoplates as superior bifunctional electrocatalysts for hydrogen evolution and oxygen reduction reactions
Authors Zhang, N; Cao, L; Feng, L; Huang, J; Kajiyoshi, K; Li, C; Liu, Q; Yang, D; He, J
Journal Nanoscale
Volume 11
Issue 24
Page Numbers 11542-11549
Abstract Developing efficient and low-cost bifunctional electrocatalysts as candidates for Pt-based materials to satisfy commercial applications in the hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) is still very challenging. Herein, we show that Co,N-codoped porous vanadium nitride (VCoN) nanoplates are successfully synthesized via a simple one-step pyrolysis protocol without the use of NH3 gas. We also demonstrate that the crystallization, surface chemical state and porosity of vanadium nitride are well modulated by inventively using Co dopants as structural inducers. The resulting VCoN material exhibits an excellent catalytic activity towards the HER in alkaline media, with an extremely low onset potential of -0.03 V, an overpotential of 179 mV at 10 mA cm-2, and a remarkable durability for over 100 h. Moreover, it shows a superior ORR performance, which compares favorably with commercial 20% Pt/C, exhibiting an onset potential of ∼1.02 V, a half-wave potential of ∼0.91 V and a weak potential shift (-5 mV) after 2000 cycles at 1600 rpm in 0.1 M KOH. Such excellent electrocatalytic performance primarily contributes to the unique structural features of the heteroatom N (pyrrolic and graphitic N) and Co codoping in favor of improving the electrical conductivity and the high porosity contributing to exposing numerous catalytic active sites.
Doi 10.1039/c9nr02637a
Pmid 31165119
Wosid WOS:000472559800012
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English