Ultrasmall VN/Co heterostructure with optimized N active sites anchored in N-doped graphitic nanocarbons for boosting hydrogen evolution

Liang-Liang Feng , Dong-Ming Li , Qian-Qian Liu , Chang-Le Fu , Hong-Yan Yin , Li Feng , Yu-Hang Li , Hui Chen , Xiao-Xin Zou
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Abstract

Interface engineering is deemed as an effective approach to optimize the electronic structure of catalytically active sites in electrocatalysts for boosted hydrogen evolution reaction (HER). Herein, a novel ultrasmall VN/Co heterostructure anchored in N-doped graphitized nanocarbons (VN/Co@GNC) is successfully synthesized by a simple calcination protocol. Benefiting from the abundant reactive sites on the interface of ultrasmall heterostructure, enhanced N active sites of VN coupled with Co nanoparticles, as well as excellent conductivity of N-doped graphitized nanocarbons as the scaffold, the resulting VN/Co@GNC material exhibits outstanding electrocatalytic HER performance, delivering the current density of 10 mA/cm2 at a quite low overpotential of 155 mV without iR-compensation, and retaining the catalytic durability for at least 565 h (∼23.5 days) in 1 M KOH solution. The superior catalytic activity and ultrastability of VN/Co@GNC electrocatalyst lay a solid foundation for its commercial applications toward the hydrogen fuel production.

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以N掺杂石墨纳米碳为锚定位点的超小VN/Co异质结构促进析氢
界面工程被认为是优化加速析氢反应电催化剂中催化活性位点电子结构的有效途径。本文通过简单的煅烧方法,成功地合成了一种锚定在n掺杂石墨化纳米碳(VN/Co@GNC)上的新型超小型VN/Co异质结构。得益于超小型异质结构界面上丰富的反应位点、VN与Co纳米粒子偶联的N活性位点增强以及N掺杂石墨化纳米碳作为支架的优异导电性,得到的VN/Co@GNC材料表现出出色的电催化HER性能,在155 mV的过电位下,无需ir补偿,电流密度可达10 mA/cm2。并在1m KOH溶液中保持至少565 h(~ 23.5天)的催化耐久性。VN/Co@GNC电催化剂具有优异的催化活性和超稳定性,为其在氢燃料生产中的商业化应用奠定了坚实的基础。
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