Electronic tailoring of Ni–NbB2 nanorods via molten salt synthesis for high-efficiency alkaline hydrogen evolution

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Yuhui Sun, Bozhen Li, Jihui Lang, Guangbo Che, Yuanyuan Wu and Mengxiang Shang
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Abstract

The design of efficient and durable electrocatalysts for enhancing the kinetics of the hydrogen evolution reaction (HER) in alkaline water electrolysis is a significant challenge. Borides have attracted extensive attention due to their excellent corrosion resistance and unique structures. In this study, NbB2 was synthesized by the molten salt method, and then a metal nickel source was incorporated into the synthesized NbB2 to prepare a nickel-doped NbB2 electrocatalyst (Ni–NbB2) with a nanorod structure. Notably, Ni–NbB2 exhibited an overpotential of only 239 mV at a current density of 10 mA cm−2, significantly lower than that of pure NbB2 (562 mV), and also demonstrated long-term stability. The doping of metal nickel regulated the electronic structure of the metal Nb on the catalyst surface, accelerating the kinetics of the HER reaction. Moreover, the doping of Ni increased the number of catalytic active sites, promoting the full contact between the electrolyte and the catalytic reaction sites and accelerating the charge transfer rate. These findings open up new possibilities for enhancing the HER catalytic activity of metal borides through the strategy of heterometal doping.

Abstract Image

熔盐法制备Ni-NbB2纳米棒的电子裁剪及高效碱氢析出
设计高效耐用的电催化剂来提高碱水电解中析氢反应的动力学是一个重大的挑战。硼化物以其优异的耐腐蚀性和独特的结构引起了人们的广泛关注。本研究采用熔盐法合成NbB2,然后在合成的NbB2中加入金属镍源,制备出纳米棒结构的掺镍NbB2电催化剂(Ni-NbB2)。值得注意的是,Ni-NbB2在电流密度为10 mA cm−2时的过电位仅为239 mV,明显低于纯NbB2的过电位(562 mV),并且具有长期稳定性。金属镍的掺杂调节了金属Nb在催化剂表面的电子结构,加速了HER反应的动力学。此外,Ni的掺杂增加了催化活性位点的数量,促进了电解质与催化反应位点之间的充分接触,加快了电荷转移速率。这些发现为通过异金属掺杂策略提高金属硼化物的HER催化活性开辟了新的可能性。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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