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负载钼酸镍磷化的钒掺杂镍微球有助于增强电子转移以实现稳定的全水分裂。

Vanadium-doped Ni microspheres loaded with phosphatization of NiMoO contributing to enhanced electron transfer for stable overall water splitting.

作者信息

Qin Ruige, Chi Linyuan, Han Chengdong, Wang Wenquan, Li Yutong, Xie Chenxu, Zhao Lijun, Lang Xingyou, Jiang Qing

机构信息

Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.

Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.

出版信息

J Colloid Interface Sci. 2024 Jun 15;664:13-24. doi: 10.1016/j.jcis.2024.02.204. Epub 2024 Mar 5.

Abstract

At present, there are few reports on the micron-sized catalysts for overall water splitting. In this study, phosphating method were used to construct the self-supporting catalyst (V doped Ni microspheres coated by NiMoO/NiP) with microspherical structure, providing a short path and a stable structure to guarantee quick electron transfer and excellent catalytic performance. Hence, oxygen evolution reaction (OER) only needs 254 mV to reach a current density of 50 mA cm in 1.0 mol/L KOH, after 114 h without attenuation. The catalyst can achieve a current densitiy of 10 mA cm with a voltage of only 158 mV for hydrogen evolution reaction (HER). When micron scale V-Ni@NiMoO/NiP is used as both anode and cathode for overall water splitting, the device can operate at a current density of 10 mA cm for more than 200 h of good stability. Its superior catalytic performance can be attributed to the construction of micron size and phosphating. DFT calculations indicate that the introduction of P better activates the adsorbed OH and HO, reduces reaction the energy barrier, and improves the catalytic activity.

摘要

目前,关于用于全水分解的微米级催化剂的报道较少。在本研究中,采用磷化方法构建了具有微球结构的自支撑催化剂(NiMoO/NiP包覆的V掺杂Ni微球),提供了短路径和稳定结构,以确保快速的电子转移和优异的催化性能。因此,在1.0 mol/L KOH中,析氧反应(OER)仅需254 mV即可达到50 mA/cm²的电流密度,在114 h后无衰减。该催化剂在析氢反应(HER)中,仅需158 mV的电压就能实现10 mA/cm²的电流密度。当微米级V-Ni@NiMoO/NiP用作全水分解的阳极和阴极时,该装置可在10 mA/cm²的电流密度下稳定运行超过200 h。其优异的催化性能可归因于微米尺寸的构建和磷化处理。密度泛函理论(DFT)计算表明,P的引入更好地活化了吸附的OH和HO,降低了反应能垒,提高了催化活性。

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