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用硫化镍调制噻吩二羧酸镍骨架微棒阵列的形态和电子结构以实现高效水氧化

Modulation of morphology and electronic structure of nickel thiophenedicarboxylic framework microrod arrays with NiS for efficient water oxidation.

作者信息

Li Zhichao, Du Yuhong, Zuo Gaoshuang, Wang Jin, Wang Chao, Guo Li, Wang Yanzhong

机构信息

School of Materials Science and Engineering, North University of China, Taiyuan 030051, PR China; Shanxi Key Laboratory of Efficient Hydrogen Storage & Production Technology and Application, North University of China, Taiyuan 030051, PR China.

Shanxi Key Laboratory of Efficient Hydrogen Storage & Production Technology and Application, North University of China, Taiyuan 030051, PR China; School of Energy and Power Engineering, North University of China, Taiyuan 030051, PR China.

出版信息

J Colloid Interface Sci. 2025 Dec;699(Pt 2):138209. doi: 10.1016/j.jcis.2025.138209. Epub 2025 Jun 17.

Abstract

Metal-organic frameworks (MOFs) have been a hot topic as oxygen evolution reaction (OER) electrocatalysis owing to their superior specific surface area, plentiful metal active sites and modifiable morphology and composition. Nonetheless, the low electronic conductivity, restricted active sites and lack of structural robustness in MOFs impede their efficacy as catalysts in water electrolysis processes. Herein, nickel thiophenedicarboxylic framework@NiS (Ni-TDC@NiS) composites were prepared on a nickel foam substrate via a two-step hydrothermal method. The results indicate that NiS not only regulates the morphology and local electronic structure of Ni-TDC, but also enhances the structural stability, which leads to the superior OER performance with an overpotential of 220 mV at 10 mA cm, and the Tafel slop of 50.76 mV dec. Furthermore, the assembled overall water electrolysis device with Ni-TDC@NiS and RuNi-TDC as anode and cathode electrodes requires the voltage of only 1.50 V at a current density 10 mA cm, and it can run stably for more than 70 h. This study provides a new idea for enhancing the electronic conductivity of MOF-based electrocatalysts for efficient water oxidation.

摘要

金属有机框架材料(MOFs)因其优异的比表面积、丰富的金属活性位点以及可修饰的形态和组成,成为析氧反应(OER)电催化领域的研究热点。然而,MOFs较低的电子导电性、有限的活性位点以及缺乏结构稳定性,阻碍了它们在水电解过程中作为催化剂的效能。在此,通过两步水热法在泡沫镍基底上制备了镍噻吩二羧酸框架@硫化镍(Ni-TDC@NiS)复合材料。结果表明,硫化镍不仅调节了Ni-TDC的形态和局部电子结构,还增强了结构稳定性,这使得该复合材料在10 mA cm时具有220 mV的过电位和50.76 mV dec的塔菲尔斜率,展现出优异的OER性能。此外,以Ni-TDC@NiS和RuNi-TDC分别作为阳极和阴极电极组装的全水电解装置,在电流密度为10 mA cm时仅需1.50 V的电压,且能稳定运行超过70小时。本研究为提高基于MOF的电催化剂用于高效水氧化的电子导电性提供了新思路。

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