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铁和钼共调制的泡沫镍原位衍生类珊瑚状焦磷酸镍用于析氧反应

Fe and Mo Co-Modulated Coral-like Nickel Pyrophosphate in situ Derived from Nickel-Foam for Oxygen Evolution.

作者信息

Guo Wen, Yang Tao, Zhang Hongyan, Zhou Hao, He Maoshuai, Wei Wenxian, Liang Wenjie, Zhou Yilin, Yu Tingting, Zhao Hong

机构信息

School of Environmental and Chemical Engineering, Jiangsu Key Laboratory of Marine Bioresources and Environment, Jiangsu Key Laboratory of Marine Biotechnology, Jiangsu Ocean University, 222005, Lianyungang, P. R. China.

Co-Innovation Center of Jiangsu Marine Bio-industry Technology, Jiangsu Ocean University, 222005, Lianyungang, P. R. China.

出版信息

ChemSusChem. 2023 Sep 8;16(17):e202300633. doi: 10.1002/cssc.202300633. Epub 2023 Jul 17.

Abstract

A highly active catalyst for the oxygen evolution reaction (OER) is critical to achieve high efficiency in hydrogen generation from water splitting. Direct conversion of nickel foam (NF) into nickel-based catalysts has attracted intensive interest due to the tight interaction of the catalysts to the substrate surface. However, the catalytic performances are still far below expectation because of the problems of low catalyst amount, thin catalyst layer, and small active area caused by the limitations of the synthesis method. Herein, we develop a Fe -induced synthesis strategy to transform the NF surface into a thicker catalyst layer. In addition to the excellent conductivity and high stability, the as-prepared FeMo-Ni P O /NF catalysts expose more active sites and facilitate mass transfer due to their thicker catalyst layer and highly dense coral-like micro-nano structure. Furthermore, the Mo, Fe co-modulation optimizes the adsorption free energies of the OER intermediates, boosting catalytic activities. Its catalytic activity is among the highest, and it exhibits a small Tafel slope of 34.71 mV dec and a low overpotential of 161 mV for delivering a current density of 100 mA cm compared to reported Ni-based catalysts. The present strategy can be further used in the design of other catalysts for energy storage and conversion.

摘要

一种用于析氧反应(OER)的高活性催化剂对于实现高效的水分解制氢至关重要。由于催化剂与基底表面的紧密相互作用,将泡沫镍(NF)直接转化为镍基催化剂引起了广泛关注。然而,由于合成方法的限制导致催化剂用量低、催化剂层薄和活性面积小等问题,其催化性能仍远低于预期。在此,我们开发了一种铁诱导合成策略,将NF表面转化为更厚的催化剂层。除了具有优异的导电性和高稳定性外,所制备的FeMo-Ni P O /NF催化剂由于其更厚的催化剂层和高度致密的珊瑚状微纳结构,暴露出更多的活性位点并促进了传质。此外,Mo、Fe的共调制优化了OER中间体的吸附自由能,提高了催化活性。与已报道的镍基催化剂相比,其催化活性处于最高水平之一,在电流密度为100 mA cm时表现出34.71 mV dec的小塔菲尔斜率和161 mV的低过电位。本策略可进一步用于设计其他用于能量存储和转换的催化剂。

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