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通过负载铂簇的镍铁钴磷化物催化实现1000小时稳定的海水电解产生安培级氢气。

Ampere-Level Hydrogen Generation via 1000 H Stable Seawater Electrolysis Catalyzed by Pt-Cluster-Loaded NiFeCo Phosphide.

作者信息

Zhou Linlin, Wan Tong, Zhong Yang, Liu Wei, Yu Linfeng, Li Tianshui, Sun Kai, Waterhouse Geoffrey I N, Xu Haijun, Kuang Yun, Zhou Daojin, Sun Xiaoming

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing, 100029, China.

Weichai Power Co., Ltd., Weifang, 261061, China.

出版信息

Small. 2024 Dec;20(49):e2406076. doi: 10.1002/smll.202406076. Epub 2024 Sep 17.

Abstract

Seawater electrolysis can generate carbon-neutral hydrogen but its efficiency is hindered by the low mass activity and poor stability of commercial catalysts at industrial current densities. Herein, Pt nanoclusters are loaded on nickel-iron-cobalt phosphide nanosheets, with the obtained Pt@NiFeCo-P electrocatalyst exhibiting excellent hydrogen evolution reaction (HER) activity and stability in alkaline seawater at ampere-level current densities. The catalyst delivers an ultralow HER overpotential of 19.7 mV at -10 mA cm in seawater-simulating alkaline solutions, along with a Pt-mass activity 20.8 times higher than Pt/C under the same conditions, while dropping to 8.3 mV upon a five-fold NaCl concentrated natural seawater. Remarkably, Pt@NiFeCo-P offers stable operation for over 1000 h at 1 A cm in an alkaline brine electrolyte, demonstrating its potential for efficient and long-term seawater electrolysis. X-ray photoelectron spectroscopy (XPS), in situ electrochemical impedance spectroscopy (EIS), and in situ Raman studies revealed fast electron and charge transfer from the NiFeCo-P substrate to Pt nanoclusters enabled by a strong metal-support interaction, which increased the coverage of H and accelerated water dissociation on high valent Co sites. This study represents a significant advancement in the development of efficient and stable electrocatalysts with high mass activity for sustainable hydrogen generation from seawater.

摘要

海水电解能够产生碳中和氢气,但其效率受到工业电流密度下商业催化剂的低质量活性和较差稳定性的阻碍。在此,将铂纳米团簇负载在镍铁钴磷化物纳米片上,所制备的Pt@NiFeCo-P电催化剂在碱性海水中安培级电流密度下表现出优异的析氢反应(HER)活性和稳定性。在模拟海水的碱性溶液中,该催化剂在-10 mA cm时的HER过电位超低,仅为19.7 mV,同时在相同条件下其铂质量活性比Pt/C高20.8倍,而在五倍氯化钠浓缩的天然海水中过电位降至8.3 mV。值得注意的是,Pt@NiFeCo-P在碱性盐水电解质中1 A cm下可稳定运行超过1000小时,展现了其用于高效长期海水电解的潜力。X射线光电子能谱(XPS)、原位电化学阻抗谱(EIS)和原位拉曼研究表明,通过强金属-载体相互作用实现了从NiFeCo-P基底到铂纳米团簇的快速电子和电荷转移,这增加了H的覆盖率并加速了高价钴位点上的水离解。这项研究代表了在开发具有高质量活性的高效稳定电催化剂以实现可持续海水制氢方面的重大进展。

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