Large-Scale and Simple Synthesis of NiFe(OH)x Electrode Derived from Raney Ni Precursor for Efficient Alkaline Water Electrolyzer

被引:2
|
作者
Li, Tianshui [1 ]
Liu, Wei [1 ]
Xin, Huijun [1 ]
Sha, Qihao [1 ]
Xu, Haijun [2 ]
Kuang, Yun [1 ,3 ]
Sun, Xiaoming [1 ]
机构
[1] Univ Chem Technol, Coll Chem, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Beijing Univ Chem Technol, Coll Math & Phys, Beijing 100029, Peoples R China
[3] Tsinghua Univ Shenzhen, Ocean Hydrogen Energy R&D Ctr, Res Inst, Shenzhen 518033, Peoples R China
关键词
oxygen evolution reaction; large-scale electrode; alkaline water electrolysis; OXYGEN EVOLUTION; ENERGY;
D O I
10.3390/catal14050296
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Water electrolysis is a crucial technology in the production of hydrogen energy. Due to the escalating industrial demand for green hydrogen, the required electrode size for a traditional alkaline water electrolyzer has been increasing. Numerous studies have focused on developing highly active oxygen evolution reaction (OER) catalysts for water electrolysis. However, there remains a significant gap between the microscale synthesis of catalysts in laboratory settings and the macroscale preparation required for industrial scenarios. This challenge is particularly pronounced in the synthesis of sizable self-supported electrodes. In this work, we employed a commercially available Raney Ni-coated Ni mesh as a precursor material to fabricate a self-supported NiFe(OH)(x)@Raney Ni anode with a substantial dimension exceeding 300 mm through a straightforward immersion technique. The as-prepared electrode exhibited remarkable electrocatalytic OER activity, as an overpotential of only 240 mV is required to achieve 10 mA cm(-2). This performance is comparable to that of NiFe-LDHs synthesized via a hydrothermal method, which is difficult to scale up for industrial applications. Furthermore, the electrode demonstrated exceptional durability, maintaining stable operation for over 100 h at a current density of 500 mA cm(-2). The large-scale electrode displayed consistent overpotentials across various areas, indicating uniform catalytic activity. When integrated into an alkaline water electrolysis device, it delivered an average cell voltage of 1.80 V at 200 mA cm(-2) and achieved a direct current hydrogen production energy consumption as low as 4.3 kWh/Nm(3). These findings underline the suitability of electrodes for industrial scale applications, offering a promising alternative for energy-efficient hydrogen production.
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页数:12
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