Cr-doped NiFe sulfides nanoplate array: Highly efficient and robust bifunctional electrocatalyst for the overall water splitting and seawater electrolysis

被引:9
作者
He, Yujia [1 ]
Yang, Xuan [1 ]
Jiang, Mingyuan [1 ]
Liu, Fuguang [1 ]
Zhang, Jinming [1 ]
Li, Huiying [1 ]
Cui, Liang [2 ]
Xu, Jiangtao [1 ]
Ji, Xuqiang [1 ]
Liu, Jingquan [1 ,2 ]
机构
[1] Qingdao Univ, Inst Graphene Appl Technol Innovat, Coll Mat Sci & Engn, Qingdao 266071, Peoples R China
[2] Linyi Univ, Coll Mat Sci & Engn, Linyi 276000, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
NiFeCrSx/NF; Seawater hydrolysis; Trimetallic synergy; Cr dopping; Self-supporting catalysts; OXYGEN-EVOLUTION ELECTROCATALYSTS; HIGH-PERFORMANCE; CATHODE;
D O I
10.1016/j.jcis.2024.11.072
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
To replace precious metals and reduce production costs for large-scale hydrogen production, developing stable, high-performance transition metal electrocatalysts that can be used in a wide range of environments is desirable yet challenging. Herein, a self-supported hybrid catalyst (NiFeCrSx/NF) with high electrocatalytic activity was designed and constructed using conductive nickel foam as a substrate via manipulation of the cation doping ratio of transition metal compounds. Due to the strong coupling synergy between the metal sulfides NiS2, Fe9S11, and Cr2S3, as well as their interaction with the conductive nickel foam (NF), the energy barrier for catalytic reactions is reduced, and the charge transfer rate is enhanced. This significantly improves the hydrogen evolution reaction (HER) performance of NiFeCrSx/NF, achieving a current density of 10 mA cm-2 with an overpotential of just 66 mV. Furthermore, doping with chromium generates different valence states of Cr during the catalytic process, which can synergize with the high-valent Fe and Ni, promoting the formation of oxygen vacancies and enriching the active sites for the oxygen evolution reaction (OER). Consequently, at a current density of 10 mA cm-2 in 1.0 M KOH, the overpotential for OER is only 223 mV for NiFeCrSx/NF. Additionally, the in situ grown of self supporting nanoflower structure on NiFe-LDH not only provides a large catalytic surface area but also facilitates electrolyte penetration during the catalytic process, endowing NiFeCrSx/NF with high long-term stability. When used as a bifunctional catalyst for overall water splitting, the NiFeCrSx/NF||NiFeCrSx/NF electrolyzer requires only 1.29 V to deliver a current density of 10 mA cm- 2. Simultaneously, Cr doping protects the Fe sites by maintaining stable valence states, ensuring high performance and stability of NiFeCrSx/NF, even when it is utilized for seawater splitting. This strategy offers novel concepts for creating catalysts based on non-precious metals that can be utilized in various application scenarios.
引用
收藏
页码:1079 / 1089
页数:11
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