Interfacial microenvironment modulation enhancing catalytic kinetics of bimetallic (oxy)hydroxide heterostructures for highly efficient oxygen evolution reaction

被引:6
|
作者
Yang, Yang [1 ]
Lin, Meihong [1 ]
Song, Yunhua [1 ]
Tuerhong, Gulinigaer [1 ]
Dai, Jiaqi [1 ]
Zhang, Tao [1 ]
Guo, Donggang [2 ]
Liu, Lu [1 ]
机构
[1] Nankai Univ, Coll Environm Sci & Engn, Tianjin Key Lab Environm Remediat & Pollut Contro, 38 Tongyan Rd, Tianjin 300350, Peoples R China
[2] Shanxi Univ, Coll Environm & Resource, Shanxi Lab Yellow River, 92 Wucheng Rd, Taiyuan 030006, Shanxi, Peoples R China
关键词
Heterostructure; Interface engineering; Seawater splitting; Oxygen evolution reaction; Ni(OH)2; FeOOH; DOPED CARBON; PERFORMANCE; NANOPARTICLES; ELECTROCATALYSTS;
D O I
10.1016/j.jallcom.2022.164879
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 splitting is a promising hydrogen production technology limited by the slow kinetic oxygen evolution reaction (OER). The development of highly active and robust OER catalysts is in high demand. A series of three-dimensional (3D) self-supported FeOOH@Ni(OH)2 heterostructures supported on nickel foam are synthesized and used as efficient OER catalysts using a simple hydrothermal method. The benefits of the appropriate 3D nanoflower morphology, the large number of FeOOH nanosheets adhered on the nanoflower surface, the formation of heterogeneous interfaces, and the synergistic effect of Ni(OH)2 and FeOOH significantly improve the OER catalytic performance of the material. The optimal catalyst in 1 M KOH, alkaline artificial seawater (1 M KOH + 1 M NaCl), and alkaline nature seawater (1 M KOH + seawater) require only 285, 286, and 325 mV overpotential, respectively, to achieve 100 mA cm-2 current density and has robust stability. This study contributes to the rational design of interface-engineered heterostructures for seawater splitting by synthesizing high catalytic activity catalysts.
引用
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页数:8
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