Phosphorized polyoxometalate-etched iron-hydroxide porous nanotubes for efficient electrocatalytic oxygen evolution

被引:41
作者
Lin, Hong [1 ]
Wang, Jia-Wei [1 ]
Guo, Xiang-Wei [1 ]
Yao, Shuang [2 ]
Liu, Meng [1 ]
Zhang, Zhi-Ming [1 ]
Lu, Tong-Bu [1 ]
机构
[1] Tianjin Univ Technol, Sch Mat Sci & Engn, Inst New Energy Mat & Low Carbon Technol, Tianjin 300384, Peoples R China
[2] Tianjin Univ Technol, Sch Chem & Chem Engn, Tianjin Key Lab Organ Solar Cells & Photochem Con, Tianjin 300384, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
WATER-OXIDATION CATALYSTS; SELF-TEMPLATE SYNTHESIS; OXIDE; FABRICATION; TRANSITION; NICKEL; PHASE; HETEROSTRUCTURES; MODULATION; ELECTRODES;
D O I
10.1039/c8ta09240k
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
Splitting water into H-2 and O-2 attracts significant attention to meet the increasing need for energy. As the oxygen evolution reaction (OER) constitutes the bottleneck in water splitting, the development of efficient OER catalysts is highly desirable. As a potential electrocatalyst for this reaction, we demonstrate herein a facile two-step method to synthesize FeOOH/FePOx porous nanotubes, which involve the phosphorization of -FeOOH nanotubes that are hydrothermally prepared with the assistance of polyoxometalates (POMs). The acidity of POMs readily modulates the pore size and surface area of the nanotubes. Benefitting from the porous and hollow feature to expose multiple active sites, the FeOOH/FePOx porous nanotubes can be used as a high-performance electrocatalyst, which offers an overpotential of 230 mV at a current density of 10 mA cm(-2) with extraordinary stability in 300 h operation. Its superior performance exceeds that of the commercial catalyst (IrO2, 275 mV) under the same conditions and those of most reported Fe catalysts.
引用
收藏
页码:24479 / 24485
页数:7
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