Trimetallic NiFeMo for Overall Electrochemical Water Splitting with a Low Cell Voltage

被引:244
作者
Qin, Fan [1 ]
Zhao, Zhenhuan [2 ,3 ]
Alam, Md Kamrul [1 ]
Ni, Yizhou [4 ,5 ]
Robles-Hernandez, Francisco [3 ,6 ]
Yu, Luo [4 ,5 ]
Chen, Shuo [4 ,5 ]
Ren, Zhifeng [4 ,5 ]
Wang, Zhiming [2 ]
Bao, Jiming [1 ,2 ,3 ]
机构
[1] Univ Houston, Mat Sci & Engn, Houston, TX 77204 USA
[2] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Sichuan, Peoples R China
[3] Univ Houston, Dept Elect & Comp Engn, Houston, TX 77204 USA
[4] Univ Houston, Dept Phys, Houston, TX 77204 USA
[5] Univ Houston, Texas Ctr Superconduct, Houston, TX 77204 USA
[6] Univ Houston, Coll Technol, Houston, TX 77204 USA
基金
美国国家科学基金会;
关键词
LAYERED DOUBLE HYDROXIDE; HYDROGEN EVOLUTION REACTION; BIFUNCTIONAL ELECTROCATALYSTS; HIGHLY EFFICIENT; NICKEL FOAM; NANOWIRE ARRAYS; OXYGEN; MOLYBDENUM; CATALYSTS; PHOSPHIDE;
D O I
10.1021/acsenergylett.7b01335
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
We report the development of an efficient and earth-abundant catalyst for electrochemical overall water splitting. Trimetallic NiFeMo alloy is synthesized by hydrothermal deposition from inorganic precursors and subsequent low-temperature thermal annealing. A complete cell made of NiFeMo electrodes on nickel foam exhibits a low voltage of 1.45 V at 10 mA/cm(2) as a result of low overpotentials for both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). High-resolution transmission electron microscopy reveals that nanometer-sized single-crystal domains of Ni, Fe, and Mo are intimately integrated at the atomic level, which enables a synergistic effect of metallic Ni, Fe, and Mo for efficient HER, while self formed Ni-Fe-Mo (oxy)hydroxides on the surface of the NiFeMo anode become active sites for OER. Such a multimetallic alloy and its (oxy)hydroxides represent a typical HER/OER catalyst couple, and our method provides a new route to develop efficient low-cost metallic alloys for overall water splitting.
引用
收藏
页码:546 / 554
页数:17
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