过电位
析氧
催化作用
化学工程
材料科学
电解水
电解
分解水
铂金
碱性水电解
无机化学
工作(物理)
能量转换
电催化剂
氧气
过程(计算)
电极
化学
制氢
活化能
纳米技术
作者
Hongcen Yang,Kun Zhu,Ganggang Guo,Ying Wang,Wenjie Tan,Hong Zhang,Fei Ma,Shanglong Peng
标识
DOI:10.1021/acsanm.6c00290
摘要
The four-electron transfer process of the oxygen evolution reaction (OER) results in slow kinetics and requires a high overpotential, which significantly increases the energy consumption of the system and reduces its overall efficiency. Herein, the low-crystallinity FeNiOOH support coupled with atomically dispersed platinum (Pt) catalyst is successfully constructed by component optimization and morphology modulation. The obtained Pt 2.08 /Fe 1 Ni 1 OOH catalysts facilitate the transfer of active centers from FeOOH to γ-NiOOH via Pt and significantly reduce the overpotential (200 mV at 10 mA cm –2 ) by dynamically enhancing disorder within the NiOOH structure during the OER process. In addition, Pt 2.08 /Fe 1 Ni 1 OOH catalysts exhibit good HER (145 mV at 10 mA cm –2 ) and ORR (half-wave potential of 0.8 V) performances under alkaline conditions. Meanwhile, Pt 2.08 /Fe 1 Ni 1 OOH maintains minimal loss in a 300 h cycling test in zinc-air batteries. This work provides an effective strategy for developing low-cost and efficient trifunctional electrocatalysts that can be utilized in alkaline water electrolysis and zinc-air batteries.
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