过电位
电催化剂
析氧
双功能
分解水
化学工程
材料科学
纳米棒
阳极
电解
电解水
阴极
热液循环
电流密度
催化作用
无机化学
电化学
纳米技术
电极
化学
电解质
光催化
物理化学
物理
工程类
量子力学
生物化学
作者
Sathyanarayanan Shanmugapriya,Subramani Surendran,Dae Jun Moon,Joon Young Kim,Hyunjung Lee,Sebastian Cyril Jesudass,Krishnan Veeramani,Shivraj Mahadik,Gnanaprakasam Janani,Hyeonuk Choi,Il Kim,Philipp Jung,Jaeyeong Heo,Kootak Hong,Yong Il Park,Uk Sim
标识
DOI:10.1016/j.ijhydene.2023.11.307
摘要
Oxygen evolution reaction (OER) is the bottleneck for effective overall water splitting owing to its sluggish reaction kinetics. Metal oxyhydroxides are a significant class of electrocatalysts that demonstrate remarkable activity and stability toward the oxygen evolution reaction. A facile one-pot hydrothermal synthesis is demonstrated in this study to obtain the heterostructured NiFe-oxyhydroxide electrocatalyst. FeOOH nanorods are decked over the 2D Ni(OH)2NiOOH nanosheets to form the Ni(OH)2NiOOH/FeOOH heterostructure. The prepared Ni(OH)2NiOOH/FeOOH electrocatalyst demands a minimal OER overpotential of 209 mV to reach a current density of 10 mA cm−2, which is relatively smaller than the commercial RuO2. Moreover, the NiFe-oxyhydroxide also exhibits remarkable activity towards hydrogen evolution reaction by demanding a minimal overpotential of 118 mV that is relatively lower than the commercial Pt/C to obtain a current density of 10 mA cm−2. With the implication of prepared Ni(OH)2NiOOH/FeOOH both as anode and cathode, the fabricated electrolyzer demonstrates a minimal cell voltage of 1.52 V to attain a current density of 10 mA cm−2 and displays an extended stability for a period of 50 h.
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