Li Yao, jun guo, Chaoxin Yang, Zixiao Li, Shengjun Sun, Yue Meng, Wei Zuo, Xixi Zhang, Hefeng Wang, Fatma A. Ibrahim, Mohamed S. Hamdy, Wenbo Lu, Xuping Sun, Bo Tang
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引用次数: 0
Abstract
Seawater electrolysis is a promising method for producing hydrogen, but the generation of corrosive chlorine species (e.g., chloride and hypochlorite) remains a critical challenge. Herein, we successfully synthesized a FeNiP/MoOx/NiMoO4/NF electrocatalyst through Fe doping and subsequent phosphidation of NiMoO4/NF, which exhibits exceptional activity and stability for alkaline seawater oxidation. FeNiP/MoOx/NiMoO4/NF requires an overpotential of 349 mV to reach a current density (j) of 1000 mA cm−2, showing constant operation for 500 h at the same j. Furthermore, an anion-exchange membrane electrolyzer equipped with FeNiP/MoOx/NiMoO4/NF demonstrates excellent performance, requiring only 2.12 V to achieve 300 mA cm−2 while maintaining stable operation for 180 h.
海水电解是一种很有前途的制氢方法,但产生腐蚀性氯(如氯化物和次氯酸盐)仍然是一个关键的挑战。本文通过Fe掺杂和NiMoO4/NF的后续磷化,成功合成了FeNiP/MoOx/NiMoO4/NF电催化剂,该催化剂对碱性海水氧化具有优异的活性和稳定性。FeNiP/MoOx/NiMoO4/NF需要349 mV的过电位才能达到1000 mA cm−2的电流密度(j),在相同的电流密度下可连续工作500 h。此外,配备FeNiP/MoOx/NiMoO4/NF的阴离子交换膜电解槽表现出优异的性能,仅需2.12 V即可达到300 mA cm−2,并保持180 h的稳定运行。
期刊介绍:
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