电解
海水
溶解
过电位
氯
催化作用
腐蚀
阳极
吸附
析氧
金属
电解水
离子交换
材料科学
质子交换膜燃料电池
水溶液中的金属离子
无机化学
化学
氯化物
钝化
化学工程
厌氧腐蚀
制氢
氢
分解水
润湿
电化学
电催化剂
电流密度
法拉第效率
过氧化氢
人工海水
双功能催化剂
作者
Peng Wang,Jie Zheng,Yuyang Li,Qiaofu Shi,Jun Zhang,Yong Wan,Mang Niu,Yusuke Yamauchi,Yun‐Ze Long
标识
DOI:10.1002/advs.202514301
摘要
Alkaline seawater electrolysis is a promising technology for sustainable green hydrogen production. However, active metal dissolution and chlorine-induced corrosion during long-term, industrial-scale operation pose critical challenges to catalyst stability. Here, a surface engineering strategy is reported using phytic acid (PA) as a molecular "armor" to construct highly durable oxygen evolution reaction (OER) catalysts. Comprehensive characterization and density functional theory (DFT) calculations reveal that surface modification with PO4 3- groups not only facilitates surface reconstruction to form NiOOH active sites, but also optimizes the adsorption-desorption dynamics of key reaction intermediates, thereby enhancing catalytic performance. Importantly, the PO4 3- layer suppresses the adsorption of chloride ions at active sites, significantly improving corrosion resistance under harsh seawater conditions. As a result, the catalyst delivers a current density of 100 mA cm-2 at a low overpotential of 208 mV in alkaline seawater, maintaining stable performance over 1500 h. When integrated as the anode in a proton exchange membrane electrolyzer, it supports operation at 1 A cm-2 with a cell voltage of only 2.18 V, exhibiting no performance degradation over 500 h.
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