Yao Dai, Xueyang Tu, Kaihang Yue, Yingjie Wan, Peng Zhao, Xuerong Shi, Fuqiang Huang, Ya Yan
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引用次数: 0
Abstract
Direct seawater electrolysis is a promising technology for massive green hydrogen production but is limited by the lack of durable and efficient electrocatalysts toward the oxygen evolution reaction (OER). Herein, a high entropy phosphorus sulfide (HEPS) is prepared as a high-performance OER catalyst for seawater splitting through a simple vacuum high-temperature sintering method. This catalyst needs overpotentials of merely 245 and 313 mV in alkalized seawater to deliver current densities of 10 and 100 mA cm−2, respectively, and operates continuously for 1200 h in a practical electrolyzer with negligible activity decay, making it one of the best OER catalysts for seawater electrolysis reported to date. Detailed experimental and theoretical analyses reveal that the excellent durability of HEPS originates from the P and S in the material is oxidized and forms an anionic protective layer to repel chloride ions, preventing further corrosion of the material. Meanwhile, the formed V2Ox species can effectively prevent the material from further oxidation. Further, a highly stable and efficient seawater electrolyzer is assembled with the HEPS anode and the Ru@C cathode to demonstrate the practicability of the catalysts.
海水直接电解是一种很有前途的大规模绿色制氢技术,但由于缺乏耐用和高效的析氧反应电催化剂而受到限制。本文采用简单的真空高温烧结方法制备了高熵硫化磷(HEPS)作为海水裂解的高性能OER催化剂。该催化剂在碱化海水中的过电位仅为245 mV和313 mV,电流密度分别为10和100 mA cm - 2,并且在实际电解槽中连续工作1200 h,活性衰减可以忽略不计,是迄今为止报道的最好的海水电解OER催化剂之一。详细的实验和理论分析表明,HEPS优异的耐久性源于材料中的P和S被氧化,形成阴离子保护层,排斥氯离子,防止材料进一步腐蚀。同时,形成的vox物质能有效防止材料进一步氧化。此外,采用HEPS阳极和Ru@C阴极组装了一个高度稳定和高效的海水电解槽,以证明催化剂的实用性。
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