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作为用于海水电解的高电催化选择性析氧反应电极的异质镍铁硫化物的界面构型

Interfacial configuration of heterogeneous NiFe-sulfide as a highly electrocatalytic selective oxygen evolution reaction electrode toward seawater electrolysis.

作者信息

Yang Yang, Zhang Shengzhong, Song Zhaoyang, Wang Hongtao, Zhang Yanpeng, Fan Dequan, Hu Fangzhou, Yu Ying, Zhang Ying

机构信息

Sinopec Dalian Research Institute of Petroleum and Petrochemicals Dalian 116045 Liaoning P. R. China

出版信息

RSC Adv. 2022 Oct 7;12(44):28623-28628. doi: 10.1039/d2ra04253c. eCollection 2022 Oct 4.

Abstract

Seawater electrolysis for scalable hydrogen generation has attracted much attention due to the abundance of seawater in nature. However, it is severely impeded by the chlorine ions in seawater, which can cause corrosion and an undesirable competing reaction at the anode. So it is highly desirable to exploit a highly active, chlorine corrosion resistant and selective OER electrode for seawater splitting. Here, a heterogeneous NiFe-sulfide electrode is proposed to achieve an efficient OER process in alkaline seawater. Considering the 2D lamellar architecture with a rough surface and a considerable amount of micro voids, the dual electronic configuration of sulfur and iron, the strong synergistic effect between Ni and Fe at the atomic level and the interfacial engineering between the NiS/NiS phase and FeS phase at the nanoscale level, the NiFeS-0.05 M electrode exhibits predominant catalytic activity with an overpotential of 353 mV to reach 200 mA cm, superior long-term stability with 50 h accelerated stability test and higher selectivity toward the OER.

摘要

由于自然界中海水资源丰富,用于大规模制氢的海水电解备受关注。然而,海水中的氯离子严重阻碍了这一过程,氯离子会导致腐蚀并在阳极引发不良的竞争反应。因此,开发一种高活性、耐氯腐蚀且具有选择性的析氧反应(OER)电极用于海水分解非常必要。在此,提出了一种异质NiFe硫化物电极,以在碱性海水中实现高效的析氧反应过程。考虑到具有粗糙表面和大量微孔的二维层状结构、硫和铁的双电子构型、镍和铁在原子水平上的强协同效应以及纳米级镍硫化物/镍硫化物相和硫化铁相之间的界面工程,NiFeS-0.05 M电极表现出卓越的催化活性,过电位为353 mV时达到200 mA cm,在50小时加速稳定性测试中具有优异的长期稳定性,并且对析氧反应具有更高的选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d727/9539616/c6f5024b9ca9/d2ra04253c-f1.jpg

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