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负载在泡沫镍上的硫掺杂FeO纳米片阵列用于高效碱性海水分解。

Sulfur doped FeO nanosheet arrays supported on nickel foam for efficient alkaline seawater splitting.

作者信息

Hao Weiju, Fan Jinli, Xu Xia, Zhang Yiran, Lv Haiyang, Wang Shige, Deng Shengwei, Weng Shuo, Guo Yanhui

机构信息

University of Shanghai for Science and Technology, Shanghai, 200093, China.

College of Chemical Engineering, Zhejiang University of Technology, Hangzhou, 310014, China.

出版信息

Dalton Trans. 2021 Oct 5;50(38):13312-13319. doi: 10.1039/d1dt02506f.

Abstract

Developing economical, efficient and stable bifunctional catalysts for hydrogen production from seawater is of great significance for hydrogen utilization. Herein, sulfur doped iron oxide nanosheet arrays supported on nickel foam (FeO-NiS@NF) are prepared by a one-pot solvothermal reaction. Owing to the high intrinsic activity of FeO-NiS, the large catalytic specific surface area of nanosheet arrays and the fast charge transportation capability achieved by the self-supporting configuration, the FeO-NiS@NF electrode delivers excellent catalytic performance in alkaline simulated seawater (1 M KOH + 0.5 M NaCl). Impressively, a low overpotential of 120 mV at 50 mA cm with a Tafel slope of 57 mV dec for the hydrogen evolution reaction and an overpotential of 470 mV at 200 mA cm with a Tafel slope of 62 mV dec for the oxygen evolution reaction are achieved. More importantly, the voltage is only 1.5 V at 50 mA cm for continuous overall water splitting for 100 h at 200 mA cm with negligible decay in alkaline simulated seawater with almost 100% Faraday efficiency. This work provides a simple and universal strategy to prepare highly efficient bifunctional catalytic materials, promoting the development of Earth-abundant materials to catalyse seawater splitting to produce high-purity hydrogen.

摘要

开发经济、高效且稳定的用于海水制氢的双功能催化剂对氢能利用具有重要意义。在此,通过一锅法溶剂热反应制备了负载在泡沫镍上的硫掺杂氧化铁纳米片阵列(FeO-NiS@NF)。由于FeO-NiS的高本征活性、纳米片阵列的大催化比表面积以及自支撑结构实现的快速电荷传输能力,FeO-NiS@NF电极在碱性模拟海水(1 M KOH + 0.5 M NaCl)中表现出优异的催化性能。令人印象深刻的是,析氢反应在50 mA cm时的低过电位为120 mV,塔菲尔斜率为57 mV dec,析氧反应在200 mA cm时的过电位为470 mV,塔菲尔斜率为62 mV dec。更重要的是,在碱性模拟海水中,200 mA cm下连续全水解100 h,50 mA cm时电压仅为1.5 V,衰减可忽略不计,法拉第效率几乎为100%。这项工作提供了一种简单通用的策略来制备高效双功能催化材料,推动了用地球上储量丰富的材料催化海水分解以生产高纯度氢气的发展。

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