Amorphous–crystalline FeNi2S4@NiFe–LDH nanograsses with molten salt as an industrially promising electrocatalyst for oxygen evolution†

IF 6.2 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Fu-Li Wang, Xin- Yu Zhang, Jian-Cheng Zhou, Zhuo-Ning Shi, Bin Dong, Jing-Yi Xie, Yi-Wen Dong, Jian-Feng Yu and Yong-Ming Chai
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引用次数: 9

Abstract

Inexpensive and accessible NiFe-based oxygen evolution reaction (OER) electrocatalysts show limitations for practical industrial applications owing to their activity and stability under industrial conditions. Herein, an FeNi2S4@NiFe–LDH heterostructure is constructed by the molten salt method and interfacial corrosion strategy, in which amorphous NiFe–LDH nanosheets grow in situ on the surface of crystalline FeNi2S4 with a nanograss structure. The introduction of amorphous NiFe–LDH can not only optimize the adsorption energy of OER intermediates, but also significantly improve the overall stability and activity of the catalyst by reducing the loss of the S element in FeNi2S4. At the same time, the OH? produced by S ion hydrolysis can also promote the in situ construction of NiFe–LDH. Such an amorphous–crystalline structure gives full contribution to the advantages of each component, modulates the nanostructure, and promotes the electron transfer across the interfaces. Consequently, FeNi2S4@NiFe–LDH achieves large current density values of 500 and 1000 mA cm?2 for the OER at overpotentials of only 283 and 306 mV in 1 M KOH (25 °C) without losing performance for at least 600 h at 500 mA cm?2. Under the simulated practical industrial test conditions (6 M KOH, 70 °C), the same current densities of 500 and 1000 mA cm?2 are delivered at the ultra-low overpotentials of 137 and 155 mV with long-term stability at high and low current densities. Such excellent catalyst performance shows its great industrial application prospects. This work also provides a strategy using Earth-abundant materials for realizing large-scale water splitting.

Abstract Image

无定形结晶FeNi2S4@NiFe -LDH纳米草与熔盐作为工业上有前途的析氧电催化剂†
廉价和易于获得的nife基析氧反应(OER)电催化剂由于其在工业条件下的活性和稳定性而受到实际工业应用的限制。本文采用熔盐法和界面腐蚀策略构建了FeNi2S4@NiFe -LDH异质结构,在具有纳米草结构的晶体FeNi2S4表面原位生长了非晶NiFe-LDH纳米片。无定形NiFe-LDH的引入不仅可以优化OER中间体的吸附能,还可以通过减少FeNi2S4中S元素的损失,显著提高催化剂的整体稳定性和活性。同时,OH?S离子水解产生的产物也能促进NiFe-LDH的原位构建。这种非晶结构充分发挥了各组分的优势,调节了纳米结构,促进了电子在界面上的传递。因此,FeNi2S4@NiFe -LDH实现了500和1000 mA cm?在1 M KOH(25°C)下,过电位仅为283和306 mV时的OER在500 mA cm下不损失性能至少600小时。在模拟的实际工业测试条件下(6 M KOH, 70°C),相同的电流密度为500和1000 mA cm?2在137和155 mV的超低过电位下交付,在高电流密度和低电流密度下具有长期稳定性。如此优异的催化剂性能显示出其巨大的工业应用前景。这项工作也提供了利用地球上丰富的材料实现大规模水分解的策略。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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