Dual-metal hydroxide@oxide heterojunction catalyst constructed via corrosion engineering for large-current oxygen evolution reaction
Current OER electrocatalysts are hardly applicable for industrial use, which demands high current density (≥ 1000 mA cm-2) at low overpotential (≤ 300 mV) with long-term stability (≥ 100 h). Herein self-supported heterojunction catalyst, NiCo-OH@NixFeyO4 on Fe foam (FF), is in situ synthesized using...
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المؤلفون الرئيسيون: | , , , , , |
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مؤلفون آخرون: | |
التنسيق: | مقال |
اللغة: | English |
منشور في: |
2023
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الموضوعات: | |
الوصول للمادة أونلاين: | https://hdl.handle.net/10356/169002 |
الوسوم: |
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الملخص: | Current OER electrocatalysts are hardly applicable for industrial use, which demands high current density (≥ 1000 mA cm-2) at low overpotential (≤ 300 mV) with long-term stability (≥ 100 h). Herein self-supported heterojunction catalyst, NiCo-OH@NixFeyO4 on Fe foam (FF), is in situ synthesized using two-step corrosion engineering. It only requires an overpotential 275 mV to drive the current density of 1000 mA cm-2 with good long-term stability. Theoretical calculations reveal that such good performance is attributable to electron transfer from NiCo-OH to NixFeyO4 which weakens the adsorption energy of reaction intermediate (OOH*) to promote the release of O2 and lowers the free energy barriers for the reaction. Furthermore, a water splitting cell with NiCo-OH@NixFeyO4/FF as anode and CoP@FeP/FF as cathode demonstrates its potential for industrial application. The study presents a general strategy for in situ synthesis of heterojunction catalysts on metal foams using controlled corrosion engineering for various catalytic applications. |
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