在RuO2中通过Cr/Mo共掺杂构建晶态-非晶态异相界面,实现了高效的酸性析氧反应

IF 2.6 4区 化学 Q3 CHEMISTRY, PHYSICAL
Ionics Pub Date : 2025-07-07 DOI:10.1007/s11581-025-06485-w
Jian Yang, Yaowen Zhang, Yongping Liu
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引用次数: 0

摘要

析氧反应(OER)作为电解水的阳极,在各种应用中起着举足轻重的作用。开发高效的非铱基酸性水裂解催化剂仍然是一个重大挑战。本研究采用相工程策略,通过双金属掺杂合成了富缺陷结晶/非晶态Ru0.6Mo0.2Cr0.2Ox固溶体催化剂。该催化剂表现出优异的酸性OER性能,过电位为204 mV (@10 mA cm−2),在1.5 V vs RHE下的质量活性为577.8 A gRu−1,优于所有对照样品。此外,协同Cr/Mo掺杂有效地降低了Ru在RuO2中的氧化态,同时增强了结构稳定性,从而在长时间的测试中使活性衰减最小。理论计算表明,双掺杂协同调节了Ru位点上的电荷分布,降低了热力学限制步骤中*OOH形成的能垒。这项工作为开发具有显著减少贵金属负载的高性能酸性OER催化剂提供了一个简单的策略,展示了关键的工业相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Constructing crystalline-amorphous heterophase interfaces through Cr/Mo co-doping in RuO2 enables efficient acidic oxygen evolution reaction

The oxygen evolution reaction (OER), serving as the anode in water electrolysis, plays a pivotal role in various applications. Developing efficient non-iridium-based catalysts for acidic water splitting remains a significant challenge. This study employs a phase engineering strategy to synthesize defect-rich crystalline/amorphous Ru0.6Mo0.2Cr0.2Ox solid solution catalysts through dual-metal doping. The catalyst exhibits superior acidic OER performance with an overpotential of 204 mV (@10 mA cm−2) and mass activity of 577.8 A gRu−1 at 1.5 V vs RHE, outperforming all control samples. Furthermore, synergistic Cr/Mo doping effectively reduces the oxidation state of Ru in RuO2 while enhancing structural stability, resulting in minimal activity decay during prolonged testing. Theoretical calculations reveal that dual-doping synergistically modulates charge distribution on Ru sites, lowering the energy barrier for *OOH formation in the thermodynamic limiting step. This work provides a facile strategy for developing high-performance acidic OER catalysts with dramatically reduced noble metal loading, demonstrating critical industrial relevance.

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来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
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