Runxu Deng, Feng Liu*, Shixin Gao, Zhenwei Xia, Runjie Wu, Jincheng Kong, Jin Yang, Jiahao Wen, Xiao Zhang, Chade Lv, Yuhao Wang, Xiaoguang Li and Zheng Wang*,
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Here, we combine density functional theory (DFT) calculations with experimental validation to enhance the activity and stability of β-MnO<sub>2</sub> via co-substitution with ruthenium (Ru) and iridium (Ir), enabling the transition from AEM to OPM. DFT calculations reveal that AEM is hindered by the weak nucleophilicity of water, while LOM suffers from high kinetic barriers due to structural distortions. In contrast, OPM demonstrates a significantly lower kinetic barrier, facilitated by the synergistic interaction between Ru and Ir. Experimentally, IrRuMnO<sub><i>x</i></sub> was synthesized through co-precipitation and hydrothermal methods, showing an 80-fold improvement in mass activity and a 96-fold increase in stability compared to commercial IrO<sub>2</sub>, with minimal noble metal leaching, as confirmed by inductively coupled plasma optical emission spectroscopy (ICP-OES). IrRuMnO<sub><i>x</i></sub> exhibited an ultralow overpotential of 475 mV at 1 A·cm<sup>–2</sup> and a Tafel slope of 44.26 mV·dec<sup>–1</sup> in 0.5 M H<sub>2</sub>SO<sub>4</sub>, maintaining stable performance for over 100 h. Moreover, the IrRuMnO<sub><i>x</i></sub>-based membrane electrode, with a low Ir loading of 0.075 mg<sub>Ir</sub>·cm<sup>–2</sup>, achieved remarkable current densities of 1.0 A·cm<sup>–2</sup> at 1.66 V and 2.0 A·cm<sup>–2</sup> at 1.91 V at 80 °C. This performance surpasses that of both unsupported and conventional supported Ir-based catalysts at comparable Ir loading levels. This study offers critical insights into OER mechanisms in acidic media and paves the way for developing efficient and durable OER electrocatalysts for hydrogen production.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"15 3","pages":"1782–1794 1782–1794"},"PeriodicalIF":13.1000,"publicationDate":"2025-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rational Design of β-MnO2 via Ir/Ru Co-substitution for Enhanced Oxygen Evolution Reaction in Acidic Media\",\"authors\":\"Runxu Deng, Feng Liu*, Shixin Gao, Zhenwei Xia, Runjie Wu, Jincheng Kong, Jin Yang, Jiahao Wen, Xiao Zhang, Chade Lv, Yuhao Wang, Xiaoguang Li and Zheng Wang*, \",\"doi\":\"10.1021/acscatal.4c0598910.1021/acscatal.4c05989\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The efficiency of the oxygen evolution reaction (OER) in acidic media is severely limited by the poor stability, low activity, and high cost of available catalysts. 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Experimentally, IrRuMnO<sub><i>x</i></sub> was synthesized through co-precipitation and hydrothermal methods, showing an 80-fold improvement in mass activity and a 96-fold increase in stability compared to commercial IrO<sub>2</sub>, with minimal noble metal leaching, as confirmed by inductively coupled plasma optical emission spectroscopy (ICP-OES). IrRuMnO<sub><i>x</i></sub> exhibited an ultralow overpotential of 475 mV at 1 A·cm<sup>–2</sup> and a Tafel slope of 44.26 mV·dec<sup>–1</sup> in 0.5 M H<sub>2</sub>SO<sub>4</sub>, maintaining stable performance for over 100 h. Moreover, the IrRuMnO<sub><i>x</i></sub>-based membrane electrode, with a low Ir loading of 0.075 mg<sub>Ir</sub>·cm<sup>–2</sup>, achieved remarkable current densities of 1.0 A·cm<sup>–2</sup> at 1.66 V and 2.0 A·cm<sup>–2</sup> at 1.91 V at 80 °C. This performance surpasses that of both unsupported and conventional supported Ir-based catalysts at comparable Ir loading levels. 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引用次数: 0
摘要
酸性介质中析氧反应(OER)的效率受到现有催化剂稳定性差、活性低和成本高的严重限制。在保持稳定和减少对贵金属依赖的同时,加强内在活动至关重要。典型的吸附质演化机制(AEM)导致高过电位和低活性,使过渡到替代机制,如晶格氧机制(LOM)或氧化物路径机制(OPM),由于它们的低过电位而非常理想。本文将密度泛函理论(DFT)计算与实验验证相结合,通过与钌(Ru)和铱(Ir)共取代,提高β-MnO2的活性和稳定性,实现从AEM到OPM的转变。DFT计算表明,AEM受到水的弱亲核性的阻碍,而LOM由于结构畸变而受到高动力学障碍的影响。相比之下,由于Ru和Ir之间的协同作用,OPM表现出明显较低的动力学势垒。实验中,通过共沉淀法和水热法合成了IrRuMnOx,与商用IrO2相比,其质量活性提高了80倍,稳定性提高了96倍,并且电感耦合等离子体光学发射光谱(ICP-OES)证实了贵金属浸出最少。在0.5 M H2SO4中,IrRuMnOx的过电位为475 mV,过电位为44.26 mV·dec1,在100 h以上的时间内保持稳定。此外,IrRuMnOx基膜电极在0.075 mgIr·cm-2的低Ir负载下,在1.66 V时电流密度为1.0 A·cm-2,在80°C时电流密度为2.0 A·cm-2。在相当的Ir负载水平下,这种性能超过了无负载和传统负载的Ir基催化剂。这项研究为酸性介质中的OER机制提供了重要的见解,并为开发高效耐用的OER制氢电催化剂铺平了道路。
Rational Design of β-MnO2 via Ir/Ru Co-substitution for Enhanced Oxygen Evolution Reaction in Acidic Media
The efficiency of the oxygen evolution reaction (OER) in acidic media is severely limited by the poor stability, low activity, and high cost of available catalysts. Enhancing intrinsic activity while maintaining stability and reducing reliance on precious metals is crucial. The typical adsorbate evolution mechanism (AEM) leads to high overpotentials and low activity, making the transition to alternative mechanisms, such as the lattice oxygen mechanism (LOM) or oxide path mechanism (OPM), highly desirable due to their lower overpotentials. Here, we combine density functional theory (DFT) calculations with experimental validation to enhance the activity and stability of β-MnO2 via co-substitution with ruthenium (Ru) and iridium (Ir), enabling the transition from AEM to OPM. DFT calculations reveal that AEM is hindered by the weak nucleophilicity of water, while LOM suffers from high kinetic barriers due to structural distortions. In contrast, OPM demonstrates a significantly lower kinetic barrier, facilitated by the synergistic interaction between Ru and Ir. Experimentally, IrRuMnOx was synthesized through co-precipitation and hydrothermal methods, showing an 80-fold improvement in mass activity and a 96-fold increase in stability compared to commercial IrO2, with minimal noble metal leaching, as confirmed by inductively coupled plasma optical emission spectroscopy (ICP-OES). IrRuMnOx exhibited an ultralow overpotential of 475 mV at 1 A·cm–2 and a Tafel slope of 44.26 mV·dec–1 in 0.5 M H2SO4, maintaining stable performance for over 100 h. Moreover, the IrRuMnOx-based membrane electrode, with a low Ir loading of 0.075 mgIr·cm–2, achieved remarkable current densities of 1.0 A·cm–2 at 1.66 V and 2.0 A·cm–2 at 1.91 V at 80 °C. This performance surpasses that of both unsupported and conventional supported Ir-based catalysts at comparable Ir loading levels. This study offers critical insights into OER mechanisms in acidic media and paves the way for developing efficient and durable OER electrocatalysts for hydrogen production.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.