{"title":"Oxophilic Sites Mediated Dynamic Oxygen Replenishment to Stabilize Lattice Oxygen Catalysis in Acidic Water Oxidation","authors":"Shaoxiong Li, Sheng Zhao, Sung-Fu Hung, Liming Deng, Luqi Wang, Fuke Shi, Ao Dong, Ying Zhang, Tsung-Yi Chen, Feng Hu, Linlin Li, Seeram Ramakrishna, Yuping Wu and Shengjie Peng*, ","doi":"10.1021/jacs.5c09939","DOIUrl":null,"url":null,"abstract":"<p >Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O<sub>L</sub>) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O<sub>L</sub> actively participates in O–O bond formation and is continuously refilled by water-derived species. Oxophilic dopants modulate the local electronic structure, lower the energy barrier for oxygen vacancy healing, and reorganize the interfacial hydrogen-bond network to enhance water mobility, orientation, and proton accessibility, collectively promoting water dissociation and stabilizing O<sub>L</sub> catalysis. The optimized catalyst achieves a low overpotential of 289 mV and exceptional durability, operating continuously for 650 h at 10 mA cm<sup>–2</sup> in acidic electrolyte and maintaining stable performance for 280 h at 1 A cm<sup>–2</sup> in a PEMWE. This work establishes a mechanistic framework for dynamic O<sub>L</sub> redox and provides a rational strategy for designing robust, noble-metal-free acidic OER electrocatalysts.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":"147 37","pages":"33770–33779"},"PeriodicalIF":15.6000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/jacs.5c09939","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (OL) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which OL actively participates in O–O bond formation and is continuously refilled by water-derived species. Oxophilic dopants modulate the local electronic structure, lower the energy barrier for oxygen vacancy healing, and reorganize the interfacial hydrogen-bond network to enhance water mobility, orientation, and proton accessibility, collectively promoting water dissociation and stabilizing OL catalysis. The optimized catalyst achieves a low overpotential of 289 mV and exceptional durability, operating continuously for 650 h at 10 mA cm–2 in acidic electrolyte and maintaining stable performance for 280 h at 1 A cm–2 in a PEMWE. This work establishes a mechanistic framework for dynamic OL redox and provides a rational strategy for designing robust, noble-metal-free acidic OER electrocatalysts.
开发高效、耐用的酸性介质析氧反应催化剂是推进质子交换膜电解(PEMWE)的必要条件。然而,晶格氧(OL)耗竭和金属溶解引起的催化剂不稳定性仍然是一个关键障碍。在此,我们提出了一种亲氧位点介导的动态氧补充机制(DORM),其中OL积极参与O-O键的形成,并不断被水源物种补充。亲氧掺杂剂调节局部电子结构,降低氧空位愈合的能垒,重组界面氢键网络,增强水的迁移率、取向和质子可及性,共同促进水解离和稳定OL催化。优化后的催化剂实现了289 mV的低过电位和优异的耐久性,在酸性电解质中以10 mA cm-2连续工作650小时,并在PEMWE中以1 a cm-2保持280小时的稳定性能。这项工作建立了OL动态氧化还原的机制框架,并为设计坚固的、无贵金属的酸性OER电催化剂提供了合理的策略。
期刊介绍:
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