Recent advances in lanthanide-based materials for oxygen evolution reaction: Challenges and future prospects

IF 23.5 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Coordination Chemistry Reviews Pub Date : 2025-03-04 DOI:10.1016/j.ccr.2025.216573
Sheraz Muhammad , Lixia Wang , Zhiyang Huang , Aling Zhou , Hazrat Bilal , Tayirjan Taylor Isimjan , Xiulin Yang
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Abstract

Lanthanide-based materials have emerged as highly promising electrocatalysts for the oxygen evolution reaction (OER), a pivotal process in water splitting and energy conversion applications. These materials present a sustainable and cost-effective alternative to noble-metal catalysts, addressing critical challenges of scarcity and cost. Their exceptional catalytic activity and stability are attributed to unique electronic properties, including multiple oxidation states, large ionic radius, and strong spin-orbit coupling. Recent breakthroughs demonstrate significant enhancements in overpotential reduction and long-term stability under extreme electrochemical conditions, positioning lanthanides as a transformative solution for renewable energy systems. This review comprehensively explores various classes of lanthanide-based OER electrocatalysts, including transition metals, metal-organic frameworks (MOFs), perovskites, nanomaterials, and chalcogenides, nitrides, borides, and phosphides. Perovskites, in particular, have achieved remarkable stability and efficiency, underscoring their potential for real-world applications. Tailored strategies such as anionic substitution and heteroatom doping further optimize the electronic structure, active site stabilization, and charge transfer efficiency, driving significant performance improvements. Notably, recent studies report a substantial reduction in overpotential by up to 200 mV for lanthanide-based materials, along with significantly enhanced catalytic durability compared to conventional noble-metal catalysts. Key challenges remain, such as improving electrical conductivity, scalability, and performance longevity. Strategic integration of lanthanides into catalytic frameworks addresses these limitations while reducing reliance on scarce resources. These advancements enable lanthanide-based OER electrocatalysts to revolutionize renewable energy technologies and drive the commercialization of efficient water-splitting and electrochemical processes.

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稀土系析氧材料的研究进展:挑战与展望
镧系材料已成为极有前途的析氧反应(OER)电催化剂,是水分解和能量转换应用的关键过程。这些材料为贵金属催化剂提供了一种可持续且具有成本效益的替代品,解决了稀缺和成本的关键挑战。其优异的催化活性和稳定性归功于其独特的电子性质,包括多种氧化态、大离子半径和强自旋轨道耦合。最近的突破表明,在极端电化学条件下,镧系元素在过电位降低和长期稳定性方面有了显著的增强,将其定位为可再生能源系统的变革性解决方案。本文综述了各类镧系OER电催化剂,包括过渡金属、金属有机框架(mof)、钙钛矿、纳米材料、硫族化合物、氮化物、硼化物和磷化物。特别是钙钛矿,已经取得了显著的稳定性和效率,强调了它们在实际应用中的潜力。阴离子取代和杂原子掺杂等定制策略进一步优化了电子结构、活性位点稳定和电荷转移效率,从而显著提高了性能。值得注意的是,最近的研究报告称,与传统的贵金属催化剂相比,镧系材料的过电位大幅降低了200 mV,同时显著提高了催化耐久性。关键的挑战仍然存在,比如提高导电性、可扩展性和性能寿命。将镧系元素战略性地纳入催化框架解决了这些限制,同时减少了对稀缺资源的依赖。这些进步使镧系OER电催化剂能够彻底改变可再生能源技术,并推动高效水分解和电化学过程的商业化。
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来源期刊
Coordination Chemistry Reviews
Coordination Chemistry Reviews 化学-无机化学与核化学
CiteScore
34.30
自引率
5.30%
发文量
457
审稿时长
54 days
期刊介绍: Coordination Chemistry Reviews offers rapid publication of review articles on current and significant topics in coordination chemistry, encompassing organometallic, supramolecular, theoretical, and bioinorganic chemistry. It also covers catalysis, materials chemistry, and metal-organic frameworks from a coordination chemistry perspective. Reviews summarize recent developments or discuss specific techniques, welcoming contributions from both established and emerging researchers. The journal releases special issues on timely subjects, including those featuring contributions from specific regions or conferences. Occasional full-length book articles are also featured. Additionally, special volumes cover annual reviews of main group chemistry, transition metal group chemistry, and organometallic chemistry. These comprehensive reviews are vital resources for those engaged in coordination chemistry, further establishing Coordination Chemistry Reviews as a hub for insightful surveys in inorganic and physical inorganic chemistry.
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