{"title":"F‐Mediated Precise Control Over Amorphous/Crystalline Fe/Ni‐Based Phosphides Heterostructure for Efficient Oxygen Evolution Reaction","authors":"Hui Li, Xin Li, Qilin Gu, Shiyou Zheng","doi":"10.1002/rar2.70084","DOIUrl":null,"url":null,"abstract":"ABSTRACT Transition metal‐based amorphous/crystalline (a/c) heterostructured catalysts have garnered significant attention due to their exceptional activity, stability, and cost‐effectiveness. However, the precise synergistic regulation of interfacial composition and phase states remains challenging. Herein, we propose an innovative strategy for the controllable synthesis of a/c heterostructures using MIL‐100(Mn) template. By leveraging the intrinsic coordination disparity between Ni 2+ and Fe 3+ to drive phase separation, combined with F − mediated ion exchange‐phosphidation synergy, we successfully constructed an amorphous FeP x /crystalline Ni 2 P heterostructure (a‐(F, Fe)P x /Ni 2 P) with precise compositional control. Systematic investigations reveal that F − not only enhances metal ion exchange through complex stabilization but also induces amorphous/crystalline phase separation via electronic modulation. Meanwhile, a deep reconstruction process occurs under high voltage, transforming the catalyst into active F‐Fe/NiOOH species, which further enhances the catalytic activity and durability. Benefiting from the synergistic effects of heterointerface electronic coupling and deep reconstruction, the as‐prepared a‐(F, Fe)P x /Ni 2 P catalyst exhibits exceptional oxygen evolution reaction (OER) performance in 1 M KOH, delivering an ultralow overpotential of 278 mV at 30 mA cm −2 and maintaining excellent stability over 100 h with negligible degradation. This work establishes a novel “coordination difference‐driven, fluorine‐mediated” interface engineering strategy, offering valuable insights for the rational design of high‐performance heterostructured electrocatalysts.","PeriodicalId":749,"journal":{"name":"Rare Metals","volume":"45 2","pages":""},"PeriodicalIF":12.1000,"publicationDate":"2025-12-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/rar2.70084","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare Metals","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.1002/rar2.70084","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
ABSTRACT Transition metal‐based amorphous/crystalline (a/c) heterostructured catalysts have garnered significant attention due to their exceptional activity, stability, and cost‐effectiveness. However, the precise synergistic regulation of interfacial composition and phase states remains challenging. Herein, we propose an innovative strategy for the controllable synthesis of a/c heterostructures using MIL‐100(Mn) template. By leveraging the intrinsic coordination disparity between Ni 2+ and Fe 3+ to drive phase separation, combined with F − mediated ion exchange‐phosphidation synergy, we successfully constructed an amorphous FeP x /crystalline Ni 2 P heterostructure (a‐(F, Fe)P x /Ni 2 P) with precise compositional control. Systematic investigations reveal that F − not only enhances metal ion exchange through complex stabilization but also induces amorphous/crystalline phase separation via electronic modulation. Meanwhile, a deep reconstruction process occurs under high voltage, transforming the catalyst into active F‐Fe/NiOOH species, which further enhances the catalytic activity and durability. Benefiting from the synergistic effects of heterointerface electronic coupling and deep reconstruction, the as‐prepared a‐(F, Fe)P x /Ni 2 P catalyst exhibits exceptional oxygen evolution reaction (OER) performance in 1 M KOH, delivering an ultralow overpotential of 278 mV at 30 mA cm −2 and maintaining excellent stability over 100 h with negligible degradation. This work establishes a novel “coordination difference‐driven, fluorine‐mediated” interface engineering strategy, offering valuable insights for the rational design of high‐performance heterostructured electrocatalysts.
过渡金属基非晶/晶体(a/c)异质结构催化剂因其优异的活性、稳定性和成本效益而受到广泛关注。然而,界面组成和相态的精确协同调节仍然具有挑战性。在此,我们提出了一种利用MIL‐100(Mn)模板可控合成a/c异质结构的创新策略。通过利用Ni 2+和fe3 +之间的内在配位差来驱动相分离,结合F−介导的离子交换-磷化协同作用,我们成功构建了非晶FeP x /晶体ni2p异质结构(a‐(F, Fe)P x / ni2p),并精确控制了成分。系统研究表明,F−不仅通过络合物稳定增强金属离子交换,而且通过电子调制诱导非晶/晶体相分离。同时,在高压下发生深度重构过程,将催化剂转化为活性的F - Fe/NiOOH,进一步提高了催化活性和耐久性。得益于异质界面电子耦合和深度重构的协同效应,制备的a - (F, Fe)P x /Ni 2 P催化剂在1 M KOH下表现出优异的析氧反应(OER)性能,在30 mA cm - 2下提供278 mV的超低过电位,并在100小时内保持优异的稳定性,降解几乎可以忽略不计。这项工作建立了一种新的“配位差异驱动,氟介导”的界面工程策略,为高性能异质结构电催化剂的合理设计提供了有价值的见解。
期刊介绍:
Rare Metals is a monthly peer-reviewed journal published by the Nonferrous Metals Society of China. It serves as a platform for engineers and scientists to communicate and disseminate original research articles in the field of rare metals. The journal focuses on a wide range of topics including metallurgy, processing, and determination of rare metals. Additionally, it showcases the application of rare metals in advanced materials such as superconductors, semiconductors, composites, and ceramics.