ArticleNature materials2026
Synthesis of 4H-phase high-entropy alloys for electrocatalysis.
Article in Nature materials, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
3 citing papers in PubMed.
- Buffering the Active State for Proton Exchange Membrane Water Electrolysis.Angewandte Chemie (International ed. in English) · 2026Review
- Electrocatalysis and Photoelectrocatalysis: Perspective from Physicochemical Mechanisms to Applications.ACS omega · 2026Review
- Hexagonal Close-Packed 2H-Cu Nanocrystals.Journal of the American Chemical Society · 2026Article
Corrections and comments
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Authors and funding
30 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
High-entropy alloy (HEA) nanomaterials are promising catalysts for proton exchange membrane water electrolysers (PEMWE), yet their crystalline structures have typically been restricted to thermodynamically stable phases. Here, using Au nanomaterials with distinct crystal phases as templates, we synthesize and stabilize Au@HEA core-shell nanostructures through a general and robust wet-chemical method in which the HEA is composed of up to ten metallic elements (Ir, Pt, Ni, Fe, Co, Rh, Pd, Ru, Cu and Mn). Phase-dependent water electrolysis is demonstrated as a proof-of-concept application. The hexagonal close-packed 4H-Au@4H-IrPtNiFeCo catalyst exhibits superior activity and stability for the acidic hydrogen evolution reaction, oxygen evolution reaction and overall water electrolysis compared with the conventional face-centred cubic IrPtNiFeCo catalyst. In a PEMWE at 60 °C, the 4H-Au@4H-IrPtNiFeCo catalyst achieves 3,000 mA cm
Identifiers
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Registered trials
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