A Self‐Supported High‐Entropy Metallic Glass with a Nanosponge Architecture for Efficient Hydrogen Evolution under Alkaline and Acidic Conditions. (30th May 2021)
- Record Type:
- Journal Article
- Title:
- A Self‐Supported High‐Entropy Metallic Glass with a Nanosponge Architecture for Efficient Hydrogen Evolution under Alkaline and Acidic Conditions. (30th May 2021)
- Main Title:
- A Self‐Supported High‐Entropy Metallic Glass with a Nanosponge Architecture for Efficient Hydrogen Evolution under Alkaline and Acidic Conditions
- Authors:
- Jia, Zhe
Nomoto, Keita
Wang, Qing
Kong, Charlie
Sun, Ligang
Zhang, Lai‐Chang
Liang, Shun‐Xing
Lu, Jian
Kruzic, Jamie J. - Abstract:
- Abstract: Developing highly efficient and durable electrocatalysts for hydrogen evolution reaction (HER) under both alkaline and acidic media is crucial for the future development of a hydrogen economy. However, state‐of‐the‐art high‐performance electrocatalysts recently developed are based on carbon carriers mediated by binding noble elements and their complicated processing methods are a major impediment to commercialization. Here, inspired by the high‐entropy alloy concept with its inherent multinary nature and using a glassy alloy design with its chemical homogeneity and tunability, we present a scalable strategy to alloy five equiatomic elements, PdPtCuNiP, into a high‐entropy metallic glass (HEMG) for HER in both alkaline and acidic conditions. Surface dealloying of the HEMG creates a nanosponge‐like architecture with nanopores and embedded nanocrystals that provides abundant active sites to achieve outstanding HER activity. The obtained overpotentials at a current density of 10 mA cm −2 are 32 and 62 mV in 1.0 m KOH and 0.5 m H2 SO4 solutions, respectively, outperforming most currently available electrocatalysts. Density functional theory reveals that a lattice distortion and the chemical complexity of the nanocrystals lead to a strong synergistic effect on the electronic structure that further stabilizes hydrogen proton adsorption/desorption. This HEMG strategy establishes a new paradigm for designing compositionally complex alloys for electrochemical reactions.Abstract: Developing highly efficient and durable electrocatalysts for hydrogen evolution reaction (HER) under both alkaline and acidic media is crucial for the future development of a hydrogen economy. However, state‐of‐the‐art high‐performance electrocatalysts recently developed are based on carbon carriers mediated by binding noble elements and their complicated processing methods are a major impediment to commercialization. Here, inspired by the high‐entropy alloy concept with its inherent multinary nature and using a glassy alloy design with its chemical homogeneity and tunability, we present a scalable strategy to alloy five equiatomic elements, PdPtCuNiP, into a high‐entropy metallic glass (HEMG) for HER in both alkaline and acidic conditions. Surface dealloying of the HEMG creates a nanosponge‐like architecture with nanopores and embedded nanocrystals that provides abundant active sites to achieve outstanding HER activity. The obtained overpotentials at a current density of 10 mA cm −2 are 32 and 62 mV in 1.0 m KOH and 0.5 m H2 SO4 solutions, respectively, outperforming most currently available electrocatalysts. Density functional theory reveals that a lattice distortion and the chemical complexity of the nanocrystals lead to a strong synergistic effect on the electronic structure that further stabilizes hydrogen proton adsorption/desorption. This HEMG strategy establishes a new paradigm for designing compositionally complex alloys for electrochemical reactions. Abstract : A high‐entropy metallic glass with multinary nature and chemical homogeneity is developed by a scalable metallurgical technique. Dealloying creates a nanosponge‐like architecture with embedded nanocrystals that provides abundant active sites to achieve outstanding hydrogen evolution activity in both alkaline and acidic conditions. This work will provide a roadmap for designing alloy catalysts for many years to come. … (more)
- Is Part Of:
- Advanced functional materials. Volume 31:Number 38(2021)
- Journal:
- Advanced functional materials
- Issue:
- Volume 31:Number 38(2021)
- Issue Display:
- Volume 31, Issue 38 (2021)
- Year:
- 2021
- Volume:
- 31
- Issue:
- 38
- Issue Sort Value:
- 2021-0031-0038-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-05-30
- Subjects:
- chemical complexity -- electrocatalysis -- high‐entropy metallic glass -- lattice distortion -- metallurgy
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.202101586 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23813.xml