Construction of Heterostructure between Ni17W3 and WO2 to Boost the Hydrogen Oxidation Reaction in Alkaline Medium

The inferior intrinsic performance of Ni-based catalysts for the hydrogen oxidation reaction (HOR) in an alkaline medium seriously restricts the utilization of emerging anion-exchange membrane fuel cells (AEMFCs). This is because the hydrogen and hydroxyl binding energies on Ni need to be optimized. Although electrocatalysts obtained by alloying Ni with Mo or W reportedly exhibit enhanced activity, they are still far from industrial requirements based on unbalanced HBE and OHBE. Herein, we report to further enhance alkaline HOR activity by constructing a heterostructure between NiW alloy and metal oxide (Ni17W3/WO2), which is synthesized through solvothermal treatment combined with annealing. The as-fabricated reduced graphene oxide (rGO)-supported Ni17W3/WO2 (Ni17W3/WO2/rGO) exhibits state-of-the-art catalytic activity (current density of 2.9 mA cm-2 at 0.1 V vs RHE), faster kinetics (geometric kinetics current density of 4.0 mA cm-2 that can be comparable to Pt/C), and high stability (maintaining the current density for more than 80 h) toward HOR in alkaline media. The detailed characterizations reveal that the charge transfer across the boundary arising from constructing the as-prepared heterostructure tunes the electronic structures, ultimately facilitating the HOR process.

Medienart:

E-Artikel

Erscheinungsjahr:

2024

Erschienen:

2024

Enthalten in:

Zur Gesamtaufnahme - year:2024

Enthalten in:

ACS applied materials & interfaces - (2024) vom: 12. Jan.

Sprache:

Englisch

Beteiligte Personen:

Zhang, Bin [VerfasserIn]
Qiu, Xinzhuo [VerfasserIn]
Chen, Tingzhao [VerfasserIn]
Huang, Churong [VerfasserIn]
Yue, Xin [VerfasserIn]
Huang, Shaoming [VerfasserIn]

Links:

Volltext

Themen:

Alkaline medium
Anion exchange membrane fuel cells
Heterostructure
Hydrogen oxidation reaction
Journal Article
Nonprecious metal electrocatalyst

Anmerkungen:

Date Revised 12.01.2024

published: Print-Electronic

Citation Status Publisher

doi:

10.1021/acsami.3c13952

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM367045931