Nonprecious and shape-controlled Co3O4-CoO@Co electrocatalysts with defect-rich and spin-state altering properties to accelerate hydrogen evolution reaction at large current densities over a wide pH range

[Display omitted] •Morphology-dependent Heterointerface Co3O4-CoO@Co catalysts are successfully synthesized.•The SPH-Co3O4-CoO@Co catalyst requires ultra-low overpotential to drive the 50 mAcm−2 over a wide pH range.•Benefitting from the defective sites and electronic structure engineering, the SPH-...

Full description

Saved in:
Bibliographic Details
Published inChemical engineering journal (Lausanne, Switzerland : 1996) Vol. 495; p. 153442
Main Authors Karuppasamy, Lakshmanan, Gurusamy, Lakshmanan, Anandan, Sambandam, Barton, Scott C., Liu, Cheng-Hua, Wu, Jerry J.
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.09.2024
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:[Display omitted] •Morphology-dependent Heterointerface Co3O4-CoO@Co catalysts are successfully synthesized.•The SPH-Co3O4-CoO@Co catalyst requires ultra-low overpotential to drive the 50 mAcm−2 over a wide pH range.•Benefitting from the defective sites and electronic structure engineering, the SPH-Co3O4-CoO@Co exhibits a large current density. In this study, efficient HER activity is achieved through the successful preparation of Co3O4-CoO@Co catalysts that are morphology-dependent. It is proposed that the distinctive skeletal polyhedron (SPH) morphology of the Co3O4-CoO@Co catalyst shows outstanding HER performances over the universal pH range. The heterostructure catalyst exhibits a current density of 50 mAcm−2 at an ultra-low overpotential of 28, 62, and 138 mV under 0.5 M H2SO4, 1 M KOH, and 1 M PBS electrolytes, respectively. Experimental and theoretical studies indicate that electron-enriched Co2+ in the CoO site is favorable for H+ cation adsorption and high valence Co3+ in the Co3O4 site is favorable for H2O molecule activation and dissociation in acidic, neutral, and alkaline electrolytes. Benefitting from an empty eg 3d orbital with a strong Jahn–Teller effect, a high density of spin states, and a large number of oxygen vacancies, the SPH-Co3O4-CoO@Co catalyst is demonstrated to provide faster hydrogen evolution reaction.
ISSN:1385-8947
DOI:10.1016/j.cej.2024.153442