Hierarchical Superhydrophilic/Superaerophobic Ni3S2/VS2 Nanorod-Based Bifunctional Electrocatalyst Supported on Nickel Foam for Overall Urea Electrolysis

Yuxing Huang*, Hui Xu, Yamei Wang, Ziyan Xing, Ruochao Fang, Huihuang Lai, Man Qian, Mingdong Dong, Mauro Carraro, Troels Skrydstrup*, Kim Daasbjerg*, Zhuo Xin*

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

Abstract

The design and preparation of effective nonprecious metal-based catalysts for the urea oxidation reaction (UOR) coupled with the hydrogen evolution reaction (HER) are of great significance to solve both energy shortage and environmental pollution problems. In this study, a novel hierarchical superhydrophilic and superaerophobicity three-dimensional nanorod-like bifunctional catalyst with a heterostructure (Ni3S2/VS2) was prepared on nickel foam via a simple one-step hydrothermal method, serving as an excellent electrocatalyst for both UOR and HER. The formed heterostructure significantly alters the electronic structure, optimizing charge transfer and increasing the number of active sites, which enhances the electrocatalytic performance of Ni3S2/VS2. As a result, this catalyst requires an extremely low potential of 1.396 V at the current density of 100 mA cm-2 for UOR and only 164 mV overpotential at -10 mA cm-2 for HER. Notably, a constructed two-electrode electrolyzer system (Ni3S2/VS2∥Ni3S2/VS2) demonstrates extraordinary activity and long-term stability, achieving a current density of 10 mA cm-2 at a low cell voltage of 1.48 V, which is superior to majority of the reported catalysts. This work demonstrates that the formation of heterostructures can effectively enhance the catalytic activity of nanomaterials toward UOR and HER and provides a feasible strategy for fabricating highly efficient nonprecious metal overall urea electrocatalysts.

OriginalsprogEngelsk
TidsskriftInorganic Chemistry
Vol/bind63
Nummer40
Sider (fra-til)19002-19010
Antal sider9
ISSN0020-1669
DOI
StatusUdgivet - 7 okt. 2024

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