Multifunctional Ni 3 S 2 @NF-based electrocatalysts for efficient and durable electrocatalytic water splitting

Transition-metal sulfides (TMSs) have indeed drawn dramatic interest as a potential species of electrocatalysts by virtue of their unique structural features. However, their poor stability and inherent activity have impeded their use in electrocatalytic water splitting. Here, we provide a rational d...

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Veröffentlicht in:Dalton transactions : an international journal of inorganic chemistry 2023-09, Vol.52 (35), p.12378-12389
Hauptverfasser: Xu, Xiaomei, Mo, Qiaoling, Zheng, Kuangqi, Xu, Zhaodi, Cai, Hu
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Sprache:eng
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Zusammenfassung:Transition-metal sulfides (TMSs) have indeed drawn dramatic interest as a potential species of electrocatalysts by virtue of their unique structural features. However, their poor stability and inherent activity have impeded their use in electrocatalytic water splitting. Here, we provide a rational design of a hierarchical nanostructured electrocatalyst containing CeO x -decorated NiCo-layered double hydroxide (LDH) coupled with Ni 3 S 2 protrusions formed on a Ni foam (NF). Specifically, the as-prepared electrocatalyst, denoted as Ni 2 Co 1 LDH-CeO x /Ni 3 S 2 @NF, presents only 250 and 300 mV overpotential at ±100 mA cm −2 , respectively, along with the Tafel slope values of 92 and 52 mV dec −1 , as well remarkable long-term life for water splitting in an alkaline electrolyte. Based on systematic experiments and theoretical analysis, the superior electrocatalytic property in terms of Ni 2 Co 1 LDH-CeO x /Ni 3 S 2 @NF can be imputed to the following reasons: the porous framework of Ni 3 S 2 @NF provides a largely surface area and high conductivity; the NiCo LDH nanosheets provide enriched active sites and favorable adsorption ability; the oxygen-vacancy-rich CeO x optimizes the electronic configuration. Overall, these factors work synergistically to expedite the catalytic kinetics of splitting water. Our work concentrates on a rational interface to devise efficient, multifunctional, and serviceable electrocatalysts for future applications.
ISSN:1477-9226
1477-9234
DOI:10.1039/D3DT02035E