Three-dimensional bimodal pore-rich G/MXene sponge amalgamated with vanadium diselenide nanosheets as a high-performance electrode for electrochemical water-oxidation/reduction reactions

Exploring new strategies to design non-precious and efficient electrocatalysts can provide a solution for sluggish electrocatalytic kinetics and sustainable hydrogen energy. Transition metal selenides are potential contenders for bifunctional electrocatalysis owing to their unique layered structure,...

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Published inDalton transactions : an international journal of inorganic chemistry Vol. 53; no. 19; pp. 8177 - 819
Main Authors Chaudhary, Khadija, Zulfiqar, Sonia, ALOthman, Zeid A, Shakir, Imran, Warsi, Muhammad Farooq, Cochran, Eric W
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 14.05.2024
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Summary:Exploring new strategies to design non-precious and efficient electrocatalysts can provide a solution for sluggish electrocatalytic kinetics and sustainable hydrogen energy. Transition metal selenides are potential contenders for bifunctional electrocatalysis owing to their unique layered structure, low band gap, and high intrinsic activities. However, insufficient access to active sites, lethargic water dissociation, and structural degradation of active materials during electrochemical reactions limit their activities, especially in alkaline media. In this article, we report a useful strategy to assemble vanadium diselenide (VSe 2 ) into a 3D MXene/rGO-based sponge-like architecture (VSe 2 @G/MXe) using hydrothermal and freeze-drying approaches. The 3D hierarchical meso/macro-pore rich sponge-like morphology not only prevents aggregation of VSe 2 nanosheets but also offers a kinetics-favorable framework and high robustness to the electrocatalyst. Synergistic coupling of VSe 2 and a MXene/rGO matrix yields a heterostructure with a large specific surface area, high conductivity, and multi-dimensional anisotropic pore channels for uninterrupted mass transport and gas diffusion. Consequently, VSe 2 @G/MXe presented superior electrochemical activity for both the HER and OER compared to its counterparts (VSe 2 and VSe 2 @G), in alkaline media. The overpotentials required to reach a cathodic and anodic current density of 10 mA cm −2 were 153 mV (Tafel slope = 84 mV dec −1 ) and 241 mV (Tafel slope = 87 mV dec −1 ), respectively. The R ct values at the open circuit voltage were as low as 9.1 Ω and 1.41 Ω for the HER and OER activity, respectively. Importantly, VSe 2 @G/MXe withstands a steady current output for a long 24 h operating time. Hence, this work presents a rational design for 3D microstructures with optimum characteristics for efficient bifunctional alkaline water-splitting. A three-dimensional hierarchical G/MXe sponge integrated with VSe 2 sheets as advanced electrode material for water-splitting.
Bibliography:C
results for VSe
G/MXe for the OER (Fig. S8), comparison of the HER performance of VSe
G/MXe (Fig. S1), XRD patterns of MXene and rGO (Fig. S2)
G/MXe with that of similar reported electrocatalytic materials (Table S2). See DOI
G/MXe with that of similar reported electrocatalytic materials (Table S1), and comparison of the OER performance of VSe
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VSe
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G, and VSe
G/MXe (Fig. S6), ECAS-normalized LSV curves of VSe
Electronic supplementary information (ESI) available: EDX spectra of (a) VSe
https://doi.org/10.1039/d4dt00602j
2
(b) VSe
V
G, and (c) VSe
profiles of VSe
and VSe
G/MXe (Fig. S3), LSV curve of G/MXe for the HER (Fig. S4), LSV curve of G/MXe for the OER (Fig. S5)
G/MXe for the HER (Fig. S7), ECAS-normalized LSV curves of VSe
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ISSN:1477-9226
1477-9234
DOI:10.1039/d4dt00602j