Abstract
This paper proposes NiCoW@Ti3C2 MXene composite as a non-noble metal-based catalyst, utilizing a strong metal-support interaction strategy through a facile one-step hydrothermal approach. Through physicochemical characterizations, the well-formed heterostructure is confirmed at NiCoW/Ti3C2 MXene interface. Notably, electrochemical evaluations reveal that NiCoW@Ti3C2 (20 wt%) electrocatalyst exhibits superior activity for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), exhibiting lower onset potentials for HER (0.107 and 0.222 V) and OER (0.244 and 0.328 V) at current densities of 100 and 300 mA/cm2, surpassing values are reported by recent catalysts. The water-splitting device, utilizing the NiCoW@Ti3C2 (20 wt%) as a bifunctional electrode, achieves a lower voltage of 1.51 V to achieve a current density of 10 mA/cm2. Density functional theory (DFT) calculations further elucidate the enhanced HER/OER activity of the hybrid NiCoW/Ti3C2 surface. Additionally, stability is assessed using time series analysis (TSA), which accurately predicts the experimental potential (E) trends, confirming TSA's applicability for modeling the cell's electrochemical behavior. Methanol oxidation reaction (MOR) activity is also extensively explored in alkaline media, demonstrating strong electrocatalytic performance due to the synergistic effects of Ni, Co, W, and 2D MXene. These findings position NiCoW/Ti3C2 as a promising multifunctional catalyst for sustainable energy conversion applications.
| Original language | British English |
|---|---|
| Article number | 237675 |
| Journal | Journal of Power Sources |
| Volume | 652 |
| DOIs | |
| State | Published - 1 Oct 2025 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Density functional theory (DFT)
- Hydrogen evolution reaction
- Methanol oxidation reaction
- MXene modified NiCoW
- Oxygen evolution reaction
- Time series analysis
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