Journal
RSC ADVANCES
Volume 12, Issue 14, Pages 8405-8413Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2ra00868h
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Funding
- Higher Education Commission (HEC) of Pakistan [20-14784/NRPU/RD/HEC/2021]
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This study presents a material design strategy to enhance the electrochemical activity of MXene sheets by introducing carbon nanotubes as conductive network channels. The hybrid catalyst exhibits improved activity for both hydrogen evolution reaction and oxygen evolution reaction, with good stability. This research opens up a new avenue for the development of cost-effective and efficient catalysts for clean hydrogen production.
Utilization of cost-effective, bifunctional, and efficient electrocatalysts for complete water splitting is desirable for sustainable clean hydrogen energy. In last decade, MXenes, a family of emerging two-dimensional (2D) materials with unique physiochemical properties, enticed scientists because of their use in different applications. However, insufficient electron transport, lower intrinsic chemical activity and limited active site densities are the factors inhibiting their use in electrocatalytic cells for hydrogen production. Here, we have presented material design to address this issue and introduced carbon nanotubes (CNTs) on V2CTx MXene sheets for conductive network channels that enhance the ion diffusion for enhanced electrochemical activity. The SEM reveals the uniform dispersion of the MWCNTs over the MXene surface that resulted in the formation of conductive network channels and enhances reaction kinetics. The as-synthesized electrocatalyst was subjected to linear sweep voltammetry (LSV) measurements for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The hybrid catalyst M2 exhibited an enhanced HER activity with a lower over-potential of 27 mV which is comparable to commercially available Pt-based catalysts (32 mV). Similarly, an enhanced OER activity was observed with a lower over-potential of 469 mV as compared to pristine V2CTx MXene. The electrocatalyst was subjected to a durability test through chronoamperometry and was observed to be stable for 16 hours. Hence, this study opens a new avenue for future cost-effective efficient catalysts for overall water splitting as a solution to produce clean hydrogen.
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