4.7 Article

Enabling methanol oxidation by an interacting hybrid nanosystem of spinel Co3O4 nanoparticle decorated MXenes

Journal

DALTON TRANSACTIONS
Volume 51, Issue 11, Pages 4324-4337

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt03671h

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Funding

  1. UGC

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In this study, a new type of nanocomposite Ti3C2/Co3O4 is proposed, which exhibits high electrocatalytic performance and durability in direct methanol fuel cells. The nanocomposite has a large surface area and a short charge carrier transport path, significantly improving the efficiency of the methanol oxidation reaction. In addition, the nanocomposite also shows a low onset potential, high oxidation current density, and good cycling stability.
For the successful implementation of direct methanol fuel cells in commercial applications, highly efficient and durable non-noble electrocatalysts based on conducting and stable non-carbonaceous supports can be potential candidates. Herein, spinel Co3O4 nanoparticles are decorated over Ti3C2 MXene nanosheets for methanol oxidation. The hybrid nanosystem Ti3C2/Co3O4 (TC) reduces restacking of MXene nanosheets, which offers a larger surface area for Co3O4 dispersion, leading to a shorter path for the charge carriers. TC coated on glassy carbon (GC) exhibits a MOR current density of 38.38 A g(-1) which is 2.9 times higher than that of Co3O4/GC in 1.5 M methanol at a 20 mV s(-1) scan rate. The hydrophilic terminations on the surface of MXenes create strong interactions with the Co3O4 nanoparticles, which increase the MOR kinetics of the nanocomposite. A low onset potential (0.32 V), high oxidation current density of the nanocomposite, efficient durability and cycling stability up to 200 CV cycles make this nanocomposite a better alternative to the state-of-the-art noble-metal electrocatalysts.

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