# Platinum Group Metal (PGM) free multi metallic nanomaterial: a potential electrocatalyst for Ethanol Oxidation

**Authors:** Susmita SINGH, Prodipta PAL, Soumik ROY, Shalini BASAK, Prantica SAHA, Anushna DUTTA, Sinthia SAHA, Mainak BOSE

PMC · DOI: 10.55730/1300-0527.3709 · Turkish Journal of Chemistry · 2024-10-14

## TL;DR

This paper explores a cost-effective, non-toxic electrocatalyst for ethanol oxidation in fuel cells, using a PGM-free nanomaterial.

## Contribution

A PGM-free multi-metallic nanomaterial is developed and shown to efficiently promote ethanol oxidation through a bifunctional mechanism.

## Key findings

- The C/Fe50Co50 catalyst demonstrates high catalytic efficiency for ethanol oxidation.
- The catalyst promotes CO removal via a bifunctional mechanism and electronic effect.
- Physical and electrochemical analyses reveal the catalyst's active site and oxidation kinetics.

## Abstract

Comprehensive studies of the ethanol oxidation reaction (EOR) have shown high interest in fuel cell technologies. As anode catalysts, introducing platinum group metal (PGM) free catalyst is promising for higher catalytic activity towards the EOR, as these are cost-effective, pollution-tolerant, and suitable for sustainable energy conversion. In this investigation, multi walled carbon nanotube (MWCNT) supported PGM-free electrocatalysts are synthesized by the impregnation reduction method. The atomic structure, composition, and morphology of nanoalloy catalysts are discovered through X-ray diffraction (XRD), Raman spectroscopy and fourier-transform infrared (FTIR) spectroscopy techniques. Electrochemical behaviours have been analysed by cyclic voltammetry (CV), linear sweep voltammetry (LSV), Chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS), which reveal the oxidation kinetics of ethanol in an alkaline medium on the surface of the catalyst. The structure-activity relationship is a portrait of all the physical and electrochemical analyses that assists in exploring the active site of the surface, which facilitates electrooxidation activity. The C/Fe50Co50 catalyst exhibits higher catalytic efficiency and promotes CO removal through a bifunctional mechanism and electronic effect.

## Linked entities

- **Chemicals:** ethanol (PubChem CID 702), CO (PubChem CID 281)

## Full-text entities

- **Chemicals:** Ethanol (MESH:D000431), C (MESH:D002244), Fe50Co50 (-), CO (MESH:D002248)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11913351/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC11913351/full.md

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Source: https://tomesphere.com/paper/PMC11913351