# Isopropanol Electro-Oxidation on PtCu Alloys for Aqueous Organic Redox Chemistry Toward Energy Storage

**Authors:** Jinyao Tang, Xiaochen Shen, Laura Newsom, Rongxuan Xie, Parsa Pishva, Yanlin Zhu, Bin Liu, Zhenmeng Peng

PMC · DOI: 10.3390/molecules30194027 · 2025-10-09

## TL;DR

This paper explores using isopropanol and PtCu alloys in redox flow batteries for efficient and low-cost energy storage.

## Contribution

The study introduces PtCu alloys as effective electrocatalysts for isopropanol electro-oxidation in aqueous-organic redox flow batteries.

## Key findings

- PtCu catalysts achieved a low activation energy of 14.4 kJ/mol for isopropanol electro-oxidation.
- PtCu showed enhanced resistance to catalyst poisoning compared to pure Pt.
- A PtCu-catalyzed H-cell demonstrated stable cycling over 200 cycles.

## Abstract

Integration of renewable energy into modern power grids remains limited by intermittency and the need for reliable energy storage. Redox flow batteries (RFBs) are promising for large-scale energy storage, yet their widespread adoption is hindered by the high cost. In this study, we investigate isopropanol as a redox-active species with Pt-Cu alloy electrocatalysts for aqueous-organic RFBs. A series of PtxCu catalysts with varying Pt:Cu ratios were synthesized and studied for isopropanol electro-oxidation reaction (IPAOR) performance. Among them, PtCu demonstrated the best performance, achieving a low activation energy of 14.4 kJ/mol at 0.45 V vs. RHE and excellent stability at 1 M isopropanol (IPA) concentration. Kinetic analysis and in situ attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy revealed significantly reduced acetone accumulation on PtCu compared to pure Pt, indicating enhanced resistance to catalyst poisoning. Density functional theory (DFT) calculations further identified the first proton-coupled electron transfer (PCET) as the rate-determining step (RDS) with C-H bond scission as the preferred pathway on PtCu. A proof-of-concept PtCu-catalyzed H-cell demonstrated stable cycling over 200 cycles, validating the feasibility of IPA as a low-cost, regenerable redox couple. These findings highlight PtCu-catalyzed IPA/acetone(ACE) chemistry as a promising platform for next-generation aqueous-organic RFBs.

## Linked entities

- **Chemicals:** isopropanol (PubChem CID 3776), acetone (PubChem CID 180), Pt (PubChem CID 23939), Cu (PubChem CID 23978)

## Full-text entities

- **Chemicals:** IPA (MESH:D019840), Cu (MESH:D003300), acetone (MESH:D000096), Pt (MESH:D010984), PtCu (-), ACE (MESH:C024789), C (MESH:D002244)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12525896/full.md

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Source: https://tomesphere.com/paper/PMC12525896