Synergistic Heterostructure Catalyst for Enhanced CO2-to-C2 Conversion and High-Performance Aqueous Zn-CO2 Batteries
Muhammad Kashif Aslam1, Iftikhar Hussain2, Sidra Hameed3
1Department of Chemical and Petroleum Engineering College of Engineering UAE University Al Ain 15551 Abu Dhabi United Arab Emirates.
Abstract:
This study investigates the synergistic interaction of CuO and SnO2 in a heterostructure catalyst (CuO@SnO2) for the conversion of C1 carbon dioxide (CO2) reduction products to C2 products and its application in high-performance aqueous Zn-CO2 batteries. This synergistic combination enhances the Faradaic efficiency (FE) for ethanol production from 12.5% to 41.8%, shifting the selectivity from C1 to C2 products. The flow-type aqueous Zn-CO2 battery exhibits an ultrahigh power density of 6.5 mW cm-2, demonstrates a high discharge voltage of 0.9 V, and maintains stable operation over 140 cycles, underscoring the catalyst's exceptional reversibility and durability. During battery discharge, the system achieves a FE of 36.86% for ethanol production. These results highlight the pivotal role of the CuO@SnO2 synergy in optimizing CO2 conversion efficiency while generating electrical energy. The findings advance the development of dual-function energy storage systems that integrate renewable electricity generation with sustainable CO2 utilization, paving the way for industrial-scale applications.
More Related Videos
10:15Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
10:57Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
Published on: April 10, 2018
Related Concept Videos
Batteries and Fuel Cells
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Catalysis
