Specific Cu Active Sites of CuO Cluster Loading SnO2 for Sensitive EMC Detection in Lithium-Ion Batteries

Conventional metal oxide sensors often lack sufficient sensitivity due to limited adsorption sites. Loading clusters is an effective surface-modification strategy. In this work, CuO clusters of approximately 3 nm were highly dispersed on high-surface-area SnO2 nanoboxes. TEM confirmed the cluster sizes and dispersion degrees of the CuO clusters, while Raman and XPS collectively confirmed that CuO modifies the electronic structure of the SnO2 support and induces the formation of new oxygen vacancies. The optimized Cu/SN-2 sensor exhibited a response of 39.25 toward 10 ppm ethyl methyl carbonate (EMC) at 130 °C, which is 1.92 times higher than that of SnO2 nanoboxes (20.46 at 140 °C). The diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) indicated that CuO lowers the activation energy for EMC decomposition, producing intermediates like CO2, methanol, and ethanol at lower temperatures, thus reducing the sensor operating temperature. The density functional theory (DFT) calculations confirmed that Cu sites act as negatively charged centers, promoting EMC adsorption and enhancing sensitivity. This work offers a simple, low-cost surface modification route to improve gas sensing. Furthermore, as EMC is a common electrolyte in lithium-ion batteries, its leakage poses safety risks. Integrating such EMC sensors into battery safety systems can enable ultraearly leak warnings, helping prevent fires and explosions.