Engineering rGO@CeO2/Co3O4 nanocomposite for dual-functional electrocatalysis in solar energy conversion and environmental remediation
摘要
The multifunctional rGO@CeO2/Co3O4 nanocomposite, designed for solar energy conversion, and pollutant degradation applications, was successfully synthesized using a sol–gel approach. Structural, morphological, and chemical analyses were performed using XRD, SEM, and XPS techniques. XRD results confirmed the crystalline phases of CeO2 and Co3O4, while the absence of the characteristic rGO peak indicated its uniform dispersion within the composite matrix. SEM observations revealed that the incorporation of rGO transformed the aggregated morphology into interconnected nanosheet structures, providing a conductive network that reduced particle agglomeration and enhanced charge transport. XPS analysis confirmed the coexistence of Ce4+/Ce3+ and Co3+/Co2+ oxidation states, indicating strong interfacial electronic interactions between rGO and the metal oxides. Owing to the synergistic effect of improved conductivity, efficient charge separation, and increased active surface area, the rGO@CeO2/Co3O4 electrode exhibited superior electrochemical performance. When employed as a counter electrode in dye-sensitized solar cells (DSSCs), the hybrid nanocomposite achieved a power conversion efficiency of 9.2 ± 0.02%, exceeding both CeO2/Co3O4 and conventional Pt electrodes. In photocatalytic studies, the composite demonstrated an excellent tetracycline degradation efficiency of 98%, significantly higher than the comparison electrodes. The enhanced multifunctional performance is mainly attributed to the synergistic interaction between rGO and CeO2/Co3O4, which facilitates rapid electron transport, suppresses charge recombination, and increases the number of active catalytic sites. These findings demonstrate the potential of rGO@CeO2/Co3O4 as an efficient and sustainable material for next-generation photoelectrochemical and environmental remediation applications.