Enhancement of Photocurrent by Reducing Charge Recombination at the Core–Shell Interface of Sm3+-Doped ZnO Nanoparticles and Studies on Photostability
摘要
In this study, we report the green synthesis of core–shell heterostructured Sm3+-doped ZnO (10 wt.%) and evaluate its role in structural, morphological, photocurrent, and photocorrosion stability enhancement in comparison to undoped ZnO. Both synthesized materials demonstrated outstanding stability as confirmed by X-ray diffraction (XRD), where the ZnO phase remained stable before and after photocurrent measurement, indicating high structural integrity. Transmission electron microscopy (TEM) revealed the formation of a core–shell heterostructure, which was further supported by Brunauer–Emmett–Teller (BET) analysis, showing an improved surface area of Sm3+-doped ZnO due to the modified morphology. After Sm3+ doping, photoluminescence (PL) quenching is observed due to non-radiative recombination and cross-relaxation processes. Raman spectroscopy confirmed the characteristic peaks of ZnO, with a decrease in intensity upon Sm3+ doping. Photocurrent measurement using linear sweep voltammetry (LSV) demonstrated enhanced current response from 1.01 to 2.31 mA/cm2 after doping, while chronoamperometry confirmed the long-term stability of the doped material. The combination of structural stability, improved surface area, and enhanced photocurrent suggests that Sm3+-doped ZnO with a core–shell heterostructure has great potential as an electron transport layer (ETL)/photo-absorber material for future photovoltaic devices offering enhanced stability and efficiency.
Graphical Abstract