Karlo Maškarić, Ana Varadi, Ameen Uddin Ammar, Adriana Popa, Dana Toloman, Sergiu Macavei, Lucian Barbu–Tudoran, Cristian Leoștean, Emre Erdem, Maria Ștefan, Arpad Mihai Rostas
This research underscores the promising potential of SnO 2 -based materials in high-performance supercapacitor applications, with and ions serving as dopants. A range of characterization and testing was performed to examine SnO 2 as an electrode material, focusing on understanding the influence of W ions on its electrochemical properties. Techniques such as scanning and transmission electron microscopy, X-ray diffraction, Raman spectroscopy, and photoluminescence spectroscopy were employed to analyze the morphology and structure. Changes in defect structures due to W-doping and its oxidation state were detected via electron paramagnetic resonance and X-ray photoelectron spectroscopy, confirming the presence of / redox pairs. An exhaustive electrochemical examination of undoped and W-doped SnO 2 was performed, tested as electrodes in all-in-one symmetrical supercapacitor setups, with detailed performance assessments following. Results indicated that W addition significantly enhanced the specific capacitance of the host material, achieving a specific capacitance of 268 F/g at a 0.5% W ion concentration, along with improved energy and power densities of 36.8 Wh/kg and 2650 W/kg, respectively. This enhancement is attributed to the variable valence states of W ions, with the mixed / state enhancing faradaic reactions and facilitating rapid charge transfer through hopping processes between different cation valence states at relatively low activation energies. Dunn’s analysis of the best-performing supercapacitor device indicated that, at higher scan rates, capacitive processes dominate the energy storage mechanism, with electric double-layer capacitance and rapid surface redox reactions playing a key role, while at lower scan rates, diffusion-based processes become more significant. This suggests that, at lower scan rates, electrolyte ions can penetrate deeper pores and interact with the / redox-active sites introduced into the SnO 2 host.