RESUMO
MXenes have attracted considerable attention in the field of energy storage and conversion due to their high surface area, excellent electrical conductivity, and ability to intercalate various ions. However, simultaneously achieving high capacitance, rate capability, cycling stability, and mechanical flexibility is a significant challenge for designing MXene-based supercapacitors. In this article, we explored MXene-BiFeO3-ZnO nanocomposites for both photocatalytic and electric double-layer supercapacitor applications. While the BiFeO3-ZnO nanohybrid heterostructure improves the charge separation properties in nanocomposite photocatalysts, it was applied as an interlayer spacer between the MXene layers to prevent the stacking effect of electrodes in the supercapacitor. Furthermore, the optimization of MXene content in the nanocomposite was established by photocatalytic studies on methylene blue dye, which revealed a maximum of 98.72% degradation under direct sunlight with superior stability. The electrochemical studies on the best composition material reveal a maximum areal capacitance (Ccv) of 142.8 mF cm-2, an energy density (E) of 1.65 µW h cm-2, and a capacitive retention of 99.98% after 8000 cycles at 7 µA cm-2. Additionally, the flexible solid-state supercapacitor fabricated with the same material demonstrates an areal capacitance of 47.6 mF cm-2 and a capacitive retention of 66% after 8000 cycles at 7 µA cm-2, with potential for high-performance flexible supercapacitors.
RESUMO
Spin-orbit coupling offers a large variety of novel and extraordinary magnetic and electronic properties in otherwise 'ordinary pool' of heavy ion oxides. Here we present a detailed study on an apparently isolated hexagonal 2Hspin-chaind4iridate Sr3LiIrO6with geometric frustration. Our structural studies reveal Li-Ir chemical order with desired stoichiometry in this compound, while x-ray absorption together with x-ray photoemission spectroscopic characterizations establish pure 5+ valence of Ir. We have established a magnetic ground state with finite Ir5+magnetic moments in this compound, contrary to the anticipated nonmagneticJeff= 0 state, through combined dc susceptibility,7Li nuclear magnetic resonance (NMR), muon spin relaxation (µSR) andab-initioelectronic structure studies. These investigations together with ac magnetic susceptibility and specific heat measurements reveal that despite having noticeable antiferromagnetic correlation among the Ir5+local moments, this system does not magnetically order down to at least 0.05 K, possibly due to geometrical exchange frustration, arising from the comparable nearest- and next-nearest-neighbor interchain Ir-O-O-Ir superexchange interaction strengths with opposite signs. However, the zero-fieldµSR analysis shows emergence of a considerable proportion of spin-freezing on top of a spin-fluctuating dynamic magnetic background down to the lowest measured temperature of 1.7 K, possibly due to some inhomogeneity and/or the much stronger intra-column Ir-Ir magnetic exchange interaction strength relative to the inter-column Ir-Ir ones. The linear temperature dependence of the magnetic specific heat (Cm) in both zero and applied magnetic fields, plus the power-law behavior of the NMR spin-lattice relaxation rate suggest a gapless spinon density of states in this charge gapped disordered magnetic ground state of Sr3LiIrO6.