Being a champion in a portable electronics world, lithium-ion batteries (LIBs) are irreplaceable, but the scarcity of Li, high cost, and the inclusion of non-aqueous electrolytes make them relatively perilous and inefficient for grid-scale energy storage. Recently, the blooming aqueous Zn-ion batteries (ZIBs) have emerged as one of the pioneer candidates featuring the inherently safe nature of metallic Zn anode and its unique properties.[1] Vanadium-based compounds show fast ion diffusion and excellent reversible capacity because of their rich valence state of vanadium, facile distortion of V-O polyhedrons, and tuneable composition, which offers an excellent treasure house. Moreover, the different oxidation states of vanadium allow a higher degree of structural change and greater functional flexibility while incorporating multivalent cations into vanadium-based compounds. [2] The present work focuses on one V-based oxide cathode. The cathode, ZnV2O4, synthesized by a simple solid-state route, showed a reversible capacity of around 200 mAh/g at a current density of 500 mA/g. Ex-situ XAS suggested that there is a drastic change in V and Zn local environment, confirming that there is a structural transformation taking place. Further, we have pursued ex-situ TEM where segregation of the conversion product phases was seen, confirmed by the small crystalline domains present at the nanoscale regime. A detailed analysis will be discussed to verify that a phase transformation is happening and is getting amorphized in subsequent cycles using ex-situ TEM and XAS.Also, metal-air batteries are widely discussed and studied because of their high energy density. In this pursuit, highly efficient bifunctional electrocatalysts, non-noble such as Co metal-based phosphates/oxides, have been studied vividly.[3,4] Herein, we present a thorough study of three-dimensional ZnCo2(PO4)2 (ZCP), which showed excellent bifunctional activity compared to the benchmark catalysts, denoting the presence of many catalytically active Co sites in ZCP. The presence of asymmetric edge-sharing CoO5/CoO6 polyhedra enhances the net catalytic activity.[5] ZCP exhibited robust oxygen reduction and evolution (ORR and OER) activity with the onset of 0.87 and 1.50 V vs. RHE for ORR and OER, respectively. The ORR saturated current density for ZCP was 6.38 mA/cm2, close to the 20% Pt/C catalyst benchmark. It also showed an OER exchange current density of 16.7 mA/cm2, closer to RuO2 ( j= 17.6 mA/cm2). This bifunctional electrocatalytic activity will be elaborated using analytical tools and DFT, along with the demonstration of Zn-air batteries. A detailed structural characterization using synchrotron refinement, TEM analysis, magnetic studies, and electrocatalysis performance will be discussed. Reference s : [1] M. Song et al., Adv. Funct. Mater. 2018, 28, 1802564.[2] Yao. Zhang et al., Chem. Front. 2021, 5 744-762.[3] J. L. Jung et al., Energy Environ. Sci. 2016, 9176-183.[4] W. Liu et al., Acc. Chem. Res . 2018,51,1858.[5] A. Baby et al., Chem. Comm. 2020, 56, 8400-8403.
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