Abstract

The electrochemical performance of 2-dimensional hybrid perovskite electrodes for Li-ion batteries are investigated using a high-molarity electrolyte. The effect of changing the halide content and layering structure is systematically explored.

Highlights

  • *d and Hybrid metal halide perovskites, typically known for their photovoltaic applications, have recently gained traction as a potential energy-storage material due to their promising gravimetric capacities as lithium-ion battery electrode materials

  • The hybrid perovskite materials are characterised using a combination of UV-vis absorption and X-ray diffraction (XRD) spectroscopy to confirm the characteristic shifts in the bandgap and crystallographic spacing associated with the layering order of the Ruddlesden Popper (RP) perovskite series

  • We demonstrate that out of the iodide and bromide based RP layered perovskite structures, an optimum composition for Li-ion batteries (LIBs) performance is reached with the n = 4 bromide species (BA)2(MA)3Pb4Br13

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Summary

Introduction

*d and Hybrid metal halide perovskites, typically known for their photovoltaic applications, have recently gained traction as a potential energy-storage material due to their promising gravimetric capacities as lithium-ion battery electrode materials. Higher gravimetric discharge capacities have subsequently been reported by Tathavadekar et al.[15] for the one-dimensional (1D) benzidine lead iodide with needlelike morphology of 646 mA h gÀ1, 508 mA h gÀ1 for the twodimensional (2D) layered butylammonium (BA) lead iodide (BAPbI4), and 202 mA h gÀ1 for the traditional MAPbI3 bulk phase after 50 cycles. While these capacities are promising, compared to commercial graphite anodes (theoretical capacity of 372 mA h gÀ1 ),[16] relatively little attention and resource have been dedicated to the further development of this application due to the unstable behaviour of hybrid perovskites. Paper in the Li-ion battery environment.[17,18,19] the composition-function and structure–function relationships for hybrid perovskite electrodes remain poorly understood

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