Diffusionless-Like Transformation Unlocks Pseudocapacitance with Bulk Utilization: Reinventing Fe2O3 in Alkaline Electrolyte

Energy density can be substantially raised and even maximized if the bulk of an electrode material is fully utilized. Transition metal oxides based on conversion reaction mechanism are the imperative choice due to either constructing nanostructure or intercalation pseudocapacitance with their intrinsic limitations. However, the fully bulk utilization of transition metal oxides is hindered by the poor understanding of atomic-level conversion reaction mechanism, particularly it is largely missing at clarifying how the phase transformation (conversion reaction) determines the electrochemical performance such as power density and cyclic stability. Herein, alpha-Fe2O3 is a case provided to claim how the diffusional and diffusionless transformation determine the electrochemical behaviors, as of its conversion reaction mechanism with fully bulk utilization in alkaline electrolyte. Specifically, the discharge product alpha-FeOOH diffusional from Fe(OH)(2) is structurally identified as the atomic-level arch criminal for its cyclic stability deterioration, whereas the counterpart delta-FeOOH is theoretically diffusionless-like, unlocking the full potential of the pseudocapacitance with fully bulk utilization. Thus, such pseudocapacitance, in proof-of-concept and termed as conversion pseudocapacitance, is achieved via diffusionless-like transformation. This work not only provides an atomic-level perspective to reassess the potential electrochemical performance of the transition metal oxides electrode materials based on conversion reaction mechanism but also debuts a new paradigm for pseudocapacitance.

Automated summary

This study investigates the conversion reaction mechanism of α-Fe2O3 and reveals the impact of diffusional and diffusionless transformation on electrochemical performance, as well as a method to achieve pseudocapacitance through diffusionless transformation.