Effect of Mn Substitution on GeFe2O4 as an Anode for Sodium Ion Batteries

Author:

Ambrosetti Marco12,Rocchetta Walter1,Quinzeni Irene2,Milanese Chiara13ORCID,Berbenni Vittorio1,Bini Marcella134ORCID

Affiliation:

1. Chemistry Department, University of Pavia, Viale Taramelli 16, 27100 Pavia, Italy

2. RSE—Ricerca Sul Sistema Energetico, Via R. Rubattino 54, 20134 Milano, Italy

3. C.S.G.I., Consorzio Per i Sistemi a Grande Interfase, Via Della Lastruccia 3, 50019 Sesto Fiorentino (FI), Italy

4. National Reference Centre for Electrochemical Energy Storage (GISEL)-INSTM, Via G. Giusti 9, 50121 Firenze, Italy

Abstract

GeFe2O4 (GFO), with its intriguing intercalation mechanism based on alloying–conversion reactions, was recently proposed as an anode material for sodium ion batteries (SIBs). However, drawbacks related to excessive volume expansion during intercalation/deintercalation and poor electronic conductivity enormously hinder its practical application in batteries. In this regard, some experimental strategies such as cation substitutions and proper architectures/carbon coatings can be adopted. In this paper, pure and Mn-doped GFO samples were prepared by hydrothermal synthesis. The doped samples maintained the spinel cubic structure and the morphology of pure GFO. The electrochemical tests of the samples, performed after proper carbon coating, showed the expected redox processes involving both Ge and Fe ions. The Mn doping had a positive effect on the capacity values at a low current density (about 350 mAh/g at C/5 for the Mn 5% doping in comparison to 300 mAh/g for the pure sample). Concerning the cycling stability, the doped samples were able to provide 129 mAh/g (Mn 10%) and 150 mAh/g (Mn 5%) at C/10 after 60 cycles.

Publisher

MDPI AG

Subject

Electrical and Electronic Engineering,Electrochemistry,Energy Engineering and Power Technology

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