Improved Electrochemical Performance and Diffusion kinetics by Boron-doping in Na$_{0.66}$Mn$_{0.8}$Fe$_{0.2}$O$_{2}$ Layered Cathodes for Sodium-Ion Batteries

Fuente: arXiv
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Autori principali: Pati, Jayashree, Senthilkumar, P., Seth, Deepak, Gulati, Riya, Singh, Manish Kr., Sharma, Madhav, Dhaka, Anita, Haider, M. Ali, Dhaka, Rajendra S.
Natura: Preprint
Pubblicazione: 2026
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author Pati, Jayashree
Senthilkumar, P.
Seth, Deepak
Gulati, Riya
Singh, Manish Kr.
Sharma, Madhav
Dhaka, Anita
Haider, M. Ali
Dhaka, Rajendra S.
author_facet Pati, Jayashree
Senthilkumar, P.
Seth, Deepak
Gulati, Riya
Singh, Manish Kr.
Sharma, Madhav
Dhaka, Anita
Haider, M. Ali
Dhaka, Rajendra S.
contents We report the electrochemical investigation and study the diffusion kinetics of boron doped Na$_{0.66}$Mn$_{0.8}$Fe$_{0.2}$O$_{2}$ (B-NMFO) cathode materials for sodium-ion batteries. Notably, the B-NMFO cathode exhibits improved specific capacity of 163 mAh g$^{-1}$ as compared to 133 mAhg$^{-1}$ at 0.1~C for the NMFO cathode. Further, we observe better capacity retention of 70\% for B-NMFO as compared to the NMFO (60\%) at 1 C after 200 cycles, indicating high structural stability due to the presence of strong B-O bonds. The diffusion coefficient evaluation through galvanostatic intermittent titration technique and cyclic voltammetry, which is found to be in the range of 10$^{-8}$--10$^{-10}$ cm$^{2}$s$^{-1}$. Interestingly, the temperature dependent distribution of relaxation time (DRT) analysis provides a clear understanding about the individual physical processes occurring at different time domains during the electro-chemical testing. Moreover, density functional theory is employed to determine the energetics and the electronic properties of B-NMFO, which suggests that the interstitial tetrahedral sites, especially those next to vacancies, are the dominant incorporation path ways for B in the host structure. Additionally, classical molecular dynamics (MD) simulations are applied to gain insights into the Na-ion transport properties in the bulk structures cathode materials.
format Preprint
id arxiv_https___arxiv_org_abs_2604_24683
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Improved Electrochemical Performance and Diffusion kinetics by Boron-doping in Na$_{0.66}$Mn$_{0.8}$Fe$_{0.2}$O$_{2}$ Layered Cathodes for Sodium-Ion Batteries
Pati, Jayashree
Senthilkumar, P.
Seth, Deepak
Gulati, Riya
Singh, Manish Kr.
Sharma, Madhav
Dhaka, Anita
Haider, M. Ali
Dhaka, Rajendra S.
Materials Science
Chemical Physics
We report the electrochemical investigation and study the diffusion kinetics of boron doped Na$_{0.66}$Mn$_{0.8}$Fe$_{0.2}$O$_{2}$ (B-NMFO) cathode materials for sodium-ion batteries. Notably, the B-NMFO cathode exhibits improved specific capacity of 163 mAh g$^{-1}$ as compared to 133 mAhg$^{-1}$ at 0.1~C for the NMFO cathode. Further, we observe better capacity retention of 70\% for B-NMFO as compared to the NMFO (60\%) at 1 C after 200 cycles, indicating high structural stability due to the presence of strong B-O bonds. The diffusion coefficient evaluation through galvanostatic intermittent titration technique and cyclic voltammetry, which is found to be in the range of 10$^{-8}$--10$^{-10}$ cm$^{2}$s$^{-1}$. Interestingly, the temperature dependent distribution of relaxation time (DRT) analysis provides a clear understanding about the individual physical processes occurring at different time domains during the electro-chemical testing. Moreover, density functional theory is employed to determine the energetics and the electronic properties of B-NMFO, which suggests that the interstitial tetrahedral sites, especially those next to vacancies, are the dominant incorporation path ways for B in the host structure. Additionally, classical molecular dynamics (MD) simulations are applied to gain insights into the Na-ion transport properties in the bulk structures cathode materials.
title Improved Electrochemical Performance and Diffusion kinetics by Boron-doping in Na$_{0.66}$Mn$_{0.8}$Fe$_{0.2}$O$_{2}$ Layered Cathodes for Sodium-Ion Batteries
topic Materials Science
Chemical Physics
url https://arxiv.org/abs/2604.24683