Issue 5, 2025
From the journal:

Chemical Communications

Electrochemically self-driven integration of FeSe/FeS heterostructures for enhanced sodium storage and rapid kinetics†

Hui Li,a   Yanchen Fan,b   Guangshuai Han,c   Xin Zhang,a   Haoxi Ben,d   Claire (Hui) Xiong, ORCID logo *e   Chunrong Ma ORCID logo *df  and  Zhaoying Li ORCID logo *a  

* Corresponding authors

a Power Engineering Major, School of Mechanical and Electrical Engineering, Qingdao University, Qingdao 266071, China
E-mail: zhaoyli@qdu.edu.cn

b PetroChina Shenzhen New Energy Research Institute, Shenzhen, China

c School of Automotive Studies, Tongji University, Shanghai 201804, China

d Key Laboratory of Bio-Fibers and Eco-Textiles, Qingdao University, Qingdao 266071, China

e Micron School of Materials Science and Engineering, Boise State University, Boise, ID 83725, USA
E-mail: clairexiong@boisestate.edu

f College of Textiles & Clothing, Qingdao University, Qingdao 266071, China

Abstract

An in situ electrochemical method is proposed to integrate FeSe/FeS heterostructures into a 3D S-doped carbon framework, enhancing sodium storage capacity and kinetics. Concurrently, both in situ and ex situ techniques are employed to investigate the underlying mechanisms.

Graphical abstract: Electrochemically self-driven integration of FeSe/FeS heterostructures for enhanced sodium storage and rapid kinetics

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Article information

DOI
https://doi.org/10.1039/D4CC05233A
Article type
Communication
Submitted
05 Oct 2024
Accepted
06 Nov 2024
First published
15 Nov 2024

Chem. Commun., 2025,61, 889-892

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Electrochemically self-driven integration of FeSe/FeS heterostructures for enhanced sodium storage and rapid kinetics

H. Li, Y. Fan, G. Han, X. Zhang, H. Ben, C. (. Xiong, C. Ma and Z. Li, Chem. Commun., 2025, 61, 889 DOI: 10.1039/D4CC05233A

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