Vacancies‐Induced Delocalized States Cobalt Phosphide for Binder‐Free Anode Toward Stable and High‐Rate Sodium‐Ion Batteries

Author:

Zhang Heng1ORCID,Cheng Junquan1,Xia Xin1,Qiu Lang2,Liu Feng1,Sun Wei3,Bai Youcun1,Li Chang Ming1ORCID

Affiliation:

1. School of Materials Science and Engineering Institute of Materials Science and Devices Suzhou University of Science and Technology Suzhou 215009 China

2. School of Chemical Engineering Sichuan University Chengdu 610065 China

3. College of Chemistry and Chemical Engineering Hainan Normal University Haikou 571158 China

Abstract

AbstractMetal phosphides with easy synthesis, controllable morphology, and high capacity are considered as potential anodes for sodium‐ion batteries (SIBs). However, the inherent shortcomings of metal phosphating materials, such as conductivity, kinetics, volume strain, etc are not satisfactory, which hinders their large‐scale application. Here, a CoP@carbon nanofibers‐composite containing rich Co─N─C heterointerface and phosphorus vacancies grown on carbon cloth (CoP1‐x@MEC) is synthesized as SIB anode to accomplish extraordinary capacity and ultra‐long cycle life. The hybrid composite nanoreactor effectively impregnates defective CoP as active reaction center while offering Co─N─C layer to buffer the volume expansion during charge–discharge process. These vast active interfaces, favored electrolyte infiltration, and a well‐structured ion‐electron transport network synergistically improve Na+ storage and electrode kinetics. By virtue of these superiorities, CoP1‐x@MEC binder‐free anode delivers superb SIBs performance including a high areal capacity (2.47 mAh cm−2@0.2 mA cm−2), high rate capability (0.443 mAh cm−2@6 mA cm−2), and long cycling stability (300 cycles without decay), thus holding great promise for inexpensive binder‐free anode‐based SIBs for practical applications.

Publisher

Wiley

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