Junjie Shao, Xiaodong Wang, Houhua Ceng, Lan Hu, Zhean Su
{"title":"Rapid Synthesis of Honeycomb-Structured FeP2@NHC for High-Rate and Durable Lithium Storage","authors":"Junjie Shao, Xiaodong Wang, Houhua Ceng, Lan Hu, Zhean Su","doi":"10.3390/en18061358","DOIUrl":null,"url":null,"abstract":"The concurrent preservation of structural integrity and improvement of electrical conductivity in FeP2 anodes presents a persistent challenge. Herein, FeP2 nanoparticles embedded within a 3D N-doped honeycomb-like carbon framework composite (FeP2@NHC) are synthesized through a phosphorization process with a honeycomb-like Fe3C@NHC as a precursor. The in situ incorporation of FeP2 nanoparticles into the 3D carbon matrix effectively restrains the aggregation, pulverization, and stripping of material during cycling, and significantly enhances reaction kinetics and structural stability, achieving a superior electrochemical performance. Specifically, FeP2@NHC electrodes demonstrate remarkable reversible capacity (1433.9 mA h g−1 at 0.1 A g−1), excellent rate-capability (399.9 mA h g−1 at 10 A g−1), and ultra-long cycle life (631.5 mA h g−1 after 1000 cycles at 2 A g−1). Moreover, XRD analysis reveals that iron-rich Fe3C and Fe3O4 precursors can react with NaH2PO2 to form FeP2 and FeP, respectively. This study offers a rational and practical strategy for designing other phosphorus-rich metal phosphide anode materials.","PeriodicalId":11557,"journal":{"name":"Energies","volume":"18 6","pages":"1358-1358"},"PeriodicalIF":3.9000,"publicationDate":"2025-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.mdpi.com/1996-1073/18/6/1358/pdf?version=1741660232","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energies","FirstCategoryId":"0","ListUrlMain":"https://doi.org/10.3390/en18061358","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
The concurrent preservation of structural integrity and improvement of electrical conductivity in FeP2 anodes presents a persistent challenge. Herein, FeP2 nanoparticles embedded within a 3D N-doped honeycomb-like carbon framework composite (FeP2@NHC) are synthesized through a phosphorization process with a honeycomb-like Fe3C@NHC as a precursor. The in situ incorporation of FeP2 nanoparticles into the 3D carbon matrix effectively restrains the aggregation, pulverization, and stripping of material during cycling, and significantly enhances reaction kinetics and structural stability, achieving a superior electrochemical performance. Specifically, FeP2@NHC electrodes demonstrate remarkable reversible capacity (1433.9 mA h g−1 at 0.1 A g−1), excellent rate-capability (399.9 mA h g−1 at 10 A g−1), and ultra-long cycle life (631.5 mA h g−1 after 1000 cycles at 2 A g−1). Moreover, XRD analysis reveals that iron-rich Fe3C and Fe3O4 precursors can react with NaH2PO2 to form FeP2 and FeP, respectively. This study offers a rational and practical strategy for designing other phosphorus-rich metal phosphide anode materials.
同时保持结构完整性和提高FeP2阳极的导电性是一个持续的挑战。本文以蜂窝状Fe3C@NHC为前驱体,通过磷酸化工艺合成了嵌入三维n掺杂的蜂窝状碳骨架复合材料(FeP2@NHC)中的FeP2纳米颗粒。将FeP2纳米颗粒原位掺入三维碳基体中,有效抑制了循环过程中材料的聚集、粉碎和剥离,显著提高了反应动力学和结构稳定性,实现了优异的电化学性能。具体来说,FeP2@NHC电极表现出显著的可逆容量(在0.1 A g−1时为1433.9 mA h g−1),出色的倍率能力(在10 A g−1时为399.9 mA h g−1),超长的循环寿命(在2 A g−1下循环1000次后为631.5 mA h g−1)。XRD分析表明,富铁的Fe3C和Fe3O4前驱体可以分别与NaH2PO2反应生成FeP2和FeP。本研究为其它富磷金属磷化物阳极材料的设计提供了合理实用的策略。
期刊介绍:
Energies (ISSN 1996-1073) is an open access journal of related scientific research, technology development and policy and management studies. It publishes reviews, regular research papers, and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.