{"title":"用于稳定和高倍率钠离子电池的生物质衍生掺磷多孔硬碳阳极","authors":"Puwu Liang, Zijing Huo, Yangjie Liu, Zheng Bo, Yongmin Wu, Xiang Hu, Zhenhai Wen","doi":"10.1002/batt.202400694","DOIUrl":null,"url":null,"abstract":"<p>Biomass-derived hard carbon, despite being promising for anode material of sodium-ion batteries, usually suffer from low initial coulombic efficiency (ICE), poor rate capacity, and limited cycling stability caused by complex surface defects and low intrinsic conductivity. Herein, phosphorus-doped porous hard carbon (HC@PC−P) were synthesized by the thermal polymerization of soy lecithin on the surfaces of hard carbon derived from olive kernels. The incorporation of heteroatom phosphorus in the porous hard carbon framework expands the carbon lattice spacing, optimizes the graphitization degree, and increases electrical conductivity, guaranteeing ensuring rapid electron and ion transfer. These coupling effects enable HC@PC−P anode to achieve a high reversible capacity of 350 mAh g<sup>−1</sup> at 0.1 A g<sup>−1</sup>, an impressive initial coulombic efficiency of 89.6 %, and remarkable long-term cycling stability at 1 A g<sup>−1</sup> over 1000 cycles with negligible capacity fade. The mechanisms behind sodium storage and enhanced electrochemical performance were elucidated by ex-situ Raman spectroscopy and kinetic analysis. Additionally, the assembled HC@PC−P//Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> full cell demonstrated a high energy density of 257.9 Wh kg<sup>−1</sup>. This work provides a rational guide for designing advanced hard carbon anode materials for high-energy sodium-ion batteries.</p>","PeriodicalId":132,"journal":{"name":"Batteries & Supercaps","volume":"8 6","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biomass-Derived Phosphorus-Doped Porous Hard Carbon Anode for Stable and High-Rate Sodium Ion Batteries\",\"authors\":\"Puwu Liang, Zijing Huo, Yangjie Liu, Zheng Bo, Yongmin Wu, Xiang Hu, Zhenhai Wen\",\"doi\":\"10.1002/batt.202400694\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Biomass-derived hard carbon, despite being promising for anode material of sodium-ion batteries, usually suffer from low initial coulombic efficiency (ICE), poor rate capacity, and limited cycling stability caused by complex surface defects and low intrinsic conductivity. Herein, phosphorus-doped porous hard carbon (HC@PC−P) were synthesized by the thermal polymerization of soy lecithin on the surfaces of hard carbon derived from olive kernels. The incorporation of heteroatom phosphorus in the porous hard carbon framework expands the carbon lattice spacing, optimizes the graphitization degree, and increases electrical conductivity, guaranteeing ensuring rapid electron and ion transfer. These coupling effects enable HC@PC−P anode to achieve a high reversible capacity of 350 mAh g<sup>−1</sup> at 0.1 A g<sup>−1</sup>, an impressive initial coulombic efficiency of 89.6 %, and remarkable long-term cycling stability at 1 A g<sup>−1</sup> over 1000 cycles with negligible capacity fade. The mechanisms behind sodium storage and enhanced electrochemical performance were elucidated by ex-situ Raman spectroscopy and kinetic analysis. Additionally, the assembled HC@PC−P//Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> full cell demonstrated a high energy density of 257.9 Wh kg<sup>−1</sup>. This work provides a rational guide for designing advanced hard carbon anode materials for high-energy sodium-ion batteries.</p>\",\"PeriodicalId\":132,\"journal\":{\"name\":\"Batteries & Supercaps\",\"volume\":\"8 6\",\"pages\":\"\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Batteries & Supercaps\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/batt.202400694\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Batteries & Supercaps","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/batt.202400694","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
摘要
生物质硬碳作为钠离子电池的负极材料,具有广阔的应用前景,但由于其表面缺陷复杂,固有电导率低,存在初始库仑效率低、倍率容量差、循环稳定性受限等问题。本文采用大豆卵磷脂在橄榄核硬碳表面热聚合的方法合成了掺磷多孔硬碳(HC@PC−P)。杂原子磷在多孔硬碳骨架中的掺入扩大了碳晶格间距,优化了石墨化程度,提高了电导率,保证了电子和离子的快速转移。这些耦合效应使HC@PC−P阳极在0.1 a g−1下获得350 mAh g−1的高可逆容量,令人印象深刻的初始库仑效率为89.6%,并且在1 a g−1下超过1000次循环时具有显着的长期循环稳定性,容量衰减可以忽略。通过非原位拉曼光谱和动力学分析阐明了钠储存和电化学性能增强的机理。此外,组装的HC@PC−P//Na3V2(PO4)3充满电池的能量密度高达257.9 Wh kg−1。该工作为高能钠离子电池先进硬碳负极材料的设计提供了合理的指导。
Biomass-Derived Phosphorus-Doped Porous Hard Carbon Anode for Stable and High-Rate Sodium Ion Batteries
Biomass-derived hard carbon, despite being promising for anode material of sodium-ion batteries, usually suffer from low initial coulombic efficiency (ICE), poor rate capacity, and limited cycling stability caused by complex surface defects and low intrinsic conductivity. Herein, phosphorus-doped porous hard carbon (HC@PC−P) were synthesized by the thermal polymerization of soy lecithin on the surfaces of hard carbon derived from olive kernels. The incorporation of heteroatom phosphorus in the porous hard carbon framework expands the carbon lattice spacing, optimizes the graphitization degree, and increases electrical conductivity, guaranteeing ensuring rapid electron and ion transfer. These coupling effects enable HC@PC−P anode to achieve a high reversible capacity of 350 mAh g−1 at 0.1 A g−1, an impressive initial coulombic efficiency of 89.6 %, and remarkable long-term cycling stability at 1 A g−1 over 1000 cycles with negligible capacity fade. The mechanisms behind sodium storage and enhanced electrochemical performance were elucidated by ex-situ Raman spectroscopy and kinetic analysis. Additionally, the assembled HC@PC−P//Na3V2(PO4)3 full cell demonstrated a high energy density of 257.9 Wh kg−1. This work provides a rational guide for designing advanced hard carbon anode materials for high-energy sodium-ion batteries.
期刊介绍:
Electrochemical energy storage devices play a transformative role in our societies. They have allowed the emergence of portable electronics devices, have triggered the resurgence of electric transportation and constitute key components in smart power grids. Batteries & Supercaps publishes international high-impact experimental and theoretical research on the fundamentals and applications of electrochemical energy storage. We support the scientific community to advance energy efficiency and sustainability.