首页|聚乳酸基硬碳的制备及其电化学性能研究

聚乳酸基硬碳的制备及其电化学性能研究

扫码查看
使用废弃吸管基聚乳酸(PLA)为前驱体,用混合磷酸预氧化交联后进行高温碳化制备了废弃PLA基硬碳.结果表明,碳化温度过低使这种PLA基硬碳的孔隙结构不稳定或稳定性较低;碳化温度过高则使非碳元素流失和可逆比容量降低.P元素的引入使硬碳的层间距达到0.37nm,碳化温度为700℃制备出的废弃PLA基硬碳具有蜂窝状球形框架、较小的比表面积和更丰富的P、O杂原子含量,电流密度为100mA/g时放电比容量为552mAh/g,初始库伦效率为58.7%(324 mAh/g),循环100圈后其循环稳定性仍然较高.经多个电流密度循环后,其可逆放电比容量仍为408 mAh/g.
Preparation and Electrochemical Properties of Discarded Polylactic Acid Hard Carbon
Polylactic acid(PLA)is a widely used biomass-derived polymer material.A significant amount of discarded polylactic acid is generated every year in the disposable product sector.Herein,a discarded PLA-based hard carbon was synthesized with discarded PLA as precursor,through cross-link-ing reaction with phosphoric acid and then followed by high-temperature carbonization.The results indi-cate that excessively lower carbonization temperature will result in unstable pore structure with lower sta-bility.Higher carbonization temperature leads to loss innon-carbon elements and decrease in reversible specific capacity.The introduction of phosphorus(P)increases the spacing between the hard carbon la-mellae to 0.37 nm.At carbonization temperature of 700℃,the prepared discarded PLA-based hard car-bon presents a honeycomb-like spherical framework with smaller specific surface area,and richer in high content of heteroatoms P and O,therefore exhibits the best electrochemical performance.By testing the assembled lithium-ion battery with electrode made of the acquired hard carbon,results show that by a current density of 100 mA/g,the specific capacity can reach 552 mAh/g;while for an initial Coulomb effi-ciency of 58.7%(324 mAh/g),the cycle stability is still excellent after 100 cycles.Besides,after multiple cycles at varying current densities,a reversible discharge capacity of 408 mAh/g is still maintained.

organic polymer materialspolylactic acidhard carbonlithium-ion battery

敖霜霜、徐嘉晨、王宇作、阮殿波、乔志军

展开 >

宁波大学先进储能技术与装备研究院 宁波 315211

有机高分子材料 聚乳酸 硬碳 锂离子电池

2024

材料研究学报
国家自然科学基金委员会 中国材料研究学会

材料研究学报

CSTPCD北大核心
影响因子:0.605
ISSN:1005-3093
年,卷(期):2024.38(11)