Novel Preoxidation-Assisted Mechanism to Preciously Form and Disperse Bi2O3 Nanodots in Carbon Nanofibers for Ultralong-Life and High-Rate Sodium Storage

材料科学 纳米棒 化学工程 纳米点 静电纺丝 氧化物 煅烧 碳纤维 碳纳米纤维 纳米技术 无机化学 碳纳米管 催化作用 复合材料 复合数 聚合物 有机化学 工程类 化学 冶金
作者
Changmeng Xu,Yu Tian,Jingrui Sun,Mai Li,Wenming Song,Jie You,Min Feng,Xiaojun Wang,Peng Wang,Huifang Li,Guoxin Zhang,Yan He,Zhiming Liu
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (1): 1891-1902 被引量:4
标识
DOI:10.1021/acsami.2c19627
摘要

Metal oxides, as promising electrode materials for sodium-ion batteries, usually need to be formed by exposure to oxygen, which usually thermally corrodes the carbon material with which they are compounded, reducing their flexibility and electrical conductivity. Herein, we present for the first time a preoxidation-assisted mechanism to prepare bismuth oxide and carbon nanofibers (Bi2O3@C-NFs) by electrospinning, using Bi2S3 nanorods as multifunctional templates. The bismuth could be oxidized by C═O bonds formed through the cyclization reaction in the high-temperature calcination process, effectively avoiding thermal corrosion of carbon in oxygen atmosphere at high temperature. More importantly, the uniformly distributed Bi2O3 nanodots and longitudinal tunnels are formed inside the S- and N-doped carbon nanofibers with the continuous diffusion of Bi generated from the decomposition of Bi2S3 nanorods and the conversion to Bi─O bonds with C═O bonds being broken. Benefiting from the structural and composition merits arising from preoxidation, Bi2O3@C-NFs self-supporting anodes show high specific capacity (439 mAh g-1 at 0.05 A g-1), superior rate performance (243 mAh g-1 at a current density of 20 A g-1), and outstanding cycling stability (211 mAh g-1 after 2000 cycles at 5 A g-1). The effective combination of the well-established electrospinning technology and the preoxidation assisted mechanism provides a new way for the preparation of metal oxide and carbon composites.
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