Controlled synthesis of multi-doped highly-disordered porous biomass carbon microsphere for ultra-stable and fast sodium storage

杂原子 阳极 碳纤维 煅烧 材料科学 化学工程 纳米技术 化学 复合材料 电极 工程类 复合数 有机化学 催化作用 冶金 物理化学 戒指(化学)
作者
Xuqiang Hu,Xiaoyu Fan,Zhenkai Mou,Wenpei Kang,Daofeng Sun
出处
期刊:Journal of energy storage [Elsevier BV]
卷期号:83: 110619-110619 被引量:11
标识
DOI:10.1016/j.est.2024.110619
摘要

Biomass-derived hard carbon has been considered as one of the most promising anodes for sodium-ion batteries (SIBs), owing to its natural abundance, sustainability, and in-situ multi-heteroatom doping property. In this work, highly-disordered porous carbon microspheres with in-situ ternary N, P, O-doping (NOP-PCM) are synthesized through a hydrothermal and high-temperature activation process, using porphyra as precursor. Through seriously regulating the calcination temperature and KOH amount, the optimal NOP-PCM-800 can well preserve the microsphere structure, producing abundant pores and defects. Attributed to the porous structure and in-situ heteroatom doping, NOP-PCM-800 can shorten the Na+ transport distance, increase the active sites for the Na+ adsorption and enhance the electron conductivity, leading to enhanced high-rate sodium storage capability. As anode material for sodium ion batteries (SIBs), NOP-PCM-800 can deliver stable capacities of 56.1 mAh g−1 and high capacity retention of 94.4 % at 5.0 A g−1 over 8000 cycles, which is promoted by the enhanced pseudo-capacitive contribution. Based on the ex-situ Raman analysis, the adsorption-intercalation mechanism is responsible for the sodium storage. And in the full cell coupled with Na3V2(PO4)3@C, it can also keep a capacity of 76.9 mAh g−1 at 0.1 A g−1 over 100 cycles, demonstrating its potential practical application.
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