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用于高性能锂硫电池中增强多硫化物吸附和转化的氮空位富集多孔氮化硼纤维

N-Vacancy Enriched Porous BN Fibers for Enhanced Polysulfides Adsorption and Conversion in High-Performance Lithium-Sulfur Batteries.

作者信息

Cheng Long, Huang Yang, Ahmad Mehraj, Liu Yue, Xu Jiaqi, Liu Yihong, Seidi Farzad, Wang Dongqing, Lin Zixia, Xiao Huining

机构信息

International Innovation Center for Forest Chemicals & Materials, Jiangsu Co-Innovation Center of Efficient Processing & Utilization of Forest Resources, Nanjing Forestry University, Nanjing, 210037, China.

FAMSUN New Energy BU, Famsun Group Changzhou Huacai New Energy technology Co., Ltd., Changzhou, 100043, China.

出版信息

Chemistry. 2024 Sep 19;30(53):e202402200. doi: 10.1002/chem.202402200. Epub 2024 Sep 3.

Abstract

Severe shuttle effect of soluble polysulfides and sluggish redox kinetics have been thought of as the critical issues hindering the extensive applications of lithium-sulfur batteries (LSBs). Herein, one-dimensional boron nitride (1D BN) fibers with abundant pores and sufficient N-vacancy defects were synthesized using a thermal crystallization following a pre-condensation step. The 1D structure of BN facilitates unblocked ions diffusion pathways during charge/discharge cycles. The embedded pores within the polar BN strengthen the immobilization of polysulfides via both physical confinement and chemical interaction. Moreover, the highly exposed active surface area and intentionally created N-vacancy sites substantially promote reaction kinetics by lowering the energy barriers of the rate-limiting steps. After incorporating with conductive carbon networks and elemental S, the as-prepared S/Nv-BN@CBC cathode of LSBs deliver an initial discharge capacity of up to 1347 mAh g at 200 mA g, while maintaining a low decay rate of 0.03 % per cycle over 1000 cycles at 1600 mA g. This work offers an effective strategy to mitigate the shuttle effect and highlights the significant potential of defect-engineered BN in accelerating the reaction kinetics of LSBs.

摘要

可溶性多硫化物的严重穿梭效应和缓慢的氧化还原动力学被认为是阻碍锂硫电池(LSBs)广泛应用的关键问题。在此,通过预缩合步骤后的热结晶合成了具有丰富孔隙和足够氮空位缺陷的一维氮化硼(1D BN)纤维。BN的一维结构有助于在充放电循环过程中实现畅通无阻的离子扩散途径。极性BN内的嵌入孔隙通过物理限制和化学相互作用增强了对多硫化物的固定。此外,高度暴露的活性表面积和有意制造的氮空位位点通过降低限速步骤的能垒,极大地促进了反应动力学。在与导电碳网络和元素硫结合后,所制备的LSBs的S/Nv-BN@CBC正极在200 mA g下的初始放电容量高达1347 mAh g,同时在1600 mA g下1000次循环中保持每循环0.03%的低衰减率。这项工作提供了一种减轻穿梭效应的有效策略,并突出了缺陷工程化BN在加速LSBs反应动力学方面的巨大潜力。

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