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深入了解硼掺杂对锂硫电池中硫/碳正极的影响。

Insight into the effect of boron doping on sulfur/carbon cathode in lithium-sulfur batteries.

作者信息

Yang Chun-Peng, Yin Ya-Xia, Ye Huan, Jiang Ke-Cheng, Zhang Juan, Guo Yu-Guo

机构信息

CAS Key Laboratory of Molecular Nanostructure and Nanotechnology and Beijing National Laboratory for Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences (CAS) , Beijing 100190, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2014 Jun 11;6(11):8789-95. doi: 10.1021/am501627f. Epub 2014 Apr 24.

DOI:10.1021/am501627f
PMID:24764111
Abstract

To exploit the high energy density of lithium-sulfur batteries, porous carbon materials have been widely used as the host materials of the S cathode. Current studies about carbon hosts are more frequently focused on the design of carbon structures rather than modification of its properties. In this study, we use boron-doped porous carbon materials as the host material of the S cathode to get an insightful investigation of the effect of B dopant on the S/C cathode. Powder electronic conductivity shows that the B-doped carbon materials exhibit higher conductivity than the pure analogous porous carbon. Moreover, by X-ray photoelectron spectroscopy, we prove that doping with B leads to a positively polarized surface of carbon substrates and allows chemisorption of S and its polysulfides. Thus, the B-doped carbons can ensure a more stable S/C cathode with satisfactory conductivity, which is demonstrated by the electrochemical performance evaluation. The S/B-doped carbon cathode was found to deliver much higher initial capacity (1300 mA h g(-1) at 0.25 C), improved cyclic stability, and rate capability when compared with the cathode based on pure porous carbon. Electrochemical impedance spectra also indicate the low resistance of the S/B-doped C cathode and the chemisorption of polysulfide anions because of the presence of B. These features of B doping can play the positive role in the electrochemical performance of S cathodes and help to build better Li-S batteries.

摘要

为了利用锂硫电池的高能量密度,多孔碳材料已被广泛用作硫阴极的主体材料。目前关于碳主体的研究更多地集中在碳结构的设计上,而非其性能的改性。在本研究中,我们使用硼掺杂的多孔碳材料作为硫阴极的主体材料,以深入研究硼掺杂剂对硫/碳阴极的影响。粉末电子电导率表明,硼掺杂的碳材料比纯类似多孔碳具有更高的电导率。此外,通过X射线光电子能谱,我们证明硼掺杂导致碳基底表面带正电,并允许硫及其多硫化物的化学吸附。因此,硼掺杂的碳可以确保具有令人满意电导率的更稳定的硫/碳阴极,这在电化学性能评估中得到了证明。与基于纯多孔碳的阴极相比,发现硫/硼掺杂碳阴极具有更高的初始容量(在0.25 C时为1300 mA h g(-1))、更好的循环稳定性和倍率性能。电化学阻抗谱也表明硫/硼掺杂碳阴极的电阻较低,并且由于硼的存在导致多硫阴离子的化学吸附。硼掺杂的这些特性可以在硫阴极的电化学性能中发挥积极作用,并有助于构建更好的锂硫电池。

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