多硫化物
硫黄
杂原子
材料科学
X射线光电子能谱
无机化学
化学工程
化学吸附
兴奋剂
表面改性
碳纤维
锂(药物)
电解质
电极
吸附
有机化学
物理化学
化学
复合材料
医学
戒指(化学)
光电子学
复合数
工程类
冶金
内分泌学
作者
Quanquan Pang,Juntao Tang,He Huang,Xiao Liang,Connor J. Hart,Kam Chiu Tam,Linda F. Nazar
标识
DOI:10.1002/adma.201502467
摘要
A sulfur electrode exhibiting strong polysulfide chemisorption using a porous N, S dual-doped carbon is reported. The synergistic functionalization from the N and S heteroatoms dramatically modifies the electron density distribution and leads to much stronger polysulfide binding. X-ray photoelectron spectroscopy studies combined with ab initio calculations reveal strong Li+–N and Sn2−–S interactions. The sulfur electrodes exhibit an ultralow capacity fading of 0.052% per cycle over 1100 cycles. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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