硫黄
材料科学
纤维素
氮气
对偶(语法数字)
无机化学
兴奋剂
碳纤维
锂(药物)
有机化学
化学
复合材料
艺术
冶金
内分泌学
文学类
复合数
医学
光电子学
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 Sn (2-) -S interactions. The sulfur electrodes exhibit an ultralow capacity fading of 0.052% per cycle over 1100 cycles.
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