In situ micelle–template–interface reaction route to CdS nanotubes and nanowires

2002 ◽  
Vol 12 (12) ◽  
pp. 3712-3716 ◽  
Author(s):  
Yujie Xiong ◽  
Yi Xie ◽  
Jun Yang ◽  
Rong Zhang ◽  
Changzheng Wu ◽  
...  
ChemInform ◽  
2010 ◽  
Vol 31 (33) ◽  
pp. no-no
Author(s):  
Jiaxing Huang ◽  
Yi Xie ◽  
Bin Li ◽  
Yu Liu ◽  
Yitai Qian ◽  
...  

2000 ◽  
Vol 12 (11) ◽  
pp. 808-811 ◽  
Author(s):  
J. Huang ◽  
Y. Xie ◽  
B. Li ◽  
Y. Liu ◽  
Y. Qian ◽  
...  

2008 ◽  
Vol 323 (2) ◽  
pp. 365-371 ◽  
Author(s):  
Feng-Qiang Lin ◽  
Wen-Sheng Dong ◽  
Chun-Ling Liu ◽  
Zhaotie Liu ◽  
Mengyuan Li

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Wei Guo ◽  
Wanying Zhang ◽  
Yubing Si ◽  
Donghai Wang ◽  
Yongzhu Fu ◽  
...  

AbstractThe interfacial instability of the lithium-metal anode and shuttling of lithium polysulfides in lithium-sulfur (Li-S) batteries hinder the commercial application. Herein, we report a bifunctional electrolyte additive, i.e., 1,3,5-benzenetrithiol (BTT), which is used to construct solid-electrolyte interfaces (SEIs) on both electrodes from in situ organothiol transformation. BTT reacts with lithium metal to form lithium 1,3,5-benzenetrithiolate depositing on the anode surface, enabling reversible lithium deposition/stripping. BTT also reacts with sulfur to form an oligomer/polymer SEI covering the cathode surface, reducing the dissolution and shuttling of lithium polysulfides. The Li–S cell with BTT delivers a specific discharge capacity of 1,239 mAh g−1 (based on sulfur), and high cycling stability of over 300 cycles at 1C rate. A Li–S pouch cell with BTT is also evaluated to prove the concept. This study constructs an ingenious interface reaction based on bond chemistry, aiming to solve the inherent problems of Li–S batteries.


2008 ◽  
Vol 47 (2) ◽  
pp. 723-728 ◽  
Author(s):  
Guozhu Chen ◽  
Caixia Xu ◽  
Xinyu Song ◽  
Wei Zhao ◽  
Yi Ding ◽  
...  

1981 ◽  
Vol 10 ◽  
Author(s):  
J. M. Vandenberg ◽  
F. J. A. Den Broeder ◽  
R. A. Hamm

An in situ annealing X-ray study was applied to Cu-Al thin film couples over a wide range of copper-to-aluminum film ratios. This new technique, which has been previously described for a study on the Au-Al thin film system, enables us to make a temperature-dependent photographic X-ray analysis. The present study indicated that only a limited number of the wide variety of bulk phases form in the Cu-Al thin film interface, while some of these phases in the interface are transient. In the transient stages of the interface reaction, the f.c.c.-ordered phase β-Cu3A1 grows over the entire range of copper-to-aluminum film ratios after the first nucleation of CuA12, indicating a two-step nucleation reaction. On the aluminum-rich side, this phase transforms to a new ordered hexagonal phase β′. It could be interpreted as a superlattice of the metastable hexagonal ω phase occurring in zirconium-based alloys. The end phases are CuA1 and CuAl2.


2010 ◽  
Vol 64 (6) ◽  
pp. 746-748 ◽  
Author(s):  
Denghui Jiang ◽  
Yida Deng ◽  
Haoran Wang ◽  
Bin Shen ◽  
Yating Wu ◽  
...  

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