Charge Transfer Resistance Between Garnet-Type Solid Electrolyte and Lithium Metal Anode

2018 ◽  
Vol 2 (10) ◽  
pp. 2165-2170 ◽  
Author(s):  
Chengtian Zhou ◽  
Alfred Junio Samson ◽  
Kyle Hofstetter ◽  
Venkataraman Thangadurai

An economical and simple technique to mitigate the solid electrolyte–lithium metal anode interfacial charge transfer resistance.


2016 ◽  
Vol 286 ◽  
pp. 24-33 ◽  
Author(s):  
Sebastian Wenzel ◽  
Dominik A. Weber ◽  
Thomas Leichtweiss ◽  
Martin R. Busche ◽  
Joachim Sann ◽  
...  

2020 ◽  
Vol 10 (27) ◽  
pp. 2000945 ◽  
Author(s):  
Thorben Krauskopf ◽  
Boris Mogwitz ◽  
Hannah Hartmann ◽  
Dheeraj K. Singh ◽  
Wolfgang G. Zeier ◽  
...  

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.


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