![Show Menu](styles/mobile-menu.png)
![Page Background](./../common/page-substrates/page0022.png)
Page 64
conferenceseries
.com
Volume 7
Biosensors Journal
ISSN: 2090-4967
Electrochemistry 2018
June 11-12, 2018
June 11-12, 2018 | Rome, Italy
4
th
International Conference on
Electrochemistry
Surface chemistry and electrode design for high performance Li-S battery
Wen Liu
1
, Cejun Hu
1
, Jijin Yang
1
, Qian Wang
2
, Kai Wu
2
and
Xiaoming Sun
1
1
Beijing University of Chemical Technology, China
2
Peking University, China
B
ased on the reaction of 16Li+S
8
8Li
2
S, Li-S battery reaches a high theoretical energy density of 2600 Wh/kg, which is
several times higher than that of traditional lithium ion batteries (LIBs). The low cost, high capacity as well as environment-
benignity makes Li-S battery as a strong candidate for next generation energy storage. However, the development of Li-S
battery is severely hindered by several problems, including the low conductivity of sulfur cathode, volume variation during
charge/discharge and dissolution of lithium polysulfide (LiPS). These drawbacks cause low utilization of sulfur and poor
cycling performance of batteries. To overcome these obstacles, researchers pay attention to regulating the construction of
sulfur cathode, using mesoporous materials, core-shell types carbon and graphene oxide etc. The carbon based materials have
significant benefit on the conductivity of the electrode and suppress the polysulfide dissolution to some extent. But the nonpolar
carbon intrinsically has poor interaction with LiPS and lithium sulfide. Moreover, the lithium dendrite growth and electrode
pulverization during cycling gives rise to lower columbic efficiency and safety risks. Hence, the polysulfide trapping chemistry,
sulfur electrode design and Li mental electrode protection are the key factors contributing to the cycling performance and
stability of Li-S battery. Herein, we propose polar materials including inorganic mental oxides, metal phosphides and organic
functional groups, which further hybrid with nano carbons to construct bifunctional host for sulfur electrode. On one hand,
the polar sites can strongly absorb LiPS, so that the dissolution of LiPS and shuttling effect can be reduced. On the other hand,
polysulfide after absorption can quickly reacted with electrons and Li-ions, therefore improving the reaction kinetics and
eliminating the bulky dead sulfur formation. Consequently, the Li-S batteries with the high performance sulfur electrodes
can stably run for over 1000 cycles. The mechanism of sulfur trapping chemistry was also revealed by x-ray photoelectron
spectroscopy (XPS) characterization and theoretical calculation. In terms of Li metal anode, the huge volume variation during
cycling cause electrode pulverization, which is especially serious when paired with high mass loading sulfur cathode. We
demonstrate that nanostructuring is one of the key points to realize stable lithium metal anode. Different kinds of scaffold
have been constructed with Li mental to reduce the volume variation and suppress dendrite growth. The lithiophilic treatment
of scaffold leads to lithium uniformly deposit and nucleate on electrode surface. The dendrite-free lithium deposition also
achieved throughmanipulation of Li-ions transport number by modifying a separator withmetal–organic frameworkmaterials
(MOFs).
Recent Publications
1. C Milroy and A Manthiram (2016) Adv. Mater., 28.
2. Y Y Mi, W Liu, K R Yang, J Jiang, Q Fan, Z Weng, Y R Zhong, Z S Wu, G W Brudvig, V S Batista, H H Zhou and H L
Wang (2016) Angew. Chem. Int. Ed., 55:14818-14822.
3. W Liu, J Jiang, Y Y Mi, K Yang, Z Weng, Q Fan, V S Batista, G Brudvig and H L Wang (2017), DOI: 10.1073/
pnas.1620809114.
4. Y Zhong, K R Yang, W Liu, P He, V S Batista and H L Wang (2017) J. Phys. Chem. C, 121:14222-14227.
5. W Liu, Z Weng, Y Y Mi and H L Wang (2017) Chem. Sci. 8:4285-4291.
Biography
Wen Liu has completed his studies at Beijing University of Chemical Technology, China.
liuwen-03721@163.comWen Liu et al., Biosens J 2018, Volume 7
DOI: 10.4172/2090-4967-C1-002