globalchange  > 全球变化的国际研究计划
项目编号: 1748363
项目名称:
EAGER: Carbon-Free and Binder-Free Cathode Configurations for High-Energy Lithium-Sulfur Batteries
作者: Leela Arava
承担单位: Wayne State University
批准年: 2017
开始日期: 2017-09-01
结束日期: 2019-02-28
资助金额: 149541
资助来源: US-NSF
项目类别: Standard Grant
国家: US
语种: 英语
特色学科分类: Engineering - Chemical, Bioengineering, Environmental, and Transport Systems
英文关键词: carbon-free electrode configuration ; lithium-sulfur ; intermediate polysulfide ; cathode ; eager project ; promising next-generation energy storage technology ; li/s battery ; solid sulfur ; mobile energy lab program ; renewable energy storage system ; high school student ; high theoretical energy density
英文摘要: Advances in battery technology have been the driving force for the development of new electric vehicles and renewable energy storage systems for the electric grid. New chemistries are needed that are superior to current battery systems for both performance and cost. Among the various alternatives, lithium-sulfur (Li/S) chemistries are the most promising next-generation energy storage technologies, as they lead to advantages such as high theoretical energy density, wide range of operational temperature, and low cost. However, fundamental research is needed on Li/S batteries to address issues including short cycle life, poor coulombic efficiency and self-discharge. The primary goal of this EAGER project is to introduce electrocatalytic porous current collectors in the Li/S battery, which will fundamentally alter electrochemical properties and overcome many current shortcomings. The critical insight gained can be applied to a broad range of materials and energy related research fields such as solar cells, redox flow batteries and fuel cells. The educational and outreach activities associated with the project include active participation of undergraduates from underrepresented groups in the research program and hands-on experiences to high school students through Wayne State's Mobile Energy Lab program.

The goal of this fundamental research project is to address low charging efficiency and short cycle life issues of Li/S batteries. The approach used is to confine the dissolved intermediate polysulfides within the cathode of the cell. The research is based on the hypothesis that the polysulfide-shuttle process in the Li/S cell can be controlled by using electrocatalysis driven kinetics and surface adsorption chemistries. The objective is to confine the dissolved intermediate polysulfides within the cathode of the cell while enhancing the intermediate's utilization and reaction rate using engineered porous catalytic current collectors with the electrocatalysts integrated in it. The PI will investigate the following proposed roles of the electrocatalyst: (i) adsorb dissolved intermediate polysulfides on the catalyst surface to prevent polysulfide shuttle process; (ii) accelerate the reaction kinetics for transforming intermediate polysulfides to lower order polysulfides; and (iii) convert end product of discharge process back to solid sulfur during the charge process to improve cycle life. This EAGER project introduces a new concept of electrocatalytic mitigation that could define a novel pathway towards designing carbon-free electrode configurations with outstanding electrochemical properties.
资源类型: 项目
标识符: http://119.78.100.158/handle/2HF3EXSE/89058
Appears in Collections:全球变化的国际研究计划
科学计划与规划

Files in This Item:

There are no files associated with this item.


Recommended Citation:
Leela Arava. EAGER: Carbon-Free and Binder-Free Cathode Configurations for High-Energy Lithium-Sulfur Batteries. 2017-01-01.
Service
Recommend this item
Sava as my favorate item
Show this item's statistics
Export Endnote File
Google Scholar
Similar articles in Google Scholar
[Leela Arava]'s Articles
百度学术
Similar articles in Baidu Scholar
[Leela Arava]'s Articles
CSDL cross search
Similar articles in CSDL Cross Search
[Leela Arava]‘s Articles
Related Copyright Policies
Null
收藏/分享
所有评论 (0)
暂无评论
 

Items in IR are protected by copyright, with all rights reserved, unless otherwise indicated.