CAS OpenIR
Sulfur-based redox chemistry for electrochemical energy storage
Huang, Xia1,2; Luo, Bin1,2; Chen, Peng1,2; Searles, Debra J.3,4; Wang, Dan5; Wang, Lianzhou1,2
2020-11-01
Source PublicationCOORDINATION CHEMISTRY REVIEWS
ISSN0010-8545
Volume422Pages:26
AbstractThe burgeoning developments of portable electronics and electric vehicles call for continual improvement of electrochemical energy storage technologies. Owing to their rich abundance and versatile oxidation states, various sulfur species (such as molecular sulfur, metal sulfides, metal polysulfides, and polymerised sulfur species) have been studied in a wide spectrum of energy storage systems. In this review, sulfur-based redox chemistries for electrochemical energy storage are coherently analysed, covering the redox mechanism of processes based on conversion, intercalation/deintercalation, cleavage/formation of S-S bonds and combinations of them. Instead of updating the advances of a specific battery system or material, this review focuses on a comprehensive framework for sulfur-based redox chemistries in electrochemical energy storage. Innovative ideas may arise by sharing learning between related areas. (C) 2020 Elsevier B.V. All rights reserved.
KeywordElectrochemical energy storage Anionic redox Cationic redox Sulfur Metal (poly)sulfides Polymerized sulfur
DOI10.1016/j.ccr.2020.213445
Language英语
WOS KeywordALL-SOLID-STATE ; LITHIUM-SULFUR ; LI-S ; CATHODE MATERIAL ; ELECTRODE MATERIALS ; ELEMENTAL SULFUR ; ANIONIC REDOX ; HIGH-CAPACITY ; POLYMERIZATION ELECTRODES ; RECHARGEABLE BATTERIES
Funding ProjectAustralian Research Council ; Queensland-Chinese Academy of Sciences (Q-CAS) Collaborative Science Fund ; National Natural Science Foundation of China[21820102002] ; Taishan Scholar Advantage and Characteristic Discipline Team of Eco Chemical Process and Technology at Qingdao University of Science and Technology, China
WOS Research AreaChemistry
WOS SubjectChemistry, Inorganic & Nuclear
Funding OrganizationAustralian Research Council ; Queensland-Chinese Academy of Sciences (Q-CAS) Collaborative Science Fund ; National Natural Science Foundation of China ; Taishan Scholar Advantage and Characteristic Discipline Team of Eco Chemical Process and Technology at Qingdao University of Science and Technology, China
WOS IDWOS:000558026500010
PublisherELSEVIER SCIENCE SA
Citation statistics
Document Type期刊论文
Identifierhttp://ir.ipe.ac.cn/handle/122111/41648
Collection中国科学院过程工程研究所
Corresponding AuthorLuo, Bin; Wang, Dan; Wang, Lianzhou
Affiliation1.Univ Queensland, Nanomat Ctr, Sch Chem Engn, St Lucia, Qld 4072, Australia
2.Univ Queensland, Australian Inst Bioengn & Nanotechnol, St Lucia, Qld 4072, Australia
3.Univ Queensland, Ctr Theoret & Computat Mol Sci, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
4.Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld 4072, Australia
5.Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, 1 Beiertiao, Beijing 100190, Peoples R China
Recommended Citation
GB/T 7714
Huang, Xia,Luo, Bin,Chen, Peng,et al. Sulfur-based redox chemistry for electrochemical energy storage[J]. COORDINATION CHEMISTRY REVIEWS,2020,422:26.
APA Huang, Xia,Luo, Bin,Chen, Peng,Searles, Debra J.,Wang, Dan,&Wang, Lianzhou.(2020).Sulfur-based redox chemistry for electrochemical energy storage.COORDINATION CHEMISTRY REVIEWS,422,26.
MLA Huang, Xia,et al."Sulfur-based redox chemistry for electrochemical energy storage".COORDINATION CHEMISTRY REVIEWS 422(2020):26.
Files in This Item:
There are no files associated with this item.
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Huang, Xia]'s Articles
[Luo, Bin]'s Articles
[Chen, Peng]'s Articles
Baidu academic
Similar articles in Baidu academic
[Huang, Xia]'s Articles
[Luo, Bin]'s Articles
[Chen, Peng]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Huang, Xia]'s Articles
[Luo, Bin]'s Articles
[Chen, Peng]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

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