High-Capacity and Stable Sodium-Sulfur Battery Enabled by Confined Electrocatalytic Polysulfides Full Conversion

被引:51
作者
Huang, Zhanpeng [1 ]
Song, Bin [2 ]
Zhang, Hong [3 ]
Feng, Fan [3 ]
Zhang, Wenli [4 ]
Lu, Ke [1 ]
Chen, Qianwang [1 ,5 ,6 ]
机构
[1] Anhui Univ, Inst Phys Sci & Informat Technol, Key Lab Struct & Funct Regulat Hybrid Mat, Minist Educ, Hefei 230601, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Suzhou Nano Sci & Technol, Inst Funct Nano & Soft Mat FUNSOM, Lab Nanoscale Biochem Anal, Suzhou 215123, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[4] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou Key Lab Clean Transportat Energy Chem, Guangzhou 510006, Peoples R China
[5] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[6] Univ Sci & Technol China, Dept Mat Sci & Engn, Hefei 230026, Peoples R China
关键词
confined electrocatalysis; core‐ shell structures; Na;  S batteries; polysulfide manipulation; reaction kinetics; PERFORMANCE; CHALLENGES; ELECTRODES;
D O I
10.1002/adfm.202100666
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The efficient polysulfide capture and reversible sulfur recovery during reverse charging process are critical to exploiting the full potential of room temperature Na-S batteries. Here, based on a core-shell design strategy, the structural and chemical synergistic manipulation of sodium polysulfides quasi-solid-state reversible conversion is proposed. The sulfur is encapsulated in the multi-pores of 3D interconnected carbon fiber as the core structure. The Fe(CN)(6)(4-)-doped polypyrrole film serves as a redox-active polar shell to lock up polysulfides and promote complete polysulfide conversion. Importantly, the short-chain Na2S4 polysulfides are reduced to Na2S directly leaving with a small fraction of soluble intermediates as the cation-transfer medium at the core/shell interface, and freeing up formation of solid Na2S2 incomplete product. Further, the redox mediator with open Fe species electrocatalytically lowers the Na2S oxidation energy barrier and renders the high reversibility of electrodeposited Na2S. The tunable quasi-solid-state reversible sulfur conversion under versatile polymer sheath greatly enhances sulfur utilization, affording a remarkable capacity of 1071 mAh g(-1) and a stable high capacity of 700 mAh g(-1) at 200 mA g(-1) after 200 cycles. The confined electrocatalytic effect provides a strategy for tuning electrochemical pathway of sulfur species and guarantees high-efficiency sulfur electrochemistry.
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页数:8
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