Binding MoSe2 with dual protection carbon for high-performance sodium storage. Issue 40 (19th August 2019)

• Record Type: Journal Article
• Authors: Su, Qiong; Cao, Xinxin; Yu, Ting; Kong, Xiangzhong; Wang, Yaping; Chen, Jing; Lin, Jiande; Xie, Xuefang; Liang, Shuquan; Pan, Anqiang
• Is Part Of: Journal of materials chemistry. Volume 7:Issue 40(2019)
• Page Start: 22871
• Page End: 22878
• Publication Date: 2019-08-19
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c9ta06870h
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Dual carbon-protected MoSe2 nanorods can enable controlled volume fluctuation, permit continuous electron transfer, and offer more active sites and good redox reversibility. Abstract : Molybdenum selenide (MoSe2 ), a promising anode material for sodium ion batteries (SIBs), has generated intensive scientific interest due to its high theoretical capacity and favorable conversion kinetics. Nevertheless, its practical applications are seriously restricted by the volume variation, inferior structural stability and dissolved poly-selenides. Herein, we report dual carbon protected MoSe2 (MoSe2 @NC@rGO) and the intrinsic mechanism for its enhanced sodium storage performance. Organic–inorganic hybrid Mo3 O10 (C2 H10 N2 ) (MoO x -EDA) is used as a self-sacrificing precursor. The synthesis process involves self-assembly of MoO x -EDA with functionalized graphene oxide (GO) and subsequent thermal selenization. The dual protection carbon layers can block the poly-selenide shuttling, promote electron transfer and buffer the huge volume change. When evaluated as an anode material for SIBs, the optimized MoSe2 @NC@rGO-200 electrode delivers a high reversible specific capacity of 447 mA h g −1 at 100 mA g −1 and maintains an appreciable capacity of 281 mA h g −1 at 5 A g −1 . Moreover, a capacity of 360 mA h g −1 is retained after 200 cycles at 1 A g −1 with no obvious capacity decay. A full-battery configuration coupled with the Na3 V2 (PO4 )2 /C cathode exhibits an average operating potential of 1.8 V and good cycling performance. Such a dual carbon-confined approach can also be extended to other electrode materials with large volume swelling.