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mxene academic
position: home > mxene academic > mxene energy storage

3D SnS / MXene enhances sodium storage capacity

source:beike new material Views:3306time:2020-08-10 QQ Academic Group: 1092348845

已传文件:photo/2020541037333.png

【Research Background】

Among metal sulfide anodes, tin (II) sulfide has a higher theoretical capacity (1022 mAh g -1 ), which makes it a potential candidate for sodium ion batteries (SIB). The orthorhombic-SnS can store Na + through a combination of transformation and alloying reaction mechanisms , involving two structural phase transitions from orthorhombic-SnS to cubic- Sn to orthorhombic-Na 15 Sn 4 . The controllable size of nano-tin coupled to the surface of the highly conductive substrate can introduce additional pseudocapacitance to maximize the reaction sites on the surface. The ideal two-dimensional (2D) heterostructure has atomic layer thickness, high surface exposure and a large number of edge sites, with enhanced pseudocapacitance and ultrafast dynamics. However, most SnS nanocomposites are mainly concentrated on graphene-based materials. Exploring new strategies to combine with other promising conductive substrates to achieve controllable fabrication of SnS remains a huge challenge.


【Achievement Introduction】

Recently, the Department of Chemistry, Beijing Institute of Technology Minhua Cao professor research group at the internationally renowned academic journal Chemistry - A European Journal published an article entitled: Toward Understanding pseudocapacitive at The Enhanced Storage in 3D SnS / MXene Architecture Enabled by Engineered Surface Reactions research papers , This study developed a precursor-oriented strategy to obtain 3D SnS / Ti 3 C 2 T x hybrids (expressed as SnS / Ti 3 C 2 T x -O) with excellent Na storage , ie in Ti 3 The surface of the tin hydroxide (Sn 6 O 4 (OH) 4 ) precursor on the 2 T x nanosheet was grown, then vulcanized in an oil bath, and then annealed. Compared with one-step hydrothermal vulcanization, precursor-guided vulcanization is achieved under mild conditions. The tiny SnS nanocrystals (about 5 nm in size) formed through a strong TiS covalent bond with the wrinkled Ti 32 T x nanosheets are coupled, exposing a large number of edges and active sites. Our SnS / Ti 3 C 2 T x -O negative electrode has a highly tortuous sheet structure, and has a strong 3D network architecture and a designed surface reaction, which can provide pseudocapacitor-based storage in the SIB, significantly improved a capacity G 0.1 -1 when G mAh 565 -1 and excellent rate performance.


【Graphic introduction】

Flowchart 1.  Schematic diagram of the preparation of 3D SnS / Ti 3 C 2 T x -O and bulk SnS / Ti 3 C 2 T x -H

Figure 1 (a) TEM image of the original Ti 3 C 2 T x nanosheet (b) Sn 6 O 4 (OH) 4  / Ti 3 C 2 T x precursor (c, d) 3D SnS / Ti 3 C 2 T SEM images of x -O and (e, f) bulk SnS / Ti 3 C 2 T x -H

Fig of SnS 2 / of Ti . 3 C 2 T X  -O of (a, b) TEM (c ) HRTEM image (d) EDS spectrum and (e) corresponding to the element mapping images (F) of SnS / of Ti . 3 C 2 T X  -O , SnS / Ti 3 C 2 T x  -H and Ti 3 C 2 T x nitrogen adsorption-desorption isotherms and corresponding pore size distribution (inset)

Figure 3 Physical characterization of SnS / Ti 3 C 2 T x  -O, SnS / Ti 3 C 2 T x  -H and Ti 3 C 2 T x samples

Figure 4 (ac) XANES spectra and related calculations of SnS / Ti 3 C 2 T x -O, SnS / Ti 3 C 2 T x -H and Ti 3 C 2 T x samples (d) SnS / Ti 3 C 2 T X  -O, of SnS / of Ti . 3 C 2 T X  -H, SnCl2 2 ∙ 2H 2 O and SnCl2 . 4 ∙ 5H 2 O in L of Sn . 3 - an edge of the XANES spectrum

Figure 5  Electrochemical performance of SnS / Ti 3 C 2 T x -O electrode

Fig.6  Ectopic XRD pattern of SnS / Ti 3 C 2 T x -O electrode in different states

Fig. 7 Kinetic analysis of the electrochemical behavior of SnS / Ti 3 C 2 T x -O


【Summary of this article】

This article explores a precursor-guided synthesis strategy for the construction of tiny SnS nanocrystals (approximately 5 nm in size) anchored on wrinkled Ti 3 C 2 T x nanosheets. And in SnS / of Ti . 3 C 2 T X of Ti is -H . 3 C 2 T X cover plate on the opposite SnS random, prepared SnS / of Ti . 3 C 2 T X -O ensures powerful 3D network architecture. XPS and EXAFS confirmed the unique Ti-S covalent bond of these two compounds, greatly enhancing the structural durability. In addition, the highly exposed surfaces and edges of SnS nanocrystallites on wrinkled Ti 3 C 2 T x promote ion conduction and reaction kinetics. By greatly improving the surface reaction, the SnS / Ti 3 C 2 T x -O of 1.0 mV s -1 can achieve up to 92.7% of the main contribution of the pseudo-capacitance. Overall, combining the advantages of morphology and structural features, SnS / Ti 3 C 2The T x -O negative electrode improves the Na storage performance as a whole. This work will open up a new way to control the sulfide morphology and nano / microstructure adjustment to achieve excellent electrochemical performance.


Literature link:

https://doi.org/10.1002/chem.202000795

Source: MXene Frontier

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   It is purely academic and non-commercial. If there is any infringement, please contact us immediately. We will delete it as soon as possible to protect the intellectual property of the original author. Thank you teachers and students for your attention and support.



 

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