Literature DB >> 30211276

Dataset analysis on Cu9S5 material structure and its electrochemical behavior as anode for sodium-ion batteries.

Mingjun Jing1, Fengliang Long2, Luming Jing3, Xiaopei Lv3, Jiaheng Zhang1, Tianjing Wu1,4.   

Abstract

The data presented in this data article are related to the research article entitled "Facile Synthetic Strategy to Uniform Cu9S5 Embedded into Carbon: A Novel Anode for Sodium-Ion Batteries" (Jing et al., 2018) [1]. The related experiment details of pure Cu9S5 has been stated. The structure data of pure Cu9S5 and the electrochemical performance for sodium-ion batteries are described.

Entities:  

Year:  2018        PMID: 30211276      PMCID: PMC6129733          DOI: 10.1016/j.dib.2018.08.168

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table Value of the data Detailed experimental data might be used in the development of further experiments in a particular area. The summary of material properties can be utilized to compare together and easily accessed from the various applications. The CV curves could be used for more scientific analysis of various metal sulfide as anode for Na-ion batteries.

Data

In this data article, the detailed experimental method of pure Cu9S5 sample has been presented. The X-ray diffraction (XRD) pattern and Cyclic voltammetry (CV) files of as-prepared sample shown in Fig. 1, which is utilized to analysis the electrochemical performance of as-prepared material as anode for sodium-ion batteries.
Fig. 1

(a) XRD pattern of pure Cu9S5. (b) CV files of pure Cu9S5 electrode at 0.2 mV s−1.

(a) XRD pattern of pure Cu9S5. (b) CV files of pure Cu9S5 electrode at 0.2 mV s−1.

Experimental design, materials, and methods

An ethylenediamine-assisted hydrothermal method has been utilized to prepare pure Cu9S5 nanomaterial, according to previous report [2]. The detailed experimental design is as follows. Firstly, 6.0 mL of anhydrous ethylenediamine was dissolved in 24.0 mL deionized water. 1.5 mmol of Cu(NO3)2·6H2O was dissolved the above solution to form a blue solution with ultrasonic dispersion for 10 minutes. And then, 1.5 mmol of thiourea was introduced to the solution in batches, while the above solution is in the process of magnetic stirring. After 30 min, the color of mixture become deep blue. Then, this mixture system was transferred into a 50 mL Teflon-lined stainless steel autoclave and treated at 120 °C for 2 h. Furthermore, black precipitates were deposited on autoclave bottom after the temperature dropping down to room temperature naturally. The pale upper clear liquid was poured out. Then, the black precipitates were washed several times utilizing absolute ethanol and distilled water with (1:1 of the volume ratio). Finally, the products were further dried at 80 °C for 24 h, and the pure Cu9S5 was obtained. X-ray diffraction (XRD) has been utilized to investigate the crystalline structure of pure Cu9S5. The detailed test parameters are based on Ref. [1]. Cyclic voltammetry (CV) tests of pure Cu9S5 has been measured on electrochemical working station (CHI 660B) through assembled CR2025 coin cells utilizing sodium foil as counter and reference electrode, according to previous report [1]. Fig. 1a displays the XRD pattern of as-obtained Cu9S5. The diffraction peaks of material matched well to the pure hexagonal Cu9S5 phase (JCPDS card No. 47–1748). The peaks at 27.7°, 29.2°, 32.3°, 41.5°, 46.3° and 54.9° correspond to the (0 0 15), (1 0 7), (1 0 10), (0 1 17), (1 1 0) and (1 1 15) crystal planes of hexagonal Cu9S5. Furthermore, the CV profiles of Cu9S5 were tested with the potential range from 0.01 to 3.0 V (vs Na/Na+) at 0.2 mV s−1, which is shown in Fig. 1b. In the first cathodic scan, several oxidation peaks take place from 0.2 to 2.0 V, which is mainly attributed to the oxidation reactions of Cu9S5, the insertion process of Na+ into electrode material, and the formation of solid electrolyte interphase (SEI) [1], [3], [4]. During the following anodic scanning, two major peaks at 1.65 and 2.12 V represent the electrochemical reaction from Cu and Na2S to NaαCuβSγ and further changed into Cu9S5 [5]. These obvious redox peaks of pure Cu9S5 are present, illustrating the pure Cu9S5 active material mainly presents conversion reaction in the sodiation/desodiation process. Additionally, the microstructure analysis indicates that Cu9S5 electrode material could also exhibit little insertion/extraction mechanism like other metal sulfides [6], [7].
Subject areaChemistry
More specific subject areaSodium-ion batteries
Type of dataFigure
How data was acquiredX-ray diffraction (XRD, Rigaku D/max 2550 VB+); CHI660B electrochemical analyzer (Shanghai Chenhua Instruments Co., Ltd.).
Data formatAnalyzed
Experimental factorsSamples, assembled coin cells metallic sodium foil as counter and reference electrode
Experimental featuresXRD character of sample and CV performance of electrode material
Data source locationYueyang, China
Data accessibilityThe data is with this article.
Related research article[1] M. Jing, F. Li, M. Chen, J. Zhang, F. Long, L. Jing, X. Lv, T. Wu, X. Ji, Facile synthetic strategy to uniform Cu9S5 embedded into carbon: A novel anode for sodium-ion batteries, J. Alloy. Compd., 762 (2018) 473–479.
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