2017
DOI: 10.1016/j.jallcom.2017.01.204
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Enhancing structure integrity and corrosion resistance of Mg alloy by a two-step deposition to avoid F ions etching to nano-SiO2 reinforcement

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Cited by 57 publications
(19 citation statements)
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“…are ascribed to the characteristic diffraction peaks of Mg (PDF 35-0821). These small and weak peaks at 18.59°, 38.02°, 58.64°, and 62.07° are the characteristic peaks of Mg(OH) 2 (PDF 07-0239) [ 19 , 20 ]. The XRD patterns of all coatings are almost identical and two new peaks appear at ca.…”
Section: Resultsmentioning
confidence: 99%
“…are ascribed to the characteristic diffraction peaks of Mg (PDF 35-0821). These small and weak peaks at 18.59°, 38.02°, 58.64°, and 62.07° are the characteristic peaks of Mg(OH) 2 (PDF 07-0239) [ 19 , 20 ]. The XRD patterns of all coatings are almost identical and two new peaks appear at ca.…”
Section: Resultsmentioning
confidence: 99%
“…The lack of a microscale reaction mechanism limits essential understanding of performance and failure models of the LIBs, as well as the optimal design of new materials for the next generation of high-performance LIBs. In terms of the characterization of the morphologies and structural evolution of the LIB electrode materials, many regular analytical and diagnostic techniques in material investigations, such as scanning electron microscopy (SEM) and X-ray diffraction (XRD) in corrosion, [62][63][64] have been adopted in LIB studies. The morphologies can be imaged by SEM, 59,[65][66][67][68][69][70] TEM, [70][71][72][73][74][75][76] and atomic force microscopy (AFM).…”
Section: In Situ Tem and In Situ Tem-electrochemistry Techniquesmentioning
confidence: 99%
“…The typical SEM and TEM micrographs of the MgAl-LDH precipitation are presented in According to results and analyses of the 1 H NMR, 13 C NMR, MS, and FT-IR spectra (given in the Support Information, Figs. S1-S4 and Tables S1-S3), the NTA was synthesized successfully.…”
Section: Resultsmentioning
confidence: 99%
“…3085.21 (cm −1 ), 1640.62 (cm −1 ), 1473.01 (cm −1 ), 1 827.61 (cm −1 ) and other FT-IR peaks indicate that the organic compound has a thiophene ring. Results of binding to 1 H NMR and 13 C NMR spectra: 1 H NMR (ppm): δ 0.91-0.88 (t, 3H), 1.36-1.27 (m, 26H), 1.81 (m, 2H), 3.50-3.46 (t, 2H), 2 13 C NMR (ppm): δ 63.69 31.90, 29.73, 29.67, 29.63, 29.58, 29.53, 29.45, 29.40, 29.34, 29.25, 29.17, 26.30, 22.92, 22.67, 14.14 indicate a C-16 alkyl linear group attached to N; 1 H NMR (ppm): δ 5.13 (s, 2H), 13 C NMR (ppm): δ 61.63 represent a methylene group attached to the N and thiophene ring; 1 H NMR (ppm): δ 7.96-7.95 ( m, 1H), 7.45-7.43 (m, 1H), 7.33-7.32 (m, 1H), 13…”
Section: Resultsmentioning
confidence: 99%
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