Effect of Li+ doping on the color performance and temperature stability of γ-Sm2S3

IF 3 4区 材料科学 Q3 CHEMISTRY, PHYSICAL
Haining Wang, Yueming Li, Kai Li, Fusheng Song, Yi Sun, Zhumei Wang
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引用次数: 0

Abstract

Using Sm2O3 as the samarium source, Li2CO3 as the Li+ doping source, and CS2 as the sulfur source, the yellow pigment Li+-doped γ-Sm2S3 was obtained by solid-phase reaction at 900 °C for 120 min. The effects of different molar ratios of Li and Sm (nLi/nSm = 0–0.20) on the phase composition, color state and temperature stability of γ-Sm2S3 were systematically studied. The structure and properties of the pigment were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and differential thermal gravimetric analysis (TG-DTA). The results showed that the pure α-Sm2S3 phase was obtained after vulcanization without adding Li+. When the ratio of nLi/nSm is 0.02–0.06, α phase and γ phase exist simultaneously. When the ratio of nLi/nSm is 0.08–0.20, α phase has been completely transformed to γ phase. With the increase of nLi/nSm, the color of the sample gradually changed from light green to yellow-green and then to yellow. When the ratio of nLi/nSm is 0.14, the yellowness value of the sample b* reached the highest (L* = 63.25, a* = 4.63, b* = 67.26).
Li+掺杂对γ-Sm2S3显色性能和温度稳定性的影响
以Sm2O3为钐源,Li2CO3为Li+掺杂源,CS2为硫源,在900℃固相反应120 min得到Li+掺杂的黄色颜料γ-Sm2S3。系统研究了Li和Sm的不同摩尔比(nLi/nSm = 0-0.20)对γ-Sm2S3的物相组成、色态和温度稳定性的影响。采用x射线衍射(XRD)、扫描电镜(SEM)和差热重分析(TG-DTA)对颜料的结构和性能进行了表征。结果表明:在不添加Li+的情况下,硫化得到了纯净的α-Sm2S3相;当nLi/nSm比为0.02 ~ 0.06时,同时存在α相和γ相。当nLi/nSm比为0.08 ~ 0.20时,α相完全转变为γ相。随着nLi/nSm的增加,样品的颜色逐渐由浅绿色变为黄绿色,再变为黄色。当nLi/nSm为0.14时,样品b*的黄度值最高(L* = 63.25, a* = 4.63, b* = 67.26)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Solid State Ionics
Solid State Ionics 物理-物理:凝聚态物理
CiteScore
6.10
自引率
3.10%
发文量
152
审稿时长
58 days
期刊介绍: This interdisciplinary journal is devoted to the physics, chemistry and materials science of diffusion, mass transport, and reactivity of solids. The major part of each issue is devoted to articles on: (i) physics and chemistry of defects in solids; (ii) reactions in and on solids, e.g. intercalation, corrosion, oxidation, sintering; (iii) ion transport measurements, mechanisms and theory; (iv) solid state electrochemistry; (v) ionically-electronically mixed conducting solids. Related technological applications are also included, provided their characteristics are interpreted in terms of the basic solid state properties. Review papers and relevant symposium proceedings are welcome.
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