BaTiF6:Mn4+bifunctional microstructures with photoluminescence and photocatalysis: hydrothermal synthesis and controlled morphology

光催化 热液循环 发光 材料科学 双功能 光致发光 Crystal(编程语言) 热稳定性 水热合成 晶体结构 纳米技术 化学工程 分析化学(期刊) 矿物学 光电子学 结晶学 化学 催化作用 有机化学 冶金 工程类 计算机科学 程序设计语言
作者
Xiaoli Gao,Yan Song,Guixia Liu,Xiangting Dong,Jinxian Wang,Wensheng Yu
出处
期刊:CrystEngComm [Royal Society of Chemistry]
卷期号:18 (31): 5842-5851 被引量:42
标识
DOI:10.1039/c6ce01046f
摘要

A series of BaTiF6:Mn4+ samples were synthesized via a facile hydrothermal route. The crystal structure and morphology of the obtained products were studied. Detailed investigations indicated that morphologies of bundle-like, microrod, and flower-like structures could be observed by varying the hydrothermal reaction time. Simultaneously, we investigated the influences of the reaction temperature and the barium source on the crystal phases and morphology of the prepared BaTiF6:Mn4+ products. The luminescence properties of the as-synthesized samples were systematically evaluated. The results clearly demonstrated that two intense excitation bands could be observed in the near-UV and the blue region, suggesting that the BaTiF6:Mn4+ samples provide a great opportunity for application in light-emitting diodes (LED) with blue-chip excitation. The prepared BaTiF6:Mn4+ samples exhibited an intense red emission under 470 nm light excitation. Additionally, the changes of the Mn4+ emissions based on different reaction temperatures and barium sources were studied in detail. Temperature-dependent luminescence experiments were also performed in order to evaluate the thermal stability of the BaTiF6:Mn4+ samples. Furthermore, a thorough study of the photocatalytic activities of the as-prepared samples demonstrated that BaTiF6:Mn4+ could promote satisfactory photocatalytic activities.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
zzzzzz完成签到,获得积分10
1秒前
华仔应助我不221采纳,获得10
1秒前
上官若男应助西瓜瓜采纳,获得10
1秒前
3秒前
还没想好发布了新的文献求助30
5秒前
7秒前
7秒前
elang完成签到,获得积分10
8秒前
甜美黄豆发布了新的文献求助10
8秒前
9秒前
一念完成签到,获得积分10
9秒前
10秒前
10秒前
10秒前
10秒前
dew应助皮卡第的玫瑰采纳,获得50
13秒前
13秒前
阿柒发布了新的文献求助10
13秒前
13秒前
阳光绿海完成签到,获得积分10
14秒前
14秒前
犹豫电话完成签到,获得积分20
15秒前
lai发布了新的文献求助10
15秒前
Zhu XY.发布了新的文献求助10
15秒前
16秒前
16秒前
17秒前
wyq123发布了新的文献求助10
18秒前
18秒前
ccc发布了新的文献求助10
20秒前
852应助LALA采纳,获得10
20秒前
星辰大海应助犹豫电话采纳,获得10
20秒前
彭于晏应助PP采纳,获得10
20秒前
香查朵完成签到,获得积分10
21秒前
21秒前
22秒前
23秒前
ljq完成签到,获得积分10
23秒前
23秒前
23秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Molecular Mechanisms of Photosynthesis, 4th Edition 1000
Organic Reactions, Volume 116 1000
Current concepts in cutaneous toxicity : proceedings of the Fourth Conference on Cutaneous Toxicity, Washington, D.C., May 9-11, 1979 1000
The recovery-stress questionnaires : user manual 800
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7259243
求助须知:如何正确求助?哪些是违规求助? 8881303
关于积分的说明 18765467
捐赠科研通 6939565
什么是DOI,文献DOI怎么找? 3201573
关于科研通互助平台的介绍 2375417
邀请新用户注册赠送积分活动 2177348