强化锐钛矿/金红石混合相TiO2 @ SiO2纳米颗粒的电化学性能和光催化活性

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
S. Nirmala, M. Jose
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引用次数: 0

摘要

这项工作提供了一个全面的研究锐钛矿/金红石混合相TiO2@SiO2核壳纳米颗粒的电化学和光催化活性。通过x射线衍射分析,确定了不同焙烧温度下锐钛矿和金红石相的调谐质量百分比。利用红外光谱和拉曼光谱研究了双相的不同化学键和活性能模式。从紫外可见光谱中观察到,混合相组成物的吸光度强度逐渐红移。通过透射电镜分析证实了其球形形貌、较小的粒径和核壳结构。XPS分析检测到Ti4+、Si4+元素普遍存在。TiO2@SiO2核壳纳米颗粒的最高BET表面积测量值(522 m2/g)增强了光活性,降解刚果红染料的效率达到95%。此外,混合相TiO2@SiO2纳米颗粒在电流密度为1 a /g-1的情况下,具有显著的471.8 F/g-1的比电容,循环次数为5000次,电容保持率为94%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced electrochemical performance and photocatalytic activity of mixed-phase anatase/rutile TiO2 @ SiO2 core-shell nanoparticles
This work provides a comprehensive investigation of the electrochemical and photocatalytic activity of anatase/rutile mixed-phase TiO2@SiO2 core-shell nanoparticles. From X-ray diffraction analysis, the tuned weight percentage of the anatase and rutile phases for varying calcination temperatures was determined. The different chemical bonds and active energy modes of the dual phase were studied using the FTIR and Raman analysis. The mixed-phase compositions exhibited a gradual redshift in absorbance strength as observed from the UV-Visible spectroscopy. The spherical morphology, lower particle size, and the core-shell formation were confirmed using TEM analysis. The XPS analysis detected the prevalent presence of Ti4+, Si4+ elements. The highest BET surface area measurements (522 m2/g) of TiO2@SiO2 core-shell nanoparticles enhanced the photoactivity to achieve 95% efficiency in degrading Congo red dye. Also, the mixed-phase TiO2@SiO2 nanoparticles have shown a remarkable specific capacitance of 471.8 F/g-1 at the current density of 1 A/g-1 for 5000 cycles with 94% capacitance retention.
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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