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二氧化钛纳米颗粒薄膜的电子性质及其对磷灰石形成能力的影响。

Electronic Properties of TiO2 Nanoparticles Films and the Effect on Apatite-Forming Ability.

作者信息

Löberg Johanna, Perez Holmberg Jenny, Mattisson Ingela, Arvidsson Anna, Ahlberg Elisabet

机构信息

DENTSPLY Implants, Box 14, 431 21 Mölndal, Sweden ; Department of Chemistry and Molecular Biology, University of Gothenburg, 412 96 Gothenburg, Sweden.

出版信息

Int J Dent. 2013;2013:139615. doi: 10.1155/2013/139615. Epub 2013 May 12.

DOI:10.1155/2013/139615
PMID:23737786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3666295/
Abstract

Nanoparticle-covered electrodes have altered properties as compared to conventional electrodes with same chemical composition. The changes originate from the large surface area and enhanced conduction. To test the mineralization capacity of such materials, TiO2 nanoparticles were deposited on titanium and gold substrates. The electrochemical properties were investigated using cyclic voltammetry and impedance spectroscopy while the mineralization was tested by immersion in simulated body fluid. Two types of nucleation and growth behaviours were observed. For smooth nanoparticle surfaces, the initial nucleation is fast with the formation of few small nuclei of hydroxyapatite. With time, an amorphous 2D film develops with a Ca/P ratio close to 1.5. For the rougher surfaces, the nucleation is delayed but once it starts, thick layers are formed. Also the electronic properties of the oxides were shown to be important. Both density of states (DOS) in the bandgap of TiO2 and the active area were determined. The maximum in DOS was found to correlate with the donor density (N d ) and the active surface area. The results clearly show that a rough surface with high conductivity is beneficial for formation of thick apatite layers, while the nanoparticle covered electrodes show early nucleation but limited apatite formation.

摘要

与具有相同化学成分的传统电极相比,覆盖有纳米颗粒的电极具有不同的特性。这些变化源于大的表面积和增强的导电性。为了测试此类材料的矿化能力,将二氧化钛纳米颗粒沉积在钛和金基底上。使用循环伏安法和阻抗谱研究其电化学性质,同时通过浸泡在模拟体液中来测试矿化情况。观察到两种成核和生长行为。对于光滑的纳米颗粒表面,初始成核很快,形成少量羟基磷灰石小核。随着时间的推移,会形成一种钙磷比接近1.5的非晶二维膜。对于较粗糙的表面,成核延迟,但一旦开始,就会形成厚层。氧化物的电子性质也被证明很重要。确定了二氧化钛带隙中的态密度(DOS)和活性面积。发现DOS的最大值与施主密度(Nd)和活性表面积相关。结果清楚地表明,具有高导电性的粗糙表面有利于形成厚的磷灰石层,而覆盖有纳米颗粒的电极显示出早期成核,但磷灰石形成有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/b5104dca10d9/IJD2013-139615.010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/5ce878e2186d/IJD2013-139615.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/cf4456c66c56/IJD2013-139615.002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/336d62a9c56c/IJD2013-139615.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/3b4eb44064dc/IJD2013-139615.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/ac682f073595/IJD2013-139615.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/b5104dca10d9/IJD2013-139615.010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/5ce878e2186d/IJD2013-139615.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/cf4456c66c56/IJD2013-139615.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/32c2bf92811c/IJD2013-139615.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/ce781f73a599/IJD2013-139615.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/4ad116517f41/IJD2013-139615.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/dbf7653b2c81/IJD2013-139615.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/336d62a9c56c/IJD2013-139615.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/3b4eb44064dc/IJD2013-139615.008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/ac682f073595/IJD2013-139615.009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b551/3666295/b5104dca10d9/IJD2013-139615.010.jpg

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