个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:大阪府立大学
学位:博士
所在单位:物理学院
学科:光学. 凝聚态物理. 微电子学与固体电子学
办公地点:物理学院333室
电子邮箱:lpan@dlut.edu.cn
Ag@C Core-Shell Colloidal Nanoparticles Prepared by the Hydrothermal Route and the Low Temperature Heating-Stirring Method and Their Application in Surface Enhanced Raman Scattering
点击次数:
论文类型:期刊论文
发表时间:2012-06-07
发表刊物:JOURNAL OF PHYSICAL CHEMISTRY C
收录刊物:SCIE、EI、Scopus
卷号:116
期号:22
页面范围:12283-12294
ISSN号:1932-7447
摘要:Silver nanoparticles (AgNPs) with diameters in the range 40-80 nm have been synthesized by the hydrothermal route and the low temperature heating-stirring method. The influences of reaction time, reactant concentration, and temperature on the AgNP growth have been systemically studied. Experimental surface enhanced Raman scattering (SERS) results show that AgNPs prepared under different temperature and time exhibit a large difference in enhanced SERS signals for rhodamine 6G (10(-6) M). Ag@C core-shell NPs have been proved to be formed by using the above two methods, and the carbon shell thickness is gradually increased with increasing reaction time and temperature. It is found that Ag@C NPs with a thick shell (more than 3 nm) have a very low SERS activity, while those with an ultrathin film (less than 1 nm) have a high SEAS activity, indicating that carbon shell thickness is a key factor affecting the SERS, which has also been evaluated by finite-difference time-domain simulation. The existence of an ultrathin carbon shell around the AgNP can decrease its surface electric property; then Ag@C NP aggregates are easily formed which may produce the higher hot spots than the bare AgNPs. In addition, this kind of Ag@C NPs exhibits a long SERS-active shelf life (6 months), because the carbon shell can protect AgNPs from oxidation.