Polymer-BaTiO3 composites: Dielectric constant and vapor sensing properties in chemocapacitor applications

被引:12
作者
Manoli, Kyriaki [1 ,2 ]
Oikonomou, Petros [2 ]
Valamontes, Evangelos [3 ]
Raptis, Ioannis [2 ]
Sanopoulou, Merope [1 ]
机构
[1] Natl Ctr Sci Res Demokritos, Inst Phys Chem, Aghia Paraskevi 15310, Greece
[2] Natl Ctr Sci Res Demokritos, Inst Microelect, Aghia Paraskevi 15310, Greece
[3] Technol Educ Inst Athens, Dept Elect Engn, Egaleo, Greece
关键词
nanocomposites; dielectric properties; sensors; barium titanate; capacitive sensors; ORGANIC VAPORS; THIN-FILMS; HUMIDITY; SENSORS; NANOCOMPOSITES; FABRICATION; CAPACITORS; CERAMICS; SYSTEM;
D O I
10.1002/app.35362
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this work, composite materials, prepared by inclusion of various amounts of BaTiO3 nanoparticles in PBMA and PHEMA polymer matrices, were characterized in respect to their dielectric properties and then used as the sensing layer of capacitive-type sensors. BaTiO3 was found to be less effective in enhancing the permittivity of PHEMA, as compared to PBMA, in the range of 1 kHz1 MHz, possibly due to the observed lower quality of dispersion in the polymer matrix and the higher polarity of the polymer in the former case. The response of the composite-based chemocapacitors to four vapor analytes, covering a wide range of dielectric constants, was studied in relation to the BaTiO3 load. In all cases, with increasing amount of BaTiO3 load, the absolute value of capacitance response was increased, due to the corresponding increase of the initial capacitance of the sensing composite layer. However, the corresponding normalized (to the initial capacitance of the sensing composite layer) capacitance values were reduced, due to the decreased volume fraction of the sorbing polymer material in the composite matrix. An exception to this trend, observed upon exposure of the PBMA/BaTiO3 chemocapacitors to low humidity levels, is also presented and discussed. (C) 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
引用
收藏
页码:2577 / 2584
页数:8
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