DocumentCode :
2389501
Title :
Electroactive properties of polyamide/sodium niobate nanowires composites
Author :
David, Ciprian ; Capsal, J. ; Dantras, Eric ; Lacabanne, C.
Author_Institution :
Inst. Carnot CIRIMAT, Univ. de Toulouse, Toulouse, France
fYear :
2011
fDate :
28-31 Aug. 2011
Firstpage :
17
Lastpage :
18
Abstract :
Inorganic sodium niobate nanowires with high crystallinity were synthesized by an hydrothermal process. XRD study of these nanowires revealed a high crystallinity and an orthorhombic crystalline structure. This non centro-symmetric crystalline structure is responsible of the ferroelectric behaviour of these nanowires and by poling the samples above the glass transition of the matrix, the maximum piezoelectric coefficient of the composite was reached within 10 minutes. The magnitude of the poling field (10 kV/mm) is analogous with the one used for NN ceramics; i.e. significantly lower than for piezoelectric polymers (100 kV/mm). The optimum piezoelectricity is 6.5 pC/N for a PA 11/NN nanowires with φ = 0.3. The piezoelectric activity of composite has been compared with PA11/BaTiO3 composites. Piezoelectric activity is higher in PA11/NN nanowires than in PA11/BaTiO3 composites. These lead free composites have a piezoelectric activity close to the one of PZT / polymer composites. These “green composites” could find some applications in flexible, environmentally friendly piezoelectric sensors and actuators.
Keywords :
composite materials; crystal growth from solution; nanowires; piezoelectricity; sodium compounds; NaNbO3; XRD; centro symmetric crystalline structure; electroactive properties; environmentally friendly piezoelectric sensor; glass transition; green composite; hydrothermal process; orthorhombic crystalline structure; piezoelectric coefficient; poling field; polyamide-sodium niobate nanowires composites; Nanowires; Piezoelectric polarization;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Electrets (ISE), 2011 14th International Symposium on
Conference_Location :
Montpellier
ISSN :
2153-3253
Print_ISBN :
978-1-4577-1023-0
Type :
conf
DOI :
10.1109/ISE.2011.6084960
Filename :
6084960
Link To Document :
بازگشت