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Small-scale energy harvesting to power self-powered electronic devices is tremendously increasing. In this context, the ability to combine thermal and mechanical energy harvesting using smart materials deserves more attention for further study. We have presented the feasibility of using P(VDF-TrFE) piezoelectric polymer coupled with NiTi shape memory alloy (SMA) to harvest both mechanical and thermal energy in simple scalable devices. A novel hybrid composite consisting of SMA, and P(VDF-TrFE) has been developed without any complex composites or patterned structures, which couples the piezoelectric effect of the poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) and the shape memory effects of NiTi SMA. We have also fabricated a multi-layer SMA/PEN/P(VDF-TrFE) device using epoxy as an interface and bonding layer. During bending, the P(VDF-TrFE) device with an active area of 3.68 cm2 generated an output voltage of 8 V and an output power of 6.25 µW. When coupled with NiTi SMA to create a hybrid composite thermoelectric material, the device can convert the phase change associated with SMA, and thus thermal energy is converted to mechanical energy and finally into electrical energy. The SMA/P(VDF-TrFE) hybrid composite produced an output voltage of ∼2 V for one cyclic heating and cooling of the device. This is a promising approach for the further development of coupled hybrid energy harvester devices for the powering of small-scale electronic devices such as sensors, MEMS, or biomedical devices. [ABSTRACT FROM AUTHOR]

Second Harmonic Generation (SHG) from BiFeO3 nanocrystals is investigated for the first time to determine their potential as biomarkers for multiphoton imaging. Nanocrystals are produced by an auto-combustion method with 2-amino-2-hydroxymethyl-propane-1,3-diol as a fuel. Stable colloidal suspensions with mean particle diameters in the range 100-120 nm are then obtained after wet-milling and sonication steps. SHG properties are determined using two complementary experimental techniques, Hyper Rayleigh Scattering and nonlinear polarization microscopy. BiFeO3 shows a very high second harmonic efficiency with an averaged hdi coefficient of 79±12 pm/V. From the nonlinear polarization response of individual nanocrystals, relative values of the independent dij coefficients are also determined and compared with recent theoretical and experimental studies. Additionally, the particles show a moderate magnetic response, which is attributed to γ-Fe2O3 impurities. A combination of high nonlinear optical efficiency and magnetic response within the same particle is of great interest for future bio-imaging and diagnostic applications. [ABSTRACT FROM AUTHOR]

ABSTRACT Polymethyl methacrylate (PMMA)/Fe(IO3)3 nanocomposite thin films are obtained by in situ particle generation in microemulsions and subsequent photopolymerization of a mixture containing methyl methacrylate, trimethylolpropane triacrylate, and crystallized iron iodate (Fe(IO3)3) nanorods. Hyper-Rayleigh scattering measurements combined with X-ray diffraction, transmission electron microscopy, and dynamic light scattering are first used to probe in situ the crystallization kinetics of iron iodate nanorods in water-in-oil microemulsions prepared with methyl methacrylate as the oil phase and marlophen NP12 as a surfactant. Trimethylolpropane triacrylate is then added as a crosslinker before spin-coating. Films are deposited on glass substrates for the nonlinear optical characterizations and on silicon wafers for the piezoelectric and mechanical measurements. Nanocomposite films treated by corona discharge are finally characterized through optical microscopy, laser Doppler vibrometry, and Brillouin spectroscopy. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1203-1211, 2013 [ABSTRACT FROM AUTHOR]

Piezoelectric films were prepared by incorporation of lithium niobate (LiNbO3) nanoparticles into copolymer of vinylidene difluoride and trifluoroethylene. Nanoparticles of LiNbO3 with ferroelectric phase were successfully synthesized and dispersed homogenously by ultrasonication in the copolymer matrix without any surfactant or surface functionalization. The nanocomposites were fully characterized by electronic microscopy, X-ray diffraction, differential scanning calorimetry, dynamical mechanical analysis, and piezometer. Surprisingly, the copolymer matrix crystallinity and morphology were not affected by the incorporation of nanoparticles. Therefore the nanocomposites remained good mechanicals properties and high ferroelectricity coupled to nonlinear optical activity thanks to the noncentro symmetric space group of lithium niobate. This could be a novel approach to develop new multifunctional materials. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 [ABSTRACT FROM AUTHOR]

Abstract: New near-infrared luminescent, monoclinic CaAl2O4:Er3+ phosphor was prepared by using the combustion route at furnace temperatures as low as 500°C in a few minutes. Combustion synthesized phosphor has been well characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive analysis of X-ray (EDAX) mapping studies. The luminescence spectra of Er3+-doped calcium aluminate were studied at UV (380nm), vis (488nm) and IR (980nm) excitation. Upon UV and vis excitation, the CaAl2O4:Er3+ phosphor exhibits emission bands at ~523nm and at ~547nm, corresponding to transitions from the 2H11/2 and 4S3/2 erbium levels to the 4I15/2 ground state. A strong luminescence at 1.55μm in the infrared (IR) region due to 4I13/2→4I15/2 transition has been observed in CaAl2O4:Er3+ phosphor upon 980nm CW pumping. In the spectrum of IR-excited up-conversion luminescence, green (~523 and ~547nm) and red (662nm) luminescence bands were present, the latter associated with the 4F9/2→4I15/2 transitions of Er3+ ions. Both excited state absorption and energy transfer may be proposed as processes responsible for the population of the 4S3/2 and 4F9/2 erbium levels upon IR excitation. The mechanisms responsible for the up-conversion luminescence are discussed. [Copyright &y& Elsevier]