RESUMO
In this study, poly(2-ethylhexyl acrylate) (PEHA) homopolymer and its copolymer combined with acrylic acid P(EHA-co-AA) were employed as interfaces in two separate Schottky structures. First, both interfaces were grown by initiated chemical vapor deposition (iCVD), which provides much better deposition control and homogeneous coating compared to solution-phase methods. In addition to this advantageous method, the effects of two different polymers, one of which is better able to adhere to the crystal surface on which it is formed than the other, on the optoelectronic properties have been studied. Then, their current-voltage (I-V) and capacitance/conductance-voltage (C/(G/ω)-V) characteristics were investigated both in the dark and under illumination. The basic electrical parameters and the illumination-induced profile of the surface state (Nss) were probed by I-V and C-V measurements for two samples. A decrease in the barrier height (BH) and, consequently, a significant increase in the photocurrent were observed under illumination. Striking changes in series resistance (Rs) values are also highlighted. The photocapacitance and conductance characteristics indicated that the structures could be considered not only as photodiodes but also as photocapacitors. Moreover, the voltage-dependent changes of some photodetector parameters, such as responsivity (R), sensitivity (S), and specific detectivity (D*), along with the transient photocurrent characteristics, are discussed for both structures. Therefore, we can say that the strong changes in these parameters, which figure the merit of photodiode and photodetector applications, depending on the voltage and under illumination, prove that it is a study carried out in accordance with the purpose and so they can be used in electronic and optoelectronic applications.
RESUMO
RATIONALE: Butane is an important industrial chemical in which photo-processes are very important for the initiation of reactions. Recent advances in nanosecond pulsed laser technology have led to high laser intensities being available to researchers to enable these photo-processes to be studied in compounds such as butane. METHODS: The photo-decomposition, dissociation and combustion mechanisms in the neutral butane molecule have been studied in detail, by investigating the multiphoton (MP) dissociative ionisation of its n- and i-isomers, using a time-of-flight mass spectrometer connected to a high power nanosecond laser system. The laser used was a Nd:Yag with a 5 ns pulse width operated at the fundamental wavelength (1064 nm) and the doubled and tripled wavelengths (532 nm and 355 nm). The fragmentation patterns for the isomers were determined for the three wavelengths as a function of laser intensity. Similar laser intensities of between 10(10) and 10(13) W/cm(2) were used at the three wavelengths: 1064, 532 and 355 nm. RESULTS: The mass spectra of each isomer of the butane molecule display a very weak molecular ion and are dominated by fragment ion peaks. The degree of fragmentation increases as the laser intensity increases. CONCLUSIONS: Depending on the wavelength some significant differences in the mass spectra of the two isomers were detected and it has been concluded that the isomerisation of i-butane to n-butane is a process which is faster than the duration of the laser pulse used.
