Jean-Luc Garden

Stability of pentacene top gated thin film transistors

We report on the stability of top gated pentacene field effect transistors processed on Kapton™ with Parylene-C as gate dielectric. The influence of bias stress and ambient atmosphere on device characteristics were investigated. Combined influence of moisture and gate bias stress led to an increase of depletion current and subthreshold slope as well as a drift of onset voltage and threshold voltage. We show that devices stressed in the off state exhibit a high stability.

Thermal denaturation of DNA studied with neutron scattering.

The melting transition of DNA, whereby the strands of the double-helix structure completely separate at a certain temperature, has been characterized using neutron scattering. A Bragg peak from B-form fiber DNA has been measured as a function of temperature, and its widths and integrated intensities have been interpreted using the Peyrard-Bishop-Dauxois model with only one free parameter. The experiment is unique, as it gives spatial correlation along the molecule through the melting transition where other techniques cannot.

Physical kinetics and thermodynamics of phase transitions probed by dynamic nanocalorimetry

A specific ac nanocalorimeter is presented for the study of kinetics in phase transitions. This apparatus designed by means of microfabrication technologies requires a 50‐μm-thick solid or liquid sample. The use of the ac calorimetric method allows an operating frequency range around two decades combined with a very high sensitivity. The ability of this apparatus for thermal spectroscopy is illustrated by measuring the thermal behavior of a homopolymer, the polytetrafluoroethylene, which exhibits two phase transitions at room temperature. The variation of the thermal frequency allows the observation of kinetic effects directly seen on the thermodynamic properties (enthalpy and heat capacity). We demonstrate the possibility of extracting a quantitative value of the kinetic time constant occurring at a first-order phase transition and consequently the capabilities offered by highly sensitive ac calorimetry to investigate direct thermal dynamics in macromolecular samples.

Highly sensitive parylene membrane-based ac-calorimeter for small mass magnetic samples

We report the microfabrication and operation of a highly sensitive ac-calorimeter designed to characterize small mass magnetic systems operating at very low frequencies (from 0.1 to 5 Hz) in a temperature range from 20 to 300 K. The calorimetric cell is built in the center of a 500 nm thick polymeric membrane of parylene C held up by a Cu frame. On both sides of the membrane defining a three layer structure, electrical leads, heater, and thermometer are deposited as thin film layers of NbN(x), with different nitrogen contents, taking benefit of the poor thermal conductance of niobium nitride to thermally isolate the system. This suspended structure ensures very low heat capacity addenda with values in the microJ/K over the 1 mm(2) area of the measurement cell. The structuring of the membrane along with suspending of the sensing part only by the parylene bridges leads to a highly reduced thermal link. The calorimeter has been characterized as a function of frequency, temperature, and magnetic field. The thermal link measured is really small reaching values well below 10(-8) W/K at 50 K. With these characteristics the frequency of adiabaticity is typically around few hertz and energy exchanges as small as 1 pJ can be detected. Measurements have been performed on Co/Au thin films and on the GdAl(2) microcrystal where the ferromagnetic phase transition is clearly evidenced.

Affinity and its derivatives in the glass transition process

The thermodynamic treatment of the glass transition remains an issue of intense debate. When associated with the formalism of non-equilibrium thermodynamics, the lattice-hole theory of liquids can provide new insight in this direction, as has been shown by Schmelzer and Gutzow [J. Chem. Phys. 125, 184511 (2006)], by Möller et al. [J. Chem. Phys. 125, 094505 (2006)], and more recently by Tropin et al. [J. Non-Cryst. Solids 357, 1291 (2011); ibid. 357, 1303 (2011)]. Here, we employ a similar approach. We include pressure as an additional variable, in order to account for the freezing-in of structural degrees of freedom upon pressure increase. Second, we demonstrate that important terms concerning first order derivatives of the affinity-driving-force with respect to temperature and pressure have been previously neglected. We show that these are of crucial importance in the approach. Macroscopic non-equilibrium thermodynamics is used to enlighten these contributions in the derivation of C(p),κ(T), and α(p). The coefficients are calculated as a function of pressure and temperature following different theoretical protocols, revealing classical aspects of vitrification and structural recovery processes. Finally, we demonstrate that a simple minimalist model such as the lattice-hole theory of liquids, when being associated with rigorous use of macroscopic non-equilibrium thermodynamics, is able to account for the primary features of the glass transition phenomenology. Notwithstanding its simplicity and its limits, this approach can be used as a very pedagogical tool to provide a physical understanding on the underlying thermodynamics which governs the glass transition process.

Depth-dependence of electrical conductivity of diamondlike carbon films

The electrical behavior of diamondlike carbon (DLC) has been measured as a function of depth. The amorphous carbon (a-C) films are deposited by pulsed laser deposition using two complementary setups: a femtosecond (fs) and a nanosecond (ns) pulse lasers. It is demonstrated through four probe resistance measurements and contact resistance mapping that the fs DLC are electrically heterogeneous in thickness. The presence of a thick sp2 rich layer on top is evidenced for fs a-C and is apparently away in the sp3 rich ns a-C. It is attributed to different subplantation processes between ns and fs a-C films.

Purification of A-Form DNA Fiber Samples by the Removal of B-Form DNA Residues

To date, fiber diffraction on A-form NaDNA has always shown a B-form contamination. Here we have used optic microscopy, calorimetry, and neutron scattering techniques to define a method to obtain DNA fibres samples whose molecules are purely in the A-form. When the impure sample is heated to 320 K, the DNA molecules in the B-form undergo a transition into the A-form. Our studies have modified the accepted phase diagram for NaDNA films by including the dependence of temperature crucial for the purification of A-form samples by removal of B-form contamination.

Glassy behavior of denatured DNA films studied by differential scanning calorimetry.

We use differential scanning calorimetry (DSC) to study the properties of DNA films, made of oriented fibers, heated above the thermal denaturation temperature of the double helical form. The films show glassy properties that we investigate in two series of experiments, a slow cooling at different rates followed by a DSC scan upon heating and aging at a temperature below the glass transition. Introducing the fictive temperature to characterize the glass allows us to derive quantitative information on the relaxations of the DNA films, in particular to evaluate their enthalpy barrier. A comparison with similar aging studies on PVAc highlights some specificities of the DNA samples.

Boson peak, heterogeneity and intermediate-range order in binary SiO 2 -Al 2 O 3 glasses

In binary aluminosilicate liquids and glasses, heterogeneity on intermediate length scale is a crucial factor for optical fiber performance, determining the lower limit of optical attenuation and Rayleigh scattering, but also clustering and precipitation of optically active dopants, for example, in the fabrication of high-power laser gain media. Here, we consider the low-frequency vibrational modes of such materials for assessing structural heterogeneity on molecular scale. We determine the vibrational density of states VDoS g(ω) using low-temperature heat capacity data. From correlation with low-frequency Raman spectroscopy, we obtain the Raman coupling coefficient. Both experiments allow for the extraction of the average dynamic correlation length as a function of alumina content. We find that this value decreases from about 3.9 nm to 3.3 nm when mildly increasing the alumina content from zero (vitreous silica) to 7 mol%. At the same time, the average inter-particle distance increases slightly due to the presence of oxygen tricluster species. In accordance with Loewensteinian dynamics, this proves that mild alumina doping increases structural homogeneity on molecular scale.

Highly sensitive pseudo-differential ac-nanocalorimeter for the study of the glass transition

We present a nanocalorimeter designed for the measurement of the dynamic heat capacity of thin films. The microfabricated sensor, the thermal conditioning of the sensor, as well as the highly stable and low noise electronic chain allow measurements of the real and imaginary parts of the complex specific heat with a resolution Δ C/C of about 10(-5). The performances of this quasi-differential nanocalorimeter were tested on a model of polymeric glass-former, the polyvinyl acetate (PVAc). The high stability and low noise of the device are essential for accurate studies on non-equilibrium slow relaxing systems such as glasses.