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The processability and optoelectronic properties of organic semiconductors can be tuned and manipulated via chemical design. The substitution of the alkyl side chains by oligoethers has recently been successful for applications such as bioelectronic sensors and photocatalytic water-splitting. The carbon-oxygen bond in oligoethers is likely to render the system softer and more prone to dynamical disorder that can be detrimental to charge transport for example. We use neutron spectroscopy, X-Ray diffraction (XRD), differential scanning calorimetry (DSC) and polarized optical microscopy to study the effect of the substitution of n-hexyl (Hex) by triethylene glycol (TEG) on the structural dynamics of two organic semiconductors: a phenylene-bithiophene-phenylene (PTTP) molecule and a fluorene-co-dibenzothiophene (FS) polymer. Counterintuitively, inelastic neutron scattering (INS) reveals a softening of the modes of PTTP and FS with Hex side chains, pointing towards an increased dynamical disorder in these systems. However, T-dependent X-Ray and neutron diffraction, INS and DSC evidence an extra reversible transition close to room temperature (RT) for PTTP with TEG side chains. The observed transition, not accompanied by a change in birefringence, can also be observed by quasi-elastic neutron scattering. A fastening of the TEG side chains dynamics is observed in the case of PTTP and not FS. We therefore assign this transition to the melt of the TEG side chains which are promoting dynamical order at RT, but if crystallising, may introduce an extra reversible structural transition above RT leading to thermal instabilities. A deeper understanding of side chain polarity and structural dynamics can help guide materials design and navigate the intricate balance between electronic charge transport and aqueous swelling, sought for a number of emerging organic electronic and bioelectronic applications.
We develop two new amphiphilic molecules that are shown to act as efficient surfactants for carbon nanotubes in non-polar organic solvents. The active conjugated groups, which are highly attracted to graphene nanotube surface, are based on pyrene and
Amorphous organic semiconductors based on small molecules and polymers are used in many applications, most prominently organic light emitting diodes (OLEDs) and organic solar cells. Impurities and charge traps are omnipresent in most currently availa
We generalize the Wannier interpolation of the electron-phonon matrix elements to the case of polar-optical coupling in polar semiconductors. We verify our methodological developments against experiments, by calculating the widths of the electronic b
We combine infrared spectroscopy, nano-indentation measurements, and emph{ab initio} simulations to study the evolution of structural, elastic, thermal, and electronic responses of the metal organic framework MOF-74-Zn when loaded with H$_2$, CO$_2$,
LiOsO$_3$ undergoes a continuous transition from a centrosymmetric $Rbar{3}c$ structure to a polar $R3c$ structure at $T_s=140$~K. By combining transport measurements and first-principles calculations, we find that $T_s$ is enhanced by applied pressu