arXiv subjects

Jaime Martin

Publications and source records attributed to Jaime Martin.

5 recordsLinked to original sources

arXiv2021

Rationalizing the influence of tunable energy levels on quantum efficiency to design optimal non-fullerene acceptor-based ternary organic solar cells

Non-fullerene acceptor (NFA)-based ternary bulk heterojunction solar cells (TSC) are the most efficient organic solar cells (OSCs) today due to their broader absorption and quantum efficiencies (QE) often surpassing those of corresponding binary blends. We study how the energetics driving charge transfer at the electron donor:electron acceptor (D/A) interfaces impact the QE in blends of PBDB-T-2F donor with several pairs of lower bandgap NFAs. As in binary blends, the ionization energy offset between donor and acceptor ({\Delta}IE) controls the QE and maximizes for {\Delta}IE > 0.5 eV. However, {\Delta}IE is not controlled by the individual NFAs IEs but by their average, weighted for their blending ratio. Using this property, we improved the QE of a PBDB-T-2F:IEICO binary blend that had an insufficient {\Delta}IE for charge generation by adding a deep IE third component: IT-4F. Combining two NFAs enables to optimize the D/A energy alignment and cells' QE without molecular engineering.

physics.app-ph↗

arXiv2021

Formation of a highly ordered red phase in a MEH-PPV: polystyrene pseudogels

In this work, we demonstrate the formation of a "red-phase" poly[2-methoxy, 5-(2'- ethyl-hexoxy)-1,4-phenylene vinylene-PPV] (MEH-PPV) embedded into a host matrix of highly entangled ultra-high molecular weight polystyrene (MEH-PPV/UHMW PS pseudogel) that allows the simple processing of the MEH-PPV solutions. We processed a "red-phase" in the gel, the gel shows that the features what have beed demonstrated in the solution can be observed in the processable gel for optoelectronics applications. [Yamagata, Hajime, and Hestand, Nicholas J. and Spano, Frank C. and Kohler, Anna and Scharsich, Christina and Hoffmann, Sebastian T. and Bassler, Heinz, The Journal of Chemical Physics, 2013, 139, 114903]

cond-mat.mtrl-sci↗

arXiv2021

Common high-performance semiconducting polymers are not amorphous but semi-para-crystalline

Precise determination of the solid-state microstructure of semiconducting polymers is of paramount importance for the further development of these materials in various organic electronic technologies. Yet, prior characterization of the ordering of semiconducting polymers often resulted in conundrums in which X-ray scattering and microscopy yielded seemingly contradicting results. Here, based on fast scanning calorimetry, we introduce for the first time the concept of the semi-para-crystallinity and measurement of the degree of para-crystallinity (ordered volume/mass fraction) in a set of materials that previously eluded understanding. In combination with lattice distortion determination within para-crystals (g-parameter from X-ray scattering) and nanomorphology, the complete solid-state microstructure is correlated with device properties. Our data show that the long-range charge carrier transport in these materials is more sensitive to the interconnection of para-crystal units than to the amount of structural order itself.

cond-mat.mtrl-sci↗

arXiv2019

Microstructural control suppresses thermal activation of electron transport at room temperature in polymer transistors

Recent demonstrations of inverted thermal activation of charge mobility in polymer field-effect transistors have excited the interest in transport regimes not limited by thermal barriers. However, rationalization of the limiting factors to access such regimes is still lacking. An improved understanding in this area is critical for development of new materials, establishing processing guidelines, and broadening of the range of applications. Here we show that precise processing of a diketopyrrolopyrrole-tetrafluorobenzene-based electron transporting copolymer results in single crystal-like and voltage-independent mobility with vanishing activation energy above 280 K. Key factors are uniaxial molecular alignment and thermal annealing at temperatures within the melting endotherm of films. Experimental and computational evidence converge toward a picture of electrons being delocalized within crystalline domains of increased size. Residual energy barriers introduced by disordered regions are bypassed in the direction of molecular alignment by a more efficient interconnection of the ordered domains following the annealing process.

cond-mat.mtrl-sci↗

arXiv2017

A review on the progress of polymer nanostructures with modulated morphologies and properties, using nonporous AAO templates

Polymers with the same chemical composition can provide different properties by reducing the dimension or simply by altering their nanostructure. Recent literature works report hundreds of examples of advances methods in the fabrication of polymer nanostructures accomplished following different approaches, soft lithography, self-assembly routes, template assisted methods, etc. Polymer nanostructures with modulated morphologies and properties can be easily achieved from anodized aluminum oxide (AAO) templates assisted methods. In the last decade, fabrication of polymer nanostructures in the nanocavities of AAO has raised a great interest since allows the control and tailoring of dimension of a huge number of polymer and polymer-based composites materials. The fact that polymer dimension can be adjusted allow the study of size-dependency properties. Moreover, modulated polymer nanostructures can be designed for specific applications from AAO templates methods. Taking into account the last considerations, this review present an overview of recent and new insights in the fabrication methods of polymer nanostructures from hard porous Anodic Aluminum Oxide (AAO) templates with emphasis on the study of polymer structure/property relationship at nanometric scale and stressing the potential interest in particular applications.

cond-mat.mtrl-sci↗