arXiv subjects

Xabier Rodríguez-Martínez

Publications and source records attributed to Xabier Rodríguez-Martínez.

4 recordsLinked to original sources

arXiv2026

Exploring the Potential of Ternary Blending for Two and Three-Junction RAINBOW Solar Cells

The efficiency of organic photovoltaics (OPV) has been steadily increasing over the past decade until reaching the 20\% milestone. Multijunction architectures provide a promising approach to further enhance performance. Here we explore the potential of a spectral splitting geometry, referred to as RAINBOW, in which subcells are placed side-by-side and externally connected, thus minimizing the fabrication and current matching challenges found in vertically stacked configurations. First, we tested 7 different binaries with bandgaps spanning from 1.98 to 1.16 eV. The systems with the widest and narrowest gaps suffered greater losses and so we evaluate if ternary mixing could help to overcome these limitations by evaluating 5 different ternaries. Generally speaking, ternary mixing tunes the Voc, and when morphology and energy levels are well aligned, the overall PCE can be boosted in the spectral region where the subcell should absorb, as is the case for PTB7-Th:COTIC-4F:BTP-eC9 when operating as red subcell. Device simulations help to identify the 2-junction and 3-junction configurations with highest PCEs, all of which include ternaries. We fabricate proof-of-concept RAINBOW devices using scalable methods in which the subcells are deposited by meniscus-guided blade coating. The efficiency improves from 12.9\% in single-junction devices to 15.9\% in 2-junction devices (16.4\% in simulations) and 17.3\% in 3-junction devices (17.7\% in simulations), confirming the viability of the RAINBOW architecture for scalable, high-efficiency OPVs. Finally, detailed balance analysis indicates that the potential of this geometry can be very high provided that high efficiency wide bandgap (2-2.5 eV) materials become available.

cond-mat.mtrl-sci↗

arXiv2025

Ion-Exchange Doping of Semiconducting Single-Walled Carbon Nanotubes

Semiconducting single-walled carbon nanotubes (SWCNTs) are a promising thermoelectric material with high power factors after chemical p- or n-doping. Understanding the impact of dopant counterions on charge transport and thermoelectric properties of nanotube networks is essential to further optimize doping methods and to develop better dopants. Here, we utilize ion-exchange doping to systematically vary the size of counterions in thin films of small and large diameter, polymer-sorted semiconducting SWCNTs with AuCl3 as the initial p-dopant and investigate the impact of ion size on conductivity, Seebeck coefficients and power factors. Larger anions are found to correlate with higher electrical conductivities and improved doping stability, while no significant effect on the power factors is found. Importantly, the effect of counterion size on the thermoelectric properties of dense SWCNT networks is not obscured by morphological changes upon doping. The observed trends of carrier mobilities and Seebeck coefficients can be explained by a random resistor model for the nanotube network that accounts for overlapping Coulomb potentials leading to the formation of an impurity band whose depth depends on the carrier density and counterion size. These insights can be applied more broadly to understand the thermoelectric properties of doped percolating disordered systems, including semiconducting polymers.

cond-mat.mtrl-sci↗

arXiv2025

Bandgap-Dependent Doping of Semiconducting Carbon Nanotube Networks by Proton-Coupled Electron Transfer for Stable Thermoelectrics

Networks of semiconducting single-walled carbon nanotubes (SWNTs) are a promising material for thermoelectric energy harvesting due to their mechanical flexibility, solution processability, high Seebeck coefficients and high electrical conductivities after chemical p- or n-doping. Here, we demonstrate that proton-coupled electron transfer (PCET) with benzoquinone (BQ) as the oxidant and lithium bis(trifluoromethylsulfonyl)imide (Li[TFSI]) for electrolyte counterions is a promising method for p-doping of polymer-sorted semiconducting SWNT networks. The achieved doping levels, as determined from absorption bleaching, depend directly on both the pH of the aqueous doping solutions and the bandgap (i.e., diameter) of the nanotubes within the network. Fast screening of different nanotube networks under various doping conditions was enabled by a high-throughput setup for thermoelectric measurements of five samples in parallel. For small-bandgap SWNTs, PCET-doping is sufficient to reach the maximum thermoelectric power factors, which are equal to those obtained by conventional methods. In contrast to other doping methods, the electrical conductivity of PCET-doped SWNTs remains stable over at least 5 days in air. These results confirm PCET to be a suitable approach for more environmentally friendly and stable doping of semiconducting SWNTs as promising thermoelectric materials.

physics.app-ph↗

arXiv2016

Dynamic disorder, phonon lifetimes, and the assignment of modes to the vibrational spectra of methylammonium lead halide perovskites

We present Raman and terahertz absorbance spectra of methylammonium lead halide single crystals (MAPbX3, X = I, Br, Cl) at temperatures between 80 and 370 K. These results show good agreement with density-functional-theory phonon calculations.1 Comparison of experimental spectra and calculated vibrational modes enables confident assignment of most of the vibrational features between 50 and 3500 cm-1. Reorientation of the methylammonium cations, unlocked in their cavities at the orthorhombic-to-tetragonal phase transition, plays a key role in shaping the vibrational spectra of the different compounds. Calculations show that these dynamics effects split Raman peaks and create more structure than predicted from the independent harmonic modes. This explains the presence of extra peaks in the experimental spectra that have been a source of confusion in earlier studies. We discuss singular features, in particular the torsional vibration of the C-N axis, which is the only molecular mode that is strongly influenced by the size of the lattice. From analysis of the spectral linewidths, we find that MAPbI3 shows exceptionally short phonon lifetimes, which can be linked to low lattice thermal conductivity. We show that optical rather than acoustic phonon scattering is likely to prevail at room temperature in these materials.

cond-mat.mtrl-sci↗