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Xabier Garcia-Casas

Publications and source records attributed to Xabier Garcia-Casas.

9 recordsLinked to original sources

Engineering Chirality in Halide Perovskites

The ability to control chirality in halide perovskites offers new opportunities for circularly polarized photonics, spin-selective electronics, and quantum information technologies. Chirality in halide perovskites is commonly achieved through chiral molecular building blocks or externally imposed photonic architectures. Although both approaches can generate strong chiroptical responses, many spin-dependent functionalities require structural symmetry breaking embedded within the material itself. Here we show that chirality can emerge directly during crystal growth. By combining glancing angle deposition with controlled substrate rotation, we generate highly textured PbI2 nanostructures with growth-controlled crystallographic torsion. X-ray texture analysis reveals that substrate rotation progressively rotates the crystal orientation during growth while preserving the c-axis orientation, resulting in a twisted texture with giant and tuneable chiroptical responses, including ellipticities of 19° and absorption dissymmetry factors approaching 0.6. The chirality programmed during growth is transferred through vapour-phase conversion into multiple halide perovskite compositions, resulting in circularly polarized luminescence with glum values up to 0.23. These findings establish growth-controlled crystallographic torsion as a previously unexplored origin of chirality in halide perovskites.

cond-mat.mtrl-sci↗

Adamantane plasma polymers: fluorine-free vacuum-processable triboelectric thin films for all-triboelectric nanogenerator configurations

Triboelectric nanogenerators (TENGs) are major drivers in on-site power generation for smart devices, enable self-powered sensors, and introduce novel catalytic processes. Here, we present the advantages of adamantane plasma layers as bivalently triboelectric surfaces capable of exhibiting both tribopositive and tribonegative character through simple modification of the synthesis conditions without the need for additives or functionalization. Fabrication facing or backfacing the plasma yields thin film polymers with different dielectric constants, Young's moduli, and secondary electron emission. The conformality, stability, and processability of the polymers enable direct implementation across solid-solid, solid-liquid, and hybrid piezo-triboelectric configurations. Additional texturization by buckling is shown to provide voltage and current outputs as high as 90 V cm2 and 0.6 uA for a 2.8 um (tribonegative) vs. 400 nm (tribopositive) combination. A maximum power density of 2.1 uW cm-2 is generated from salty droplets in a switch-electrode drop-TENG configuration employing a 500 nm-thick tribopositive adamantane polymer as the triboelectric surface. These layers have demonstrated outstanding durability, enabling more than 10^5 cycles in solid-solid nanogenerators and 10^4 droplet impacts in solid-liquid configurations. The synthetic method is environmentally friendly and industrially scalable, making the adamantane plasma polymer a reliable and competitive solution for thin film triboelectric materials.

cond-mat.mtrl-sci↗

Water-resistant hybrid perovskite solar cell -- drop triboelectric energy harvester

Hybrid energy-harvesting systems combining perovskite solar cells (PSCs) with drop-driven triboelectric nanogenerators (D-TENGs) provide continuous power under various weather conditions. However, halide perovskites' vulnerability to moisture hampers widespread use. We present plasma-deposited fluorinated polymers (CFX) as multifunctional encapsulation layers offering water resistance, triboelectric functionality, and > 90 % optical transparency. These conformal, room-temperature, solvent-free coatings protect PSCs without reducing performance; encapsulated cells maintained a PCE of 17.9 %, and devices kept over 50 % of initial PCE after 10 days in high humidity and temperature. CFx layers also enabled compatibility with UV-curable resins, creating a hybrid PSC/D-TENG capable of harvesting solar and rain energy. This device retained 80 % of its performance after 300 hours of humid operation and stayed stable under continuous dripping and illumination for over 5 hours. Optimizing CFx's chemical composition improved triboelectric performance. Using the same CFx layer for encapsulation and triboelectric function, the device achieved 11.6 mA/cm2 short-circuit current under 0.5 sun and 12 V peak voltage per raindrop, enabling simultaneous solar and rain energy harvesting. A self-charging prototype powered LED arrays via a boost converter, demonstrating practical multisource energy harvesting.

cond-mat.mtrl-sci↗

Unlocking the hybrid piezo and pyroelectric nanogenerators performance by SiO2 nanowires confinement in poly(vinylidene fluoride)

We report on the development of a novel flexible piezo/pyro-electric nanogenerator (PPNG) that combines a uniform film of poly(vinylidene fluoride) (PVDF) infiltrated over vertically supported SiO2 nanowires (NWs) to enhance both piezoelectric and pyroelectric energy harvesting capabilities. The synthetic procedure involves a low-temperature multi-step approach, including the soft-template formation of SiO2 NWs on a flexible substrate, followed by the infiltration of a PVDF thin film (TF). The plasma-enabled fabrication of SiO2 NWs facilitated vertical alignment and precise control over the surface microstructure, density, and thickness of the confined nanostructures. These strategic structural systems promote the development of the most favourable electroactive \b{eta}- and γ-phases in the PVDF matrix. Notably, the electrical poling plays a major role in aligning the random dipoles of the PVDF macromolecular chain in a more ordered fashion to nucleate the amplified electroactive phases. As a proof-of-concept, the fabricated PPNG exhibited a significant improvement in the instantaneous piezoelectric output power density (P), ~ 9-fold amplification relative to its bare PVDF TF counterpart. Analogously, the pyroelectric coefficient (p) demonstrated a 4-fold superior performance with referenced PVDF TF based PPNG. Thus, the engineered system of SiO2 NWs@PVDF comprising PPNG offers a promising pathway toward multisource energy harvesting capabilities through efficient energy transduction at mechanical excitation frequencies of 10-12 Hz and across a temperature difference (ΔT) of 9 to 22 K.

cond-mat.mtrl-sci↗

Triboelectric Pixels as building blocks for microscale and large area integration of drop energy harvesters

The ultimate step towards the exploitation of water as a clean and renewable energy source addresses the energies stored in the low frequencies of liquid flows, which demands flexible solutions to adapt to multiple scenarios, from raindrops to waves, including water moving in pipelines and microdevices. Thus, harvesting low-frequency flows is a young concept compared to solar and wind powers, where triboelectric nanogenerators have been revealed as the most promising relevant actors. However, despite widespread attempts by researchers, the drop energy harvesters' output power is still low, mainly because of the limitations in candidates endowed with ideal triboelectric and wetting properties and also the non-optimal and centimetre-scale device architecture that prevents the conversion of the complete kinetic energy of impinging drops. Herein, we disclose a microscale triboelectric nanogenerator that can harvest a high density of electrical power from drops through a single, submillisecond, long-lasting step. The mechanism relies on an instantaneous electrical capacitance variation owing to the high-speed contact of the drops with the electrodes' active area. We discuss the role of the precharged effect of the triboelectric surface in the time characteristic of the conversion event. The capacitive and microscale structure of the device is endowed with a small form factor that allows for the production of densely packed arrays. The proposed architecture can be adjusted to different liquids and scales and is compatible with a variety of triboelectric surfaces, including flexible, transparent, and thin-film approaches.

physics.app-ph↗

Paper-based ZnO self-powered sensors and nanogenerators by plasma technology

Nanogenerators and self-powered nanosensors have shown the potential to power low-consumption electronics and human-machine interfaces, but their practical implementation requires reliable, environmentally friendly and scalable, processes for manufacturing and processing. This article presents a plasma synthesis approach for the fabrication of piezoelectric nanogenerators (PENGs) and self-powered sensors on paper substrates. Polycrystalline ZnO nanocolumnar thin films are deposited by plasma-enhanced chemical vapour deposition on common paper supports using a microwave electron cyclotron resonance reactor working at room temperature yielding high growth rates and low structural and interfacial stresses. Applying Kinetic Monte Carlo simulation, we elucidate the basic shadowing mechanism behind the characteristic microstructure and porosity of the ZnO thin films, relating them to an enhanced piezoelectric response to periodic and random inputs. The piezoelectric devices are assembled by embedding the ZnO films in PMMA and using Au electrodes in two different configurations: laterally and vertically contacted devices. We present the response of the laterally connected devices as a force sensor for low-frequency events with different answers to the applied force depending on the impedance circuit, i.e. load values range, a behaviour that is theoretically analyzed. The vertical devices reach power densities as high as 80 nW/cm2 with a mean power output of 20 nW/cm2. We analyze their actual-scenario performance by activation with a fan and handwriting. Overall, this work demonstrates the advantages of implementing plasma deposition for piezoelectric films to develop robust, flexible, stretchable, and enhanced-performance nanogenerators and self-powered piezoelectric sensors compatible with inexpensive and recyclable supports

physics.app-ph↗

Coarse-grained approach to amorphous and anisotropic materials in Kinetic Monte Carlo thin-films growth simulations: a case study of TiO2 and ZnO by Plasma Enhanced Chemical Vapor Deposition

The growth of amorphous TiO2 and anisotropic-polycrystalline ZnO thin-films is studied by means of coarse-grained three-dimensional kinetic Montecarlo simulations under conditions typically encountered in Plasma Enhanced Chemical Vapor Deposition experiments. The approach developed considers fluctuations in the activation energy for surface diffusion of the coarse particles that are calculated on-the-fly and depends on the mesoscale local morphological/structural landscape. The basis of this approach --which is known to work well to simulate the growth of amorphous materials using a much simpler cubic grid-- has been extended in this work to reproduce not only the morphological characteristics and scaling properties of amorphous TiO2 but also the growth of polycrystalline ZnO with a good approximation, including the evolution of the film texture and textured-grain competition during growth and its dependence on experimental conditions. The results of the simulations have been compared with available experimental data obtained by X-Ray Diffraction, analysis of the texture coefficients, Atomic Force Microscopy and Scanning Electron Microscopy

cond-mat.mtrl-sci↗

Highly anisotropic organometal halide perovskite nanowalls grown by Glancing Angle Deposition

Polarizers are ubiquitous components in optoelectronic devices of daily use as displays, optical sensors or photographic cameras, among others. Yet the control over light polarization is an unresolved challenge as the main drawback of the current display technologies relays in significant optical losses. In such a context, organometal halide perovskites can play a decisive role given their flexible synthesis with under design optical properties . Therefore, along with their outstanding electrical properties have elevated hybrid perovskites as the material of choice in photovoltaics and optoelectronics. Among the different organometal halide perovskite nanostructures, nanowires and nanorods have lately arise as key players for the control of light polarization for lighting or detector applications. Herein, we will present the unprecedented fabrication of highly aligned and anisotropic methylammonium lead iodide (MAPI) perovskite nanowalls by Glancing Angle Deposition of PbI2 under high vacuum followed by CH3NH3I deposition at normal angle. Our approach offers a direct route for the fabrication of perovskite nanostructures virtually on any substrate, including on photovoltaic devices. The unparalleled alignment degree of the perovskite nanowalls provides the samples with strong anisotropic optical properties such as light absorption and photoluminescence, the latter with a maximum polarization ratio of P=0.43. Furthermore, the implementation of the MAPI nanowalls in photovoltaic devices provides them with a polarization-sensitive response, with a maximum photocurrent difference of 2.1 % when illuminating with the near-infrared range of the solar spectrum (>700 nm). Our facile vacuum-based approach embodies a milestone in the development of last generation polarization-sensitive perovskite-based optoelectronic devices such as lighting appliances or self-powered photodetectors.

physics.optics↗

3D core@multishell piezoelectric nanogenerators

The thin film configuration presents obvious practical advantages over the 1D implementation in energy harvesting systems such as easily manufacturing and processing and long lasting and stable devices. However, most of the ZnO-based piezoelectric nanogenerators (PENGs) reported so far relay in the exploitation of single-crystalline ZnO nanowires because their self-orientation in the c-axis and ability to accommodate long deformations resulting in a high piezoelectric performance. Herein, we show an innovative approach aiming to produce PENGs by combining polycrystalline ZnO layers fabricated at room temperature by plasma assisted deposition with supported small-molecule organic nanowires (ONWs) acting as 1D scaffold. The resulting hybrid nanostructure is formed by a single-crystalline organic nanowire conformally surrounded by a three dimensional (3D) ZnO shell that combines the mechanical properties of the organic core with the piezoelectric response of the ZnO layer. In a loop forward towards the integration of multiple functions within a single wire, we have also developed ONW@Au@ZnO nanowires including a gold shell acting as inner nanoscopic electrode. Thus, we have built and compare thin films and 3D core@shell ONW@ZnO and ONW@Au@ZnO PENGs showing output piezo-voltages up to 170 mV. The synergistic combination of functionalities in the ONW@Au@ZnO devices promotes an enhanced performance generating piezo-currents almost twenty times larger than the ONW@ZnO nanowires and superior to the thin film nanogenerators for equivalent and higher thicknesses.

physics.app-ph↗