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Ana Borras

Publications and source records attributed to Ana Borras.

At least 19 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{\deg} 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

Tunable Conformal Graphene Growth on Oxide Nanotube scaffolds: Towards Superwettable Hierarchical 2D-3D Architectures

Hierarchical hybrid nanoarchitectures that integrate vertically oriented graphene nanowalls, GNWs, with metal oxide, MeOx, nanotube scaffolds offer versatile platform for smart surfaces, nanoelectronics, and electrochemical technologies. Herein we present rapid, dry, plasma-assisted fabrication route that enables direct and conformal growth of GNWs on mechanically robust MeOx nanoforests. The method combines supported single-crystalline organic nanowires as a 1D soft template with sequential plasma-enabled oxide deposition and GNW growth, all performed under mild temperature, power, and vacuum conditions. This approach yields an unprecedented 2D-3D hierarchical architecture consisting of tunable-thickness MeOx nanotubes uniformly decorated with radially oriented graphene nanosheets, forming re-entrant, multiscale surface. Resulting hierarchical roughness imparts fluorine-free, long-term omniphobicity, with contact angles exceeding 170 degree for water, bovine serum, and other complex fluids. GNWs dominate the wetting response across TiO2, Al2O3, and SiO2 nanotube scaffolds, effectively decoupling surface behavior from intrinsic oxide chemistry and maintaining robust repellency under UV irradiation and water condensation. Comprehensive SEM, TEM, XPS, angle-resolved NEXAFS, and Raman analyses elucidate growth mechanism and confirm preservation of the sp2 graphitic framework, together with controlled degree of edge functionalization. Overall, this work establishes universal, substrate-compatible, low-temperature, and scalable route for the fabrication of tunable graphene-metal oxide nano-microstructured multifunctional surfaces.

cond-mat.mtrl-sci

Polycrystalline ferroelectric croconic acid for multisource environmental energy harvesting

The development of organic ferroelectric materials through scalable and simplified fabrication routes remains a major challenge for next-generation energy-harvesting technologies. Here, polycrystalline croconic acid (CA) thin films are fabricated by vacuum sublimation onto Ar plasma-treated flexible substrates and stabilized by in situ encapsulation with an adamantane-based remote plasma polymer. This solvent-free strategy effectively suppresses surface degradation under ambient conditions, providing long-term stability. Piezoresponse force microscopy confirms robust ferroelectricity with an oblique polarization orientation, well-defined domains, and low nanoscale coercive fields. The films were integrated into multilayer piezoelectric and pyroelectric devices. The piezoelectric performance strongly depends on film thickness, while embedding the CA layer between dielectric polymeric films significantly improves the macroscopic response, reaching power densities of up to 37 microW m-2 for ca. 2 micrometer CA films. Despite the common assumption that high crystallinity is required to sustain ferro-, piezo-, and pyroelectricity, these polycrystalline CA films exhibit remarkable RT pyroelectricity, a property not previously demonstrated in CA-based devices. A pyroelectric coefficient of ca. 10 microC m-2 K-1 highlights a functional response comparable to that of well-established organic and inorganic pyroelectric materials, demonstrating the potential of CA thin films for thermal energy harvesting. Beyond their functional performance, the proposed low-T fabrication route combines deposition and encapsulation in a single in situ process, simplifying device fabrication. Its compatibility with scalable vacuum technologies, flexible substrates, and further process optimization makes this approach highly promising for developing low-cost, lead-free, multisource energy-harvesting systems.

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

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 {\gamma}-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 ({\Delta}T) of 9 to 22 K.

cond-mat.mtrl-sci

Enhanced Luminous Transmission and Solar Modulation in Thermochromic VO2 Aerogel-Like Films via Remote Plasma Deposition

Vanadium dioxide (VO2) is a thermochromic material that undergoes a phase transition from a monoclinic semiconducting state to a rutile metallic state at 68 degrees C, a temperature close to room temperature. This property makes VO2 particularly valuable in applications such as optical and electrical switches, data storage, neuromorphic computing, and remarkably dynamic smart windows for solar radiation control. VO2 typically needs to be synthesized for these applications as nanostructured thin films. Over the past few decades, significant efforts have been made to control the thermochromic properties of VO2 through crystal structure tuning, doping, and the development of VO2 nanocomposites. Additionally, introducing nano- and mesoporosity has been shown to enhance the optical properties of thermochromic VO2 films. This study presents a methodology for producing highly porous, aerogel-like V2O5 films, which can be thermally processed to form aerogel-like VO2 films. This process is based on sequential plasma polymerization and plasma etching to produce aerogel-like V2O5 films that are annealed to yield ultraporous nanocrystalline VO2 films. The sacrificial vanadium-containing plasma polymers are obtained by remote plasma-assisted vacuum deposition (RPAVD) using vanadyl porphyrin as a precursor and Ar as plasma gas. The aerogel-like VO2 films show exceptional thermochromic performance with luminous transmittances higher than 54%, solar modulation up to 18.8%, and IR modulation up to 35.5%. The presented plasma methodology is versatile, allowing both the synthesis of VO2 plasmonic structures to enhance the thermochromic response and the encapsulation of films to improve their stability in air dramatically. Additionally, this solvent-free synthetic method is fully compatible with doping procedures, scalable, and holds great potential for designing and optimizing smart window coatings.

physics.app-ph

Low-Temperature Remote Plasma Synthesis of Highly Porous TiO$_2$ as Electron Transport Layers in Perovskite Solar Cells

Halide perovskite solar cells (PSCs) offer high efficiency and low costs, making them key for future photovoltaics. Optimizing charge transport layers is crucial, with porous TiO$_2$ widely used as electron transport layers (ETL) due to its energy alignment, transparency, and abundance. However, its efficiency relies on crystallinity requiring high-temperature processing (>450$^\circ$C), increasing costs and limiting flexible substrates. Low-temperature wet-chemical methods face scalability issues due to material waste and hazardous solvents. In this context, plasma-based technologies are emerging as a more efficient and sustainable alternative to oxide-based ETLs. This study presents the synthesis of TiO$_2$ layers using an advanced plasma method combining remote plasma-assisted vacuum deposition (RPAVD) and soft plasma etching (SPE) at mild temperatures (<200$^\circ$C), allowing control of microstructure and porosity. The resulting nanocolumnar film, decorated with a highly porous aerogel-like layer, enhances optical and electronic properties. These plasma-synthesized TiO$_2$ layers are antireflective and improve the efficiency in porous n-i-p PSCs, matching the performance of high-temperature reference cells. These PSCs achieve a champion PCE of 14.6%, a high value compared to reference devices synthesized at 450{\deg}C. Impedance spectroscopy confirms high recombination resistance and stable capacitance, linked to improved perovskite crystallinity. Our results highlight the potential of the RPAVD+SPE approach for producing low-temperature efficient ETLs, providing a feasible, industrially scalable, and eco-friendly alternative for manufacturing flexible, high-performance photovoltaic devices.

cond-mat.mtrl-sci

Mechanisms of de-icing by surface Rayleigh and plate Lamb acoustic waves

Acoustic waves (AW) have recently emerged as an energy-efficient ice removal procedure compatible with functional and industrial-relevant substrates. However, critical aspects at fundamental and experimental levels have yet to be disclosed to optimize their operational conditions. Identifying the processes and mechanisms by which different types of AWs induce de-icing are some of these issues. Herein, using model LiNbO3 systems and two types of interdigitated transducers, we analyze the de-icing and anti-icing efficiencies and mechanisms driven by Rayleigh surface acoustic waves (R-SAW) and Lamb waves with 120 and 510 um wavelengths, respectively. Through the experimental analysis of de-icing and active anti-icing processes and the finite element simulation of the AW generation, propagation, and interaction with small ice aggregates, we disclose that Lamb waves are more favorable than R-SAWs to induce de-icing and/or prevent the freezing of droplets. Prospects for applications of this study are supported by proof of concept experiments, including de-icing in an ice wind tunnel, demonstrating that Lamb waves can efficiently remove ice layers covering large LN substrates. Results indicate that the de-icing mechanism may differ for Lamb waves or R-SAWs and that the wavelength must be considered as an important parameter for controlling the efficiency.

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

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

Tailoring the Nucleation and Growth of Silver Nanoparticles by Sputtering Deposition under Acoustic Wave Activation. Assessment of Plasma Conditions and 2D Patterning Phenomena

Early results on the plasma deposition of dielectric thin films on acoustic wave (AW) activated substrates revealed a densification pattern arisen from the focusing of plasma ions and their impact on specific areas of the piezoelectric substrate. Herein, we extend this methodology to tailor the plasma deposition of metals onto AW-activated LiNbO3 piezoelectric substrates. Our investigation reveals the tracking of the initial stages of nanoparticle (NP) formation and growth during the submonolayer deposition of silver. We elucidate the specific role of AW activation in reducing particle size, enhancing particle circularity, and retarding NP agglomeration and account for the physical phenomena making these processes differ from those occurring on non-activated substrates. We provide a comparative analysis of the results obtained under two representative plasma conditions: diode DC sputtering and magnetron sputtering. In the latter case, the AW activation gives rise to a 2D pattern of domains with different amounts of silver and a distinct size and circularity for the silver NPs. This difference was attributed to the specific characteristics of the plasma sheath formed onto the substrate in each case. The possibilities of tuning the plasmon resonance absorption of silver NPs by AW activation of the sputtering deposition process are discussed.

physics.app-ph

Highly stable photoluminescence in vacuum-processed halide perovskite core-shell 1D nanostructures

Hybrid organometal halide perovskites (HP) present exceptional optoelectronic properties, but their poor long-term stability is a major bottleneck for their commercialization. Herein, we present a solvent-free approach to growing single-crystal organic nanowires (ONW), nanoporous metal oxide scaffolds, and HP to form a core@multishell architecture. The synthetic procedure is carried out under mild vacuum conditions employing thermal evaporation for the metal-free phthalocyanine (H2Pc) nanowires, which will be the core, plasma-enhanced chemical vapor deposition (PECVD) for the TiO2 shell, and co-evaporation of lead iodide (PbI2) and methylammonium iodide (CH3NH3I / MAI) for the CH3NH3PbI3 (MAPbI3 / MAPI) perovskite shell. We present a detailed characterization of the nanostructures by (S)-TEM and XRD, revealing a different crystallization of the hybrid perovskite depending on the template: while the growth on H2Pc nanowires induces the typical tetragonal structure of the MAPI perovskite, a low-dimensional phase (LDP) was observed on the one-dimensional TiO2 nanotubes. Such a combination yields an unprecedentedly stable photoluminescence emission over 20 hours and over 300 hours after encapsulation in polymethyl methacrylate (PMMA) under different atmospheres including N2, air, and high moisture levels. In addition, the unique one-dimensional morphology of the system, together with the high refractive index HP, allows for a strong waveguiding effect along the nanowire length.

physics.app-ph

Multidimensional nanoarchitectures for improved indoor light harvesting in dye-sensitized solar cells

Dye Sensitized Solar Cells (DSSCs) have recently regained attention for indoor light harvesting and powering wireless devices. Advantages such as cost-effectiveness, flexibility, wide angular response, and lightweight design have driven the fostering of the implementation of advanced photonic architectures, dedicated photosensitizers and compatibility with wearable carriers. However, to fully exploit their potential, crucial aspects require further attention, in particular the improvement of spectral compatibility and low-light harvesting mechanisms, as well as the development of efficient photoanodes through high-yield scalable methods. In this article, we propose the use of nanocomposite photoanodes integrating mesoporous TiO2 (m-TiO2) nanoparticles, ITO nanotubes (NTs) and TiO2 anatase shells (ITO@TiO2 NTs) prepared by step-by-step method relying on mild temperature conditions and avoiding toxic precursors. These photoanodes outperform previous attempts to implement low-dimensional ITO and ITO@TiO2 nanowires and nanotubes for outdoor light conversion, demonstrating an outstanding PCE under low artificial light intensity of 24 % for at 0.014 mWcm-2, a 166 % increase compared to the conventional architectures. Advanced microstructural, optical, and electrochemical characterizations have revealed that the strong scattering effect of the light in the visible range coupled with enhanced charge collection at low-intensity illumination are the essential mechanisms responsible for such enhanced energy conversion. Remarkably, our devices retain up to 90% of the normal incidence efficiency even under glancing illumination, while conventional reference devices show a drop down to 50%.

physics.app-ph

Conformal TiO$_2$ aerogel-like films by plasma deposition: from omniphobic antireflective coatings to perovskite solar cells photoelectrodes

The ability to control porosity in oxide thin films is one of the key factors that determine their properties. Despite the abundance of dry processes for the synthesis of oxide porous layers, the high porosity range is typically achieved by spin-coating-based wet chemical methods. Besides, special techniques such as supercritical drying are required to replace the pore liquid with air while maintaining the porous network. In this study, we propose a new method for the fabrication of ultra-porous titanium dioxide thin films at room or mild temperatures (T lower or equal to 120 degrees Celsius) by the sequential process involving plasma deposition and etching. These films are conformal to the substrate topography even for high-aspect-ratio substrates and show percolated porosity values above 85 percent that are comparable to advanced aerogels. The films deposited at room temperature are amorphous. However, they become partly crystalline at slightly higher temperatures presenting a distribution of anatase clusters embedded in the sponge-like structure. Surprisingly, the porous structure remains after annealing the films at 450 degrees Celsius in air, which increases the fraction of the embedded anatase nanocrystals. The films are antireflective, omniphobic, and photoactive becoming super-hydrophilic subjected to UV light irradiation The supported percolated nanoporous structure can be used as an electron-conducting electrode in perovskite solar cells. The properties of the cells depend on the aerogel film thickness reaching efficiencies close to those of commercial mesoporous anatase electrodes. This generic solvent-free synthesis is scalable and is applicable to ultra-high porous conformal oxides of different compositions with potential applications in photonics, optoelectronics, energy storage, and controlled wetting.

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

A holistic solution to icing by acoustic waves: de-icing, active anti-icing, sensing with piezoelectric crystals, and synergy with thin film passive anti-icing solutions

Icing has become a hot topic both in academia and in the industry given its implications in strategic sectors such as transport, robotics, wind turbines, photovoltaics, and electricity supply. Recently proposed de-icing solutions involving the propagation of acoustic waves (AWs) at suitable substrates may open the path for a sustainable alternative to standard de-icing or anti-icing protocols. Herein we experimentally unravel some of the basic interactions that contribute to the de-icing and/or hinder the icing (ice accretion) on AW-activated substrates. The response toward icing of a model substrate system consisting of a piezoelectric LiNbO3 plate AW activated by radio-frequency (rf) signaling to planar electrodes has been characterized both at a laboratory scale and in an icing wind tunnel under forced convection conditions. Main features related to de-icing mechanisms, a decrease of ice adhesion, or the avoidance of ice accretion have been disclosed by this holistic investigation. Furthermore, additional experiments have shown that the piezoelectric substrate surfaces modified with a fluorinated ZnO thin film or a ZnO/CFx bilayer present anti-icing functionality and a synergistic response when activated with AWs. A careful analysis of the dependence of resonance frequency of the piezoelectric substrates on experimental variables such as temperature, ice formation, or wind velocity shows that this parameter can be used as an internal control procedure for real-time monitoring of icing processes onto AW-activated devices

cond-mat.mtrl-sci

Ultrathin plasma polymer passivation of perovskite solar cells for improved stability and reproducibility

Despite the youthfulness of hybrid halide perovskite solar cells, their efficiencies are currently comparable to commercial silicon and have surpassed quantum-dots solar cells. Yet, the scalability of these devices is a challenge due to their low reproducibility and stability under environmental conditions. However, the methods reported to date to tackle such issues recurrently involve the use of solvent methods that would further complicate their transfer to industry. Herein we present a reliable alternative relaying in the implementation of an ultrathin plasma polymer as passivation interface between the electron transport material and the hybrid perovskite layer. Such nanoengineering interface provides solar devices with increased long-term stability under ambient conditions. Thus, without consideringr any additional encapsulation step, the cells retain more than 80 % of their efficiency after being exposed to the ambient atmosphere for more than 1000 h. Moreover, this plasma polymer passivation strategy significantly improves the coverage of the mesoporous scaffold by the perovskite layer, providing the solar cells with enhanced performance as well as improved reproducibility.

cond-mat.mtrl-sci

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