Ugur Deneb Menda

This work presents an optimisation study of silicon surface preparation for silicon heterojunction solar cells (SHJ) fabricated from surface-damaged wafers, aiming to ensure minimal surface defects and improved passivation at the crystalline silicon-hydrogenated amorphous silicon (c-Si/a-Si:H) interface. KOH etching conditions were optimized to remove diamond‑wire‑saw (DWS) damage on c‑Si while tuning nanoscale faceting for improved interface passivation. Namely, KOH 45% was used to smooth the surface and remove saw damage, while KOH 5% generated approximately 20 nm pyramidal‑like features in a single‑step, IPA‑free process. For the fabrication of SHJ solar cells with an Aluminium Back Surface Field (Al-BSF), intrinsic and n-type doped a-Si:H layers were deposited by plasma-enhanced chemical vapor deposition (PECVD) on the front side of the devices. Two different (i)a-Si:H films, one dense, deposited with 50% hydrogen dilution, (id)a-Si:H, and the other, under-dense, using pure silane gas, (iud)a-Si:H, were used in different solar cells. A relative improvement of 18% in implied PCE (Suns‑Voc) was observed for KOH 5% with dense (id)a‑Si:H versus KOH 45%, which was attributed to the effect of nanoscale faceting created on the c‑Si surface by the 5% KOH treatment.

Maximizing solar cell efficiency is a critical step toward revolutionizing photovoltaic technologies and harnessing the full potential of light for energy conversion. This study investigates the incorporation of NaGdF₄:Yb³⁺,Tm³⁺@NaGdF₄:Eu³⁺ (TMN) and NaGdF₄:Yb³⁺,Er³⁺@NaGdF₄:Eu³⁺ (ERN) nanoparticles into perovskite solar cells (PSCs) to improve their power conversion efficiency. The nanoparticles were synthesized through thermolysis and characterized using multiple techniques, including photoluminescence spectroscopy, quantum yield measurements, transmission electron microscopy, X-ray diffraction, solar simulation, and external quantum efficiency assessments. These lanthanide-doped NPs exhibited strong downshifting and minor upconversion luminescence, acting like optical translators that reshape poorly absorbed light into usable wavelengths. Devices incorporating the ERN nanoparticles demonstrated a 22.19% relative increase in power conversion efficiency, while those with TMN showed a 13.23% improvement. These enhancements are attributed mainly to the effective downshifting emission of Eu³⁺ and improved surface passivation from the core–shell architecture, which together reduce recombination losses and improve charge carrier dynamics. These findings underscore the potential of photon-converting lanthanide-based materials to address spectral absorption limitations in PSCs, offering a promising route toward next-generation photovoltaic technologies.

By taking advantage of the outstanding intrinsic optoelectronic properties of perovskite-based photovoltaic materials, together with the strong near-infrared (NIR) absorption and electronic confinement in PbS quantum dots (QDs), sub-bandgap photocurrent generation is possible, opening the way for solar cell efficiencies surpassing the classical limits. The present study shows an effective methodology for the inclusion of high densities of colloidal PbS QDs in a MAPbI₃ (methylammonium lead iodide) perovskite matrix as a means to enhance the spectral window of photon absorption of the perovskite host film and allow photocurrent production below its bandgap. The QDs were introduced in the perovskite matrix in different sizes and concentrations to study the formation of quantum-confined levels within the host bandgap and the potential formation of a delocalized intermediate mini-band (IB). Pronounced sub-bandgap (in NIR) absorption was optically confirmed with the introduction of QDs in the perovskite. The consequent photocurrent generation was demonstrated via photoconductivity measurements, which indicated IB establishment in the films. Despite verifying the reduced crystallinity of the MAPbI₃ matrix with a higher concentration and size of the embedded QDs, the nanostructured films showed pronounced enhancement (above 10-fold) in NIR absorption and consequent photocurrent generation at photon energies below the perovskite bandgap.

Advanced light management via front‐coated photonic nanostructures is a promising strategy to enhance photovoltaic (PV) efficiency through wave‐optical light‐trapping (LT) effects, avoiding the conventional texturing processes that induce the degradation of electrical performance due to increased carrier recombination. Titanium dioxide (TiO₂) honeycomb arrays with different geometry are engineered through a highly‐scalable colloidal lithography method on flat crystalline silicon (c‐Si) wafers and tested on standard planar c‐Si interdigitated back‐contact solar cells (pIBCSCs). The photonic‐structured wafers achieve an optical photocurrent of 36.6 mA cm⁻², mainly due to a broad anti‐reflection effect from the 693 nm thick nanostructured coatings. In contrast, the pIBCSC test devices reach 14% efficiency with 679 nm thick TiO₂ nanostructures, corresponding to a ≈30% efficiency gain relative to uncoated pIBCSCs. In addition, several designed structures show unmatched angular acceptance enhancements in efficiency (up to 63% gain) and photocurrent density (up to 68% gain). The high‐performing (yet electrically harmless) LT scheme, here presented, entails an up‐and‐coming alternative to conventional texturing for c‐Si technological improvement that can be straightforwardly integrated into the established PV industry.

The sheltered environment of the Algares +30 level adit (underground mine gallery) contributes to the preservation of secondary water-soluble minerals formed on the tunnel walls. The massive sulphide and related stockwork zone are hosted by the Mine Tuff volcanic unit and are exposed in the walls of the gallery, showing intense oxidation and hydrothermal alteration. Minerals from the halotrichite group were identified on the efflorescent salts, typically white fine-acicular crystals but also on aggregates with dark orange/brownish colour. Mineral characterization was performed using several methods and analytical techniques (XRD, XRF-WDS, SEM-EDS, DTA-TG), and the chemical formulas were calculated maintaining the ratio A:B ≅ 1:2 in accordance with the general formula of the halotrichite group, AB₂(SO₄)₄·22H₂O. This methodology allowed the assignment of the orange colour to the presence of trivalent iron on iron-rich pickeringite in partial substitution of aluminium.

Poly(hydroxyalkanoates) (PHAs) with different material properties, namely, the homopolymer poly(3-hydroxybutyrate), P(3HB), and the copolymer poly(3-hydroxybutyrate-co-3-hydroxyvalerate, P(3HB-co-3HV), with a 3HV of 25 wt.%, were used for the preparation of porous biopolymeric scaffolds. Solvent casting with particulate leaching (SCPL) and emulsion templating were evaluated to process these biopolymers in porous scaffolds. SCPL scaffolds were highly hydrophilic (>170% swelling in water) but fragile, probably due to the increase of the polymer’s polydispersity index and its high porosity (>50%). In contrast, the emulsion templating technique resulted in scaffolds with a good compromise between porosity (27–49% porosity) and hydrophilicity (>30% water swelling) and without impairing their mechanical properties (3.18–3.35 MPa tensile strength and 0.07–0.11 MPa Young’s Modulus). These specifications are in the same range compared to other polymer-based scaffolds developed for tissue engineering. P(3HB-co-3HV) displayed the best overall properties, namely, lower crystallinity (11.3%) and higher flexibility (14.8% elongation at break. Our findings highlight the potency of our natural biopolyesters for the future development of novel porous scaffolds in tissue engineering, thanks also to their safety and biodegradability.

Lead-halide perovskite solar cells (PSCs) are currently the most promising emergent thin-film photovoltaic technology, having already reached power conversion efficiency (PCE) levels of state-of-the-art wafer-based silicon cells. The class of wide bandgap PSCs has also demonstrated high PCE values, thus becoming highly attractive for top sub-cells in tandem devices constructed with silicon or other types of bottom sub-cells. In this study, wide bandgap double-halide (Cs_0.17FA_0.83PbI_3−xBr_x) perovskite absorbers were developed with different bromine content, aiming to obtain bandgap values between 1.66 to 1.74 eV, by a glovebox-free (ambient) procedure. Low-cost inorganic materials, i.e. TiO₂ and CuSCN, were used for the electron and hole transport layers, respectively. The 1.70 eV bandgap perovskite resulted in the highest reproducibility and stability (>80% initial PCE after 3500 hours) properties of the PSCs, remarkably attaining 16.4% PCE even with ambient and high humidity (∼70%) fabrication conditions.

Poly(hydroxyalkanoates) (PHAs) with differing material properties, namely, the homopolymer poly(3-hydroxybutyrate), P(3HB), the copolymer poly(3-hydroxybutyrate-co-3-hydroxyvalerate), P(3HB-co-3HV), with a 3HV content of 25 wt.% and a medium chain length PHA, and mcl-PHA, mainly composed of 3-hydroxydecanoate, were studied as scaffolding material for cell culture. P(3HB) and P(3HB-co-3HV) were individually spun into fibers, as well as blends of the mcl-PHA with each of the scl-PHAs. An overall biopolymer concentration of 4 wt.% was used to prepare the electrospinning solutions, using chloroform as the solvent. A stable electrospinning process and good quality fibers were obtained for a solution flow rate of 0.5 mL h⁻¹, a needle tip collector distance of 20 cm and a voltage of 12 kV for P(3HB) and P(3HB-co-3HV) solutions, while for the mcl-PHA the distance was increased to 25 cm and the voltage to 15 kV. The scaffolds’ hydrophilicity was significantly increased under exposure to oxygen plasma as a surface treatment. Complete wetting was obtained for the oxygen plasma treated scaffolds and the water uptake degree increased in all treated scaffolds. The biopolymers crystallinity was not affected by the electrospinning process, while their treatment with oxygen plasma decreased their crystalline fraction. Human dermal fibroblasts were able to adhere and proliferate within the electrospun PHA-based scaffolds. The P(3HB-co-3HV): mcl-PHA oxygen plasma treated scaffold highlighted the most promising results with a cell adhesion rate of 40 ± 8%, compared to 14 ± 4% for the commercial oxygen plasma treated polystyrene scaffold Alvetex^TM. Scaffolds based on P(3HB-co-3HV): mcl-PHA blends produced by electrospinning and submitted to oxygen plasma exposure are therefore promising biomaterials for the development of scaffolds for tissue engineering.

Amorphous/crystalline silicon interfaces feature considerably larger valence than conduction band offsets. In this article, we analyze the impact of such band offset asymmetry on the performance of silicon heterojunction solar cells. To this end, we use silicon suboxides as passivation layers—inserted between substrate and (front or rear) contacts—since such layers enable intentionally exacerbated band-offset asymmetry. Investigating all topologically possible passivation layer permutations and focussing on light and dark current-voltage characteristics, we confirm that to avoid fill factor losses, wider-bandgap silicon oxide films (of at least several nanometer thin) should be avoided in hole-collecting contacts. As a consequence, device implementation of such films as window layers—without degraded carrier collection—demands electron collection at the front and hole collection at the rear. Furthermore, at elevated operating temperatures, once possible carrier transport barriers are overcome by thermionic (field) emission, the device performance is mainly dictated by the passivation of its surfaces. In this context, compared to the standard amorphous silicon layers, the wide-bandgap oxide layers applied here passivate remarkably better at these temperatures, which may represent an additional benefit under practical operation conditions.