Publications by authors named "Peter Siffalovic"

The development of new photochromic systems is motivated by the possibility of controlling the properties and functions of materials with high spatial and temporal resolution in a reversible manner. While there are several classes of photoswitches operating in solution, the design of systems efficiently operating in the solid state remains highly challenging, mainly due to limitations related to confinement effects. Triaryl-hydrazones represent a relatively new subclass of bistable hydrazone photoswitches exhibiting efficient / photochromism in solution.

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Although metal halide perovskites are positioned as the most powerful light-harvesting materials for sustainable energy conversion, there is a need for a thorough understanding of molecular design principles that would guide better engineering of organic hole-transporting materials, which are vital for boosting the performance and stability of perovskite solar cells. To address this formidable challenge, here, we developed a new design strategy based on the curved N-doped polycyclic aromatic hydrocarbon merged with T-shaped phenazines being decorated with (phenyl)-di--methoxyphenylamine (OMeTAD)─N-PAH23/24 and -3,6-ditertbutyl carbazole (TBCz)─N-PAH25/26. As N-PAH23/24 exhibited satisfying thermal stability, the comparative studies performed with various experimental and simulation methods revealed a pronounced correlation between the depth of the central cyclazine core and the form of the T-shape units.

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Article Synopsis
  • Interface engineering is vital for optimizing perovskite photovoltaics (PVs), focusing on reducing unwanted recombination to improve performance.
  • A novel approach involves creating a photo-ferroelectric perovskite interface by adding an ultrathin ferroelectric layer to enhance charge separation and reduce voltage losses.
  • This innovation has achieved a record open circuit voltage of 1.21 V and a champion efficiency of 24%, demonstrating a promising direction for advanced perovskite PV designs.
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Two bidentate ligands (L1 = 1-pentyl-2-(pyridin-2-yl)-1-benzimidazole and L2 = 1-heptyl-2-(pyridin-2-yl)-1-benzimidazole) were employed for the synthesis of five mononuclear Fe(II) coordination compounds 1-5 containing perchlorate, tetrafluoroborate and triflate counterions. Single-crystal X-ray diffraction analysis confirmed the expected molecular structures of all the reported compounds, revealing a moderately distorted octahedral geometry of {FeN} coordination chromophores. All five compounds exhibit thermal spin crossover with temperatures allocated above 400 K.

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At present, the power conversion efficiency of single-junction perovskite-based solar cells reaches over 26%. The further efficiency increase of perovskite-based optoelectronic devices is limited mainly by defects, causing the nonradiative recombination of charge carriers. To improve efficiency and ensure reproducible fabrication of high-quality layers, it is crucial to understand the perovskite nucleation and growth mechanism along with associated process control to reduce the defect density.

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The surface-enhanced Raman scattering (SERS) properties of low-dimensional semiconducting MXene nanoflakes have been investigated over the last decade. Despite this fact, the relationship between the surface characteristics and SERSing performance of a MXene layer has yet to be comprehensively investigated and elucidated. This work shows the importance of surface morphology on the overall SERS effect by studying few-layer TiCT MXene-based SERS substrates fabricated by vacuum-assisted filtration (VAF) and spray coating on filter paper.

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Photothermal therapy (PTT) mediated at the nanoscale has a unique advantage over currently used cancer treatments, by being spatially highly specific and minimally invasive. Although PTT combats traditional tumor treatment approaches, its clinical implementation has not yet been successful. The reasons for its disadvantage include an insufficient treatment efficiency or low tumor accumulation.

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Solid-state batteries have the potential to replace the current generation of liquid electrolyte batteries. However, the major limitation resulting from their solid-state architecture is the gradual loss of ionic conductivity due to the loss of physical contact between the individual battery components during charging/discharging. This is mainly due to mechanical stresses caused by volume changes in the cathode and anode during lithiation and delithiation.

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Currently, two approaches dominate the large-scale production of MoS: liquid-phase exfoliation, referred to as the top-down approach, and bottom-up colloidal synthesis from molecular precursors. Known colloidal synthesis approaches utilize toxic precursors. Here, an alternative green route for the bottom-up synthesis of MoS nanoflakes (NFs) is described.

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Article Synopsis
  • - Molybdenum disulfide (MoS) few-layer films are being investigated for their potential use in electronics, optics, and energy applications, especially when intercalated with alkali metals like lithium.
  • - This study explores how lithium affects MoS film properties, using a novel method that incorporates lithium during the film's formation, resulting in improved growth and alignment.
  • - The findings reveal that lithium not only promotes the growth and horizontal alignment of MoS films but also causes a significant change in orientation from vertical to horizontal, with the Li-doped films showing long-term stability and maintained chemical composition.
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Nanoparticle superlattices produced with controllable interparticle gap distances down to the subnanometer range are of superior significance for applications in electronic and plasmonic devices as well as in optical metasurfaces. In this work, a method to fabricate large-area (∼1 cm) gold nanoparticle (GNP) superlattices with a typical size of single domains at several micrometers and high-density nanogaps of tunable distances (from 2.3 to 0.

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The biocolonization of building materials by microorganisms is one of the main causes of their degradation. Fungi and bacteria products can have an undesirable impact on human health. The protection and disinfection of sandstone and wood materials are of great interest.

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The efficiency of perovskite-based solar cells has increased dramatically over the past decade to as high as 25%, making them very attractive for commercial use. Vapor deposition is a promising technique that potentially enables fabrication of perovskite solar cells on large areas. However, to implement a large-scale deposition method, understanding and controlling the specific growth mechanisms are essential for the reproducible fabrication of high-quality layers.

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The few-layer transition metal dichalcogenides (TMD) are an attractive class of materials due to their unique and tunable electronic, optical, and chemical properties, controlled by the layer number, crystal orientation, grain size, and morphology. One of the most commonly used methods for synthesizing the few-layer TMD materials is the chemical vapor deposition (CVD) technique. Therefore, it is crucial to develop in situ inspection techniques to observe the growth of the few-layer TMD materials directly in the CVD chamber environment.

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The assembly of nanomaterials into thin films is an important area in the nanofabrication of novel devices. The monodispersity of nanoparticles plays an essential role in the resulting quality of the assembled mono- and multilayers. Larger polydispersity leads to smaller lateral correlation lengths and smaller domains of aligned nanoparticles, thus resulting in more point and line defects.

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Unique structure and ability to control the surface termination groups of MXenes make these materials extremely promising for solid lubrication applications. Due to the challenging delamination process, the tribological properties of two-dimensional MXenes particles have been mostly investigated as additive components in the solvents working in the macrosystem, while the understanding of the nanotribological properties of mono- and few-layer MXenes is still limited. Here, we investigate the nanotribological properties of mono- and double-layer TiCT MXenes deposited by the Langmuir-Schaefer technique on SiO/Si substrates.

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The synergistic effect of high-quality NiOhole transport layers (HTLs) deposited by ion beam sputtering on ITO substrates and the TiCTMXene doping of CHNHPbI(MAPI) perovskite layers is investigated in order to improve the power conversion efficiency (PCE) of p-i-n perovskite solar cells (PSCs). The 18 nm thick NiOlayers are pinhole-free and exhibit large-scale homogeneous surface morphology as revealed by the atomic force microscopy (AFM). The grazing-incidence x-ray diffraction showed a 0.

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Hypothesis: One of the highlighted properties of TiCT MXene compared to other 2D nanomaterials is its hydrophilicity. However, the broad range of static contact angles of TiCT reported in the literature is misleading. To elucidate the experimental values of the static contact angles and get reproducible contact angle data, it is wiser to perform the advancing and receding contact angle measurements on smooth and compact TiCT layers and focus on deep understanding of the physical basis behind the wettability, which is provided by contact angle hysteresis.

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Electronic devices based on polymer thin films have experienced a tremendous increase in their efficiency in the last two decades. One of the critical factors that affects the efficiency of polymer solar cells or light emitting devices is the presence of structural defects that controls non-radiative recombination. The purpose of this report is to demonstrate a non-trivial thickness dependence of optoelectronic properties and structure (dis)order in thin conductive poly(9,9-dioctyfluorene-alt-benzothiadiazole), F8BT, polymer films.

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Thin films of transition-metal dichalcogenides are potential materials for optoelectronic applications. However, the application of these materials in practice requires knowledge of their fundamental optical properties. Many existing methods determine optical constants using predefined models.

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Article Synopsis
  • Lead-halide perovskites are gaining traction in solar cells and optoelectronics because they are achieving higher power conversion efficiencies, rivaling traditional inorganic semiconductors.
  • To further enhance their performance, it's essential to understand and reduce the defects that cause nonradiative recombination of charge carriers.
  • This study focuses on analyzing the crystallization process of MAPbICl perovskite during thermal annealing using photoluminescence spectroscopy and GIWAXS to track defects and phase transitions in real-time.
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Acute myeloid leukemia (AML) is a highly aggressive type of cancer caused by the uncontrolled proliferation of undifferentiated myeloblasts, affecting the bone marrow and blood. Systemic chemotherapy is considered the primary treatment strategy; unfortunately, healthy cells are also affected to a large extent, leading to severe side effects of this treatment. Targeted drug therapies are becoming increasingly popular in modern medicine, as they bypass normal tissues and cells.

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Thermoresponsive polymers play an important role in designing drug delivery systems for biomedical applications. In this contribution, the effect of encapsulated hydrophobic drug dexamethasone on thermoresponsive behavior of diblock copolymers was studied. A small series of diblock copoly(2-oxazoline)s was prepared by combining thermoresponsive 2--propyl-2-oxazoline (PrOx) and hydrophilic 2-methyl-2-oxazoline (MeOx) in two ratios and two polymer chain lengths.

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Many polymorphic crystal structures of copper phthalocyanine (CuPc) have been reported over the past few decades, but despite its manifold applicability, the structure of the frequently mentioned α polymorph remained unclear. The base-centered unit cell (space group 2/) suggested in 1966 was ruled out in 2003 and was replaced by a primitive triclinic unit cell (space group 1). This study proves unequivocally that both α structures coexist in vacuum-deposited CuPc thin films on native silicon oxide by reciprocal space mapping using synchrotron radiation in grazing incidence.

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Gel filtration is a versatile technique employed for biological molecules and nanoparticles, offering their reproducible classification based on size and shape. Colloidal nanoparticles are of significant interest in biomedical applications due to a large number of solution-based bioconjugation procedures. Nevertheless, the inherent polydispersity of the nanoparticles produced by various techniques necessitates the employment of high yield separation and purification techniques.

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