Host Matrix Materials for Luminescent Solar Concentrators: Recent Achievements and Forthcoming Challenges

Luminescent solar concentrators (LSCs) have attracted increasing attention in the past few years as appealing solar energy technology for the seamless integration of photovoltaic (PV) systems into the built environment. Traditionally, research in this field has focused on two main aspects: the optimization of the device assembly, in the quest for more efficient architectures to maximize collection, transport, and conversion of photons into usable electrical energy; the development of novel, highly emissive luminescent species, to ensure broad light collection and efficient photon emission. Only recently, the attention has also been directed toward the selection and development of suitable host matrix/waveguide materials with appropriate optical properties, sufficient chemical compatibility with the guest luminescent species, good processability for easy device fabrication and prolonged durability in outdoor operation. In addition to consolidated polymeric systems based on polyacrylates or polycarbonates, in recent years different examples of alternative host matrix systems have been proposed, characterized by peculiar chemical, physical and optical characteristics specifically designed to meet the stringent requirements of the LSC technology. This mini-review will focus on recent developments in the design of new host matrix materials for LSC applications. An overview of the most recent examples of novel LSC host matrices will be provided here, mainly focusing on new polymers, polymer-based organic-inorganic hybrids and multifunctional organic systems. Finally, opportunities and challenges in the field will be considered in view of the effective exploitation of the LSC technology in real application scenarios

Recent progress in encapsulation strategies to enhance the stability of organometal halide perovskite solar cells

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UV-Assisted 3D Printing of Glass and Carbon Fiber-Reinforced Dual-Cure Polymer Composites

Glass (GFR) and carbon fiber-reinforced (CFR) dual-cure polymer composites fabricated by UV-assisted three-dimensional (UV-3D) printing are presented. The resin material combines an acrylic-based photocurable resin with a low temperature (140 °C) thermally-curable resin system based on bisphenol A diglycidyl ether as base component, an aliphatic anhydride (hexahydro-4-methylphthalic anhydride) as hardener and (2,4,6,-tris(dimethylaminomethyl)phenol) as catalyst. A thorough rheological characterization of these formulations allowed us to define their 3D printability window. UV-3D printed macrostructures were successfully demonstrated, giving a clear indication of their potential use in real-life structural applications. Differential scanning calorimetry and dynamic mechanical analysis highlighted the good thermal stability and mechanical properties of the printed parts. In addition, uniaxial tensile tests were used to assess the fiber reinforcing effect on the UV-3D printed objects. Finally, an initial study was conducted on the use of a sizing treatment on carbon fibers to improve the fiber/matrix interfacial adhesion, giving preliminary indications on the potential of this approach to improve the mechanical properties of the 3D printed CFR components

Anthracene/tetracene cocrystals as novel fluorophores in thin-film luminescent solar concentrators

Efficient thin-film luminescent solar concentrators (LSCs) were fabricated using tetracene-doped anthracene cocrystals as novel fluorescent systems dispersed in a poly(methyl methacrylate) matrix. The LSC device efficiency ηLSC was found to reach 2.50%, with an optical efficiency ηopt in excess of 23% and a concentration factor C of 0.83%

The role of sol–gel chemistry in the low-temperature formation of ZnO buffer layers for polymer solar cells with improved performance

A new approach is proposed in this work to chemically control the low-temperature sol-gel formation of ZnO thin films used as efficient electron transporting layers (ETLs) in inverted polymer solar cells (PSCs). The chemical composition of the ZnO sol-gel precursor was modified by systematically employing different [H2O]/[Zn2+] molar ratios in the starting sol formulation and evaluating their influence on film properties and PSC device performance. A thorough characterization of the obtained ZnO ETLs evidenced the key importance of the [H2O]/[Zn2+] molar ratio to achieve effective control on the sol-gel hydrolysis and condensation processes. Based on these evidences, a mechanism for the formation of the ZnO films at the low processing temperatures used in this work was proposed. PSC devices were fabricated incorporating ZnO ETLs obtained from ZnO sol precursor formulations with increasing [H2O]/[Zn2+] ratios and their photovoltaic characterization revealed the presence of a maximum device efficiency for intermediate [H2O]/[Zn2+] values. Finally, the effect of water in the ZnO sol precursor on the long-term (>1000 h) shelf-life of PSCs fabricated onto flexible PET substrates was investigated and a correlation was found between chemical composition of the ZnO sol precursor and device shelf-life. The results of this study give a clear demonstration of a viable strategy to achieve improved PSC device performance by chemically controlling the formation of the sol-gel based ZnO ETL at processing temperatures compatible with flexible plastic substrates and provide useful guidelines for the development of efficient sol-gel derived metal-oxide buffer layers for highly performing flexible photovoltaics

Tuning the Properties of Biobased PU Coatings via Selective Lignin Fractionation and Partial Depolymerization

Polyurethane (PU) coatings with high lignin content and tunable properties were made using a combination of fractionation and partial catalytic depolymerization as a novel strategy to tailor lignin molar mass and hydroxyl group reactivity, the key parameters for use in PU coatings. Acetone organosolv lignin obtained from pilot-scale fractionation of beech wood chips was processed at the kilogram scale to produce lignin fractions with specific molar mass ranges (Mw 1000-6000 g/mol) and reduced polydispersity. Aliphatic hydroxyl groups were distributed relatively evenly over the lignin fractions, allowing detailed study of the correlation between lignin molar mass and hydroxyl group reactivity using an aliphatic polyisocyanate linker. As expected, the high molar mass fractions exhibited low cross-linking reactivity, yielding rigid coatings with a high glass transition temperature (Tg). The lower Mw fractions showed increased lignin reactivity, extent of cross-linking, and gave coatings with enhanced flexibility and lower Tg. Lignin properties could be further tailored by lignin partial depolymerization by reduction (PDR) of the beech wood lignin and its high molar mass fractions; excellent translation of the PDR process was observed from laboratory to the pilot scale necessary for coating applications in prospective industrial scenarios. Lignin depolymerization significantly improved lignin reactivity, and coatings produced from PDR lignin showed the lowest Tg values and highest coating flexibility. Overall, this study provides a powerful strategy for the production of PU coatings with tailored properties and high (>90%) biomass content, paving the path to the development of fully green and circular PU materials

Nonlinear optical properties of intriguing Ru σ-acetylide complexes and the use of a photocrosslinked polymer as a springboard to obtain SHG active thin films

This work reports on the design, synthesis and photo-physical properties of two ruthenium σ-alkynyl complexes. It is shown that, despite similar optical absorption features recorded in solution, the introduction of a benzaldehyde moiety leads to an improved non-linear optical (NLO) response as measured by Electric Field Induced Second Harmonic (EFISH) generation and Third Harmonic Generation (THG) at 1.907 μm, both related to the second order hyperpolarizability. These structure–property relationships are rationalized based on few state modelling. Complex 2 is subsequently processed to afford composite films that demonstrate a χ2 of 1.4 pm V−1, quite remarkable given the ease of film processing implemented in this work

Luminescent Downshifting by Photo-Induced Sol-Gel Hybrid Coatings: Accessing Multifunctionality on Flexible Organic Photovoltaics via Ambient Temperature Material Processing

A novel high-durability multifunctional organic-inorganic hybrid coating material is presented in this work as luminescent down-shifting (LDS) host matrix system for flexible organic photovoltaic (OPV) devices. Such new LDS coating is obtained by incorporating a convenient fluorescent organic dye in an appropriately functionalized fluoropolymeric resin that can be readily crosslinked by means of a dual-cure mechanism with a single-step ambient-temperature photo-induced sol-gel process. Due to its peculiar characteristics, the newly proposed system may be readily implemented in heat-sensitive flexible devices. By carefully tuning the amount of organic fluorophore in the hybrid coating material, a maximum increase in power conversion efficiency exceeding 4% is achieved on devices incorporating the new LDS layer with respect to control systems. This represents the highest efficiency enhancement reported to date on flexible OPVs by means of a polymer-based LDS layer. In addition, long-term accelerated weathering tests (>550 h) highlight the excellent stability of LDS-coated OPV devices, which can retain 80% of their initial performance, as opposed to the dramatic efficiency decay experienced by control uncoated devices. The approach presented here opens the way to the straightforward incorporation of versatile multifunctional light-managing layers on flexible OPV systems for improved device efficiency and lifetime

Polymeric materials for long-term durability of photovoltaic systems

Photovoltaic (PV) technology has evolved rapidly in the past few decades and now encompasses a large variety of materials and device structures. A key aspect to be taken into account in any PV technology is the operational durability of the systems in outdoor conditions. Clearly, loss of performance during operation represents a significant drawback and limitation in the commercialization of this technology. In this context, the large compositional flexibility of polymeric materials as well as their proven easy processability may be of great help in imparting improved durability to PV systems. In this review, a summary on the state of the art and most recent developments in the field of polymeric materials for improved long-term durability of PV devices is presented, with particular emphasis on the use of polymers as encapsulation materials and protective coatings in the field of both PV and light-concentration systems