Can Impurities be Beneficial to Photovoltaics?

The state of the art of the intermediate band solar cells is presented with emphasis on the use of impurities or alloys to form bulk intermediate band materials. Quantum dot intermediate band solar cells start to present already attractive efficiencies but many difficulties jeopardize the immediate achievement of record efficiency cells. To complement this research it is worthwhile examining bulk materials presenting an IB. Four or perhaps more materials have already proven to have it and several paths for the research of more are today open but no solar cell has yet been published based on them. This topic has already attracted many researches and abundant funds for their development worldwide

Luminescence in sulfides : a rich history and a bright future

Sulfide-based luminescent materials have attracted a lot of attention for a wide range of photo-, cathodo- and electroluminescent applications. Upon doping with Ce3+ and Eu2+, the luminescence can be varied over the entire visible region by appropriately choosing the composition of the sulfide host. Main application areas are flat panel displays based on thin film electroluminescence, field emission displays and ZnS-based powder electroluminescence for backlights. For these applications, special attention is given to BaAl2S4:Eu, ZnS:Mn and ZnS:Cu. Recently, sulfide materials have regained interest due to their ability (in contrast to oxide materials) to provide a broad band, Eu2+-based red emission for use as a color conversion material in white-light emitting diodes (LEDs). The potential application of rare-earth doped binary alkaline-earth sulfides, like CaS and SrS, thiogallates, thioaluminates and thiosilicates as conversion phosphors is discussed. Finally, this review concludes with the size-dependent luminescence in intrinsic colloidal quantum dots like PbS and CdS, and with the luminescence in doped nanoparticles

An Efficient Synthesis and Photoelectric Properties of Green Carbon Quantum Dots with High Fluorescent Quantum Yield

© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)To greatly improve the production quality and efficiency of carbon quantum dots (CQDs), and provide a new approach for the large-scale production of high-quality CQDs, green carbon quantum dots (g-CQDs) with high product yield (PY) and high fluorescent quantum yield (QY) were synthesized by an efficient one-step solvothermal method with 2,7-dihydroxynaphthalene as the carbon source and ethylenediamine as the nitrogen dopant in this study. The PY and QY of g-CQDs were optimised by adjusting reaction parameters such as an amount of added ethylenediamine, reaction temperature, and reaction duration. The results showed that the maximum PY and QY values of g-CQDs were achieved, which were 70.90% and 62.98%, respectively when the amount of added ethylenediamine, reaction temperature, and reaction duration were 4 mL, 180 °C, and 12 h, respectively. With the optimised QY value of g-CQDs, white light emitting diodes (white LEDs) were prepared by combining g-CQDs and blue chip. The colour rendering index of white LEDs reached 87, and the correlated colour temperature was 2520 K, which belongs to the warm white light area and is suitable for indoor lighting. These results indicate that g-CQDs have potential and wide application prospects in the field of white LEDs.Peer reviewedFinal Published versio

Structure–property insights into nanostructured electrodes for Li-ion batteries from local structural and diffusional probes

Microwave heating presents a faster, lower energy synthetic methodology for the realization of functional materials. Here, we demonstrate for the first time that employing this method also leads to a decrease in the occurrence of defects in olivine structured LiFe1−xMnxPO4. For example, the presence of antisite defects in this structure precludes Li+ diffusion along the b-axis leading to a significant decrease in reversible capacities. Total scattering measurements, in combination with Li+ diffusion studies using muon spin relaxation (μ+SR) spectroscopy, reveal that this synthetic method generates fewer defects in the nanostructures compared to traditional solvothermal routes. Our interest in developing these routes to mixed-metal phosphate LiFe1−xMnxPO4 olivines is due to the higher Mn2+/3+ redox potential in comparison to the Fe2+/3+ pair. Here, single-phase LiFe1−xMnxPO4 (x = 0, 0.25, 0.5, 0.75 and 1) olivines have been prepared following a microwave-assisted approach which allows for up to 4 times faster reaction times compared to traditional solvothermal methods. Interestingly, the resulting particle morphology is dependent on the Mn content. We also examine their electrochemical performance as active electrodes in Li-ion batteries. These results present microwave routes as highly attractive for reproducible, gram-scale syntheses of high quality nanostructured electrodes which display close to theoretical capacity for the full iron phase

The Comparison of Characteristics in Tin Doped Indium Oxide (ITO) Synthesized via Nonaqueous Sol-Gel and Solvothermal Process

Tin doped indium oxide nanoparticles were synthesized by nonaqueous sol-gel method and solvothermal process from indium acetylacetonate (In(acac)3) and tin bis(acetylacetonate)dichloride (Sn(acac)2Cl2) in oleyamine as the starting materials. The structure and morphology of ITO samples were analyzed by XRD and TEM. The electrical conductivy and specific surface area of both ITO samples were also determined and compared to each other. The ITO prepared via solvothermal method showed better results that prepared by nonaqueous sol-gel method

Functionalisation of colloidal transition metal sulphides nanocrystals: A fascinating and challenging playground for the chemist

Metal sulphides, and in particular transition metal sulphide colloids, are a broad, versatile and exciting class of inorganic compounds which deserve growing interest and attention ascribable to the functional properties that many of them display. With respect to their oxide homologues, however, they are characterised by noticeably different chemical, structural and hence functional features. Their potential applications span several fields, and in many of the foreseen applications (e.g., in bioimaging and related fields), the achievement of stable colloidal suspensions of metal sulphides is highly desirable or either an unavoidable requirement to be met. To this aim, robust functionalisation strategies should be devised, which however are, with respect to metal or metal oxides colloids, much more challenging. This has to be ascribed, inter alia, also to the still limited knowledge of the sulphides surface chemistry, particularly when comparing it to the better established, though multifaceted, oxide surface chemistry. A ground-breaking endeavour in this field is hence the detailed understanding of the nature of the complex surface chemistry of transition metal sulphides, which ideally requires an integrated experimental and modelling approach. In this review, an overview of the state-of-the-art on the existing examples of functionalisation of transition metal sulphides is provided, also by focusing on selected case studies, exemplifying the manifold nature of this class of binary inorganic compounds

Defect chemistry and vacancy concentration of luminescent europium doped ceria nanoparticles by solvothermal method

Pure phase and europium-doped ceria nanocrystals have been synthesized by a single step simple solvothermal process. Different spectroscopic, diffractive, and microscopic techniques were used to determine the morphology, size, crystal structure, and phase of all the samples. Electron energy loss spectroscopy (EELS) for elemental mapping confirmed that good solid solutions were formed and that the particles had a homogeneous distribution of europium. The defect chemistry was more complex than might be expected with the incorporation of each Eu3+ ion resulting in the production of an anion vacancy since the doping results in charge compensating (i.e., for Eu3+) anion vacancies as well as vacancies due to oxygen removal from the crystallite surface. Variations in nanoparticles dimension and lattice parameters were measured as a function of dopant concentrations and their variations explained. The band gap of the samples could be tailored by the doping. The doped samples were found to be luminescent due to the substitution of Ce4+ ions in the cubic symmetric lattice by the dopant ions. The thermal stability of the fluorescence properties was also investigated