The important role of Cuprous thiocyanate

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Understanding of perovskite crystal growth and film formation in scalable deposition processes

Hybrid organic-inorganic perovskite photovoltaics (PSCs) have attracted significant attention during the past decade. Despite the stellar rise of laboratory-scale PSC devices, which have reached a certified efficiency over 25% to date, there is still a large efficiency gap when transiting from small-area devices to large-area solar modules. Efficiency losses would inevitably arise from the great challenges of homogeneous coating of large-area high quality perovskite films. To address this problem, we provide an in-depth understanding of the perovskite nucleation and crystal growth kinetics, including the LaMer and Ostwald ripening models, which advises us that fast nucleation and slow crystallization are essential factors in forming high-quality perovskite films. Based on these cognitions, a variety of thin film engineering approaches will be introduced, including the anti-solvent, gas-assisted and solvent annealing treatments, Lewis acid-base adduct incorporation, etc., which are able to regulate the nucleation and crystallization steps. Upscaling the photovoltaic devices is the following step. We summarize the currently developed scalable deposition technologies, including spray coating, slot-die coating, doctor blading, inkjet printing and vapour-assisted deposition. These are more appealing approaches for scalable fabrication of perovskite films than the spin coating method, in terms of lower material/solution waste, more homogeneous thin film coating over a large area, and better morphological control of the film. The working principles of these techniques will be provided, which direct us that the physical properties of the precursor solutions and surface characteristics/temperature of the substrate are both dominating factors influencing the film morphology. Optimization of the perovskite crystallization and film formation process will be subsequently summarized from these aspects. Additionally, we also highlight the significance of perovskite stability, as it is the last puzzle to realize the practical applications of PSCs. Recent efforts towards improving the stability of PSC devices to environmental factors are discussed in this part. In general, this review, comprising the mechanistic analysis of perovskite film formation, thin film engineering, scalable deposition technologies and device stability, provides a comprehensive overview of the current challenges and opportunities in the field of PSCs, aiming to promote the future development of cost-effective up-scale fabrication of highly efficient and ultra-stable PSCs for practical applications.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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High-Performance P-Type Copper(I) Thiocyanate Thin Film Transistors Processed from Solution at Low Temperature

Semiconducting copper(I) thiocyanate (CuSCN) is actively studied for electronic and optoelectronic applications. Although various kinds of CuSCN-based transistors are reported, these devices suffer from low charge carrier mobility of about 0.01?0.1 cm2 V?1 s?1. Here, ion gel electrolyte consisting of network polymer and ionic liquid is used as a high capacitance gate insulator to achieve high performance CuSCN-based electrolyte-gated transistors (CuSCN-EGTs) with low operation voltage below 1 V. 30 nm thick CuSCN semiconductor film can be formed by a simple solution process with a low processing temperature (?100 C) that is directly applicable to flexible plastic substrates. By doping copper iodide to the CuSCN semiconductor, device performance including drain current and charge carrier mobility of the CuSCN EGT can be improved significantly. The measured charge carrier mobility of ?0.3 cm2 V?1 s?1 is the highest among the reported CuSCN transistors using various gate insulators. These CuSCN-EGTs also display good operation stability under continuous quasistatic external gate voltage sweeps. Such superior electrical performance and versatile processability of ion gel?gated CuSCN transistors make them suitable for use in complimentary circuits and large-area flexible electronics.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Because a catalyst decreases the height of the energy barrier, 1111-67-7, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1111-67-7, Name is Cuprous thiocyanate, molecular formula is CCuNS. In a article£¬once mentioned of 1111-67-7

Toward Long-Term Stable and Highly Efficient Perovskite Solar Cells via Effective Charge Transporting Materials

Perovskite solar cells (PSCs) have advanced quickly with their power conversion efficiency approaching the record of silicon solar cells. However, there is still a big challenge to obtain both high efficiency and long-term stability for future commercialization of PSCs. The major instability issue is associated with the decomposition or phase transition of perovskite materials that are believed to be intrinsically unstable under outdoor working conditions. Herein, the authors review the approaches that marked important progress in developing new functional electron/hole transporting materials that enabled highly efficient and stable PSCs. The findings that accelerate charge diffusion and that suppress the irrevocable loss of ions diffusing out of perovskite materials and other diffusion processes are highlighted. In addition, derivative interface engineering methods to control the diffusion process of charges/ions/molecules are also reviewed. Finally, the authors propose key research issues in charge transporting materials and interface engineering with regard to the important diffusion processes that will be one of the keys to realize highly efficient and long-term stable PSCs.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Extended knowledge of Cuprous thiocyanate

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The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.1111-67-7, Name is Cuprous thiocyanate, molecular formula is CCuNS, 1111-67-7. In a Article, authors is Tennakone£¬once mentioned of 1111-67-7

DYE SENSITIZATION OF CUPROUS THIOCYANATE PHOTOCATHODE IN AQUEOUS KCNS.

Cuprous thiocyanate (p-type semiconductor) is found to adsorb thiocyanated cationic dyes to yield high photo-responses in aqueous KCNS. The method of preparation and the performance of dye-sensitized CuCNS photocathodes are discussed.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. 1317-39-1, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 1317-39-1, name is Copper(I) oxide. In an article£¬Which mentioned a new discovery about 1317-39-1

N2O decomposition over CuO/CeO2 catalyst: New insights into reaction mechanism and inhibiting action of H2O and NO by operando techniques

In this work, a combination of ex situ (STEM-EELS, STEM-EDX, H2-TPR and XPS), in situ (CO-DRIFTS) and operando (DR UV?vis and DRIFTS) approaches was used to probe the active sites and determine the mechanism of N2O decomposition over highly active 4?wt.% Cu/CeO2 catalyst. In addition, reaction pathways of catalyst deactivation in the presence of NO and H2O were identified. The results of operando DR UV?vis spectroscopic tests suggest that [Cu?O?Cu]2+ sites play a crucial role in catalytic N2O decomposition pathway. Due to exposure of {1?0?0} and {1?1?0} high-energy surface planes, nanorod-shaped CeO2 support simultaneously exhibits enhancement of CuO/CeO2 redox properties through the presence of Ce3+/Ce4+ redox pair. Its dominant role of binuclear Cu+ site regeneration through the recombination and desorption of molecular oxygen is accompanied by its minor active participation in direct N2O decomposition. NO and H2O have completely different inhibiting action on the N2O decomposition reaction. Water molecules strongly and dissociatively bind to oxygen vacancy sites of CeO2 and block further oxygen transfer as well as regeneration of catalyst active sites. On the other hand, the effect of NO is expressed through competitive oxidation to NO2, which consumes labile oxygen from CeO2 and decelerates [Cu+ Cu+] active site regeneration.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Copper-Mediated [(Diethylphosphono)difluoromethyl]thiolation of alpha-Bromo Ketones

We report herein a straightforward access to alpha-[(diethoxyphosphoryl)difluoromethyl]thiolated ketones. The methodology, which involves the nucleophilic [Cu]CF2PO(OEt)2 species, has allowed the formation of the targeted compounds in moderate to high yields by using a simple procedure. This method represents a convenient alternative to the known approaches for the introduction of this emergent fluorinated motif.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Final Thoughts on Chemistry for Bis(acetylacetone)copper

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. 13395-16-9, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 13395-16-9, name is Bis(acetylacetone)copper. In an article£¬Which mentioned a new discovery about 13395-16-9

Copper-Catalyzed Oxidative Self-Coupling of alpha-Amino Carbonyl Compounds for the Synthesis of Tetrasubstituted 1,4-Enediones

A protocol for the copper-catalyzed oxidative self-coupling of alpha-amino carbonyl compounds has been developed for the synthesis of tetrasubstituted 1,4-enediones (Z -isomers) in moderate to good yields through the cleavage of four sp 3 C-H bonds and the simultaneous formation of one C=C double bond in the alpha-amino carbonyl compound. The strategy has the advantages of using readily available starting materials and of high stereoselectivity.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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X-ray determination of effective charges on sulphur, phosphorus, silicon and chlorine atoms

The values of Kalpha line shifts of A atoms (A=S, P, Si, Cl) for 500 sulphur compounds, 206 phosphorus compounds, 52 silicon compounds and 129 chlorine compounds are reported.The connection between AKalpha shifts and effective charges on A atom is discussed.The substantial degree of linearity in this relationship is shown by semiempirical and empirical methods of calculation.Some regularities of the electron structure of A-containing compounds have been established.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Reactions of alpha,beta-Enones with Diazo Compounds: Part 4: Reaction Pathways from (Z)- and (E)-alpha,beta-Enones with Dimethyl Diazomalonate

In this study, (E)- and (Z)-enones carrying only a phenyl substituent at their C(beta) atom were treaced with dimethyl diazomalonate in the presence of (acetylacetonato)copper(II). According to the configuration of the starting enones, the products were dioxole or dihydrofuran derivatives, significant heterocycles in natural products.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

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Oxadiazole and oxadiazoline derivatives

There are described new compounds of formula STR1 in which E is selected from the group consisting of residues of formula STR2 in which R” is selected from the group consisting of amino, vinyl, allyl, ethynyl, C1 -C5 alkyl, C1 -C5 alkoxy, or C1 -C5 alkylthio or a C1 -C5 alkyl group susbstituted by at least one halogen atom; and hydrogen; in which R1 and R2 are each selected from the group consisting of hydrogen, halogen, methyl and ethyl; and R’ is selected from substituted phenyl when R” is other than hydrogen, and phenyl, thienyl and substituted phenyl and thienyl when R” is hydrogen. The compounds are useful in the control of parasites. Certain of the compounds have antimicrobial properties.

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Reference£º
Copper catalysis in organic synthesis – NCBI,
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”