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Carbon dioxide reduction together with aerobic oxidative cyclization using eosin Y-based light-harvesting photocatalysts remains a key challenge. In this study, we present the first-ever synthesis of unique in situ Se-infused eosin Y (Sein–EY) flexible photocatalysts through a simple one-pot method. The as-synthesized Sein–EY flexible film photocatalyst exhibits outstanding performance for the production of formic acid (204 μM in 2 h) and aerobic oxidative cyclization of thioamides via the formation of C–N/C–S bonds with outstanding yields (98.6%) when exposed to solar light. The presence of infused Se significantly extends the solar light absorption capacity of the Sein–EY photocatalyst, reaching up to 580 nm. This study opens up a new pathway for the rational design and synthesis of potentially effective Se-infused-EY photocatalysts through a simple and scalable method, enabling both solar chemical production and efficient one-pot three-component reactions. [ABSTRACT FROM AUTHOR]

Topological insulators, a class of materials possessing bulk bandgap and metallic surface states with a topological nontrivial symmetry, are considered promising candidates for emerging quantum and optoelectronic applications. However, achieving scalable growth and control over the parameters including thickness, carrier density, bulk bandgap, and defect density remains a challenge in realizing such applications. In this work, we show the scalable growth of topological insulator alloys Bi2Se(3−x)Sx and demonstrate composition-tunable bandgap, using chemical vapor deposition (CVD). A bandgap increase of up to ∼40% at a sulfur concentration of ∼15% is demonstrated. Correspondingly, the real part (n) of the refractive index is reduced in the alloy by ∼25% relative to that of Bi2Se3. Additionally, electronic transport measurements indicate a bulk p-type doping and field-effect tunable metallic surface states of the alloy. This work paves the way for the controlled growth of topological insulators, free from surface-state pinning, suitable for quantum optoelectronics and spintronics applications. [ABSTRACT FROM AUTHOR]

Two-dimensional covalent organic frameworks (2D COFs) are a class of crystalline polymers with a design controllable platform that may be developed into a new type of metal-free photocatalyst. The exploration of new frameworks is, however, critical for further progress in this emerging field. To realize their full potential in practical light harvesting applications, the fabrication of a film type photocatalyst is equally essential. Here, we report the successful development of a triazine based covalent organic framework (2D CTF) as an inexpensive and highly efficient visible light active flexible film photocatalyst for solar fuel production from CO2. For this research work, the condensation polymerization between cyanuric chloride and perylene diimide has been exploited for the first time as a new synthetic approach to the construction of 2D CTFs. The visible light-harvesting capacity, suitable band gap and highly ordered π electron channels contribute to the excellent performance of the film photocatalyst. The current study is a benchmark example of COF based photocatalysts for solar fuel production from CO2 and is expected to trigger further interest in potential solar energy conversion applications such as wearable devices. [ABSTRACT FROM AUTHOR]

The judicious utilization of solar light for the asymmetric synthesis of optically active compounds by imitating natural photosynthesis introduces a new concept that harnesses this renewable energy in vitro for ultimate transformation into chiral chemical bonds. Herein, we present a comprehensive description of such a biomimetic endeavor towards the design and construction of an asymmetric artificial photosynthesis system that comprises an efficient method of nicotinamide cofactor (NADPH) regeneration under visible light employing a graphene-based light harvesting photocatalyst and its subsequent utilization in an enzyme-catalyzed asymmetric reduction of prochiral ketones to expediently furnish the corresponding chiral secondary alcohols. A detailed optimization study revealed a major dependency of the reaction outcome on the amount of cofactor, photocatalyst and enzyme used, as well as the mode of their addition. A series of structurally diverse ketones bearing an array of (hetero)aryl/alkyl substituents proved to be highly suitable to our photocatalytic-biocatalytic cascade approach, providing (R/S)-1-(hetero)aryl/ alkylethanols in excellent enantioselectivities (ee ˜ 95->99.9%) under mild and environmentally benign conditions. To the best of our knowledge, the synthesis of these enantiopure alcohols employing a visible-light-driven nicotinamide cofactor regeneration strategy has been reported for the first time. Such enantioenriched alcohols act as versatile chiral building blocks for the synthesis of compounds having industrial and pharmaceutical relevance. In addition, this solar-to-chiral chemicals prototype appears advantageous from ecological and economical perspectives. We describe mechanistic pathways to demonstrate how the present catalytic synthesis protocol functions through perfect orchestration between visible-light-driven photocatalysis and biocatalysis to be successively applied in inducing asymmetry in an achiral molecule for the ultimate goal of solar energy utilization in the synthesis of valuable chiral fine chemicals. This work highlights the potential advantages of a bioinspired system to the pertinence of solar energy in asymmetric transformations leading to enantioenriched alcohol precursors, and thus opens up a new field of research that might emerge as an important breakthrough with promising implications towards generating a sustainable and non-fossil/non-nuclear energy future. [ABSTRACT FROM AUTHOR]

The utilization of CO2 for production of solar fuels/chemicals is gaining increasing importance due to worldwide fossil-fuel shortage and global warming. As a means to achieve this, we herein report on the synthesis and development of a graphene-based visible light active photocatalyst (CCG-BODIPY) which is chemically converted graphene (CCG) covalently bonded to a light harvesting BODIPY molecule (1-picolylamine-2-aminophenyl-3-oxy-phenyl-4,4'-difluoro -1,3,5,7-tetramethyl-2,6-diethyl-4-bora-3a,4a-diaza-s -indacene-triazine). The photocatalyst-biocatalyst coupled system developed using CCG-BODIPY as photocatalyst functions in a highly efficient manner, leading to high NADH regeneration (54.02 ± 0.61%), followed by its consumption in exclusive formic acid production (144.2 ± 1.8 µmol) from CO2. The present research endeavour highlights the development and application of a graphene based photocatalyst for direct solar fuel formation from carbon dioxide. [ABSTRACT FROM AUTHOR]