Ju Mei,†,‡,∥ Nelson L. C. Leung,†,‡,∥ Ryan T. K. Kwok,†,‡ Jacky W. Y. Lam,†,‡ and Ben Zhong Tang*,†,‡,§ †HKUST-Shenzhen Research Institute, Hi-Tech Park, Nanshan, Shenzhen 518057, China ‡Department of Chemistry, HKUST Jockey Club Institute for Advanced Study, Institute of Molecular Functional Materials, Division of Biomedical Engineering, State Key Laboratory of Molecular Neuroscience, Division of Life Science, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China Guangdong Innovative Research Team, SCUT-HKUST Joint Research Laboratory, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China

Aggregation-Induced Emission: Together We Shine, United We Soar!

비만아 부모의 돌봄 경험: q 방법론

Rapidly increasing atmospheric CO2 concentrations threaten human society, the natural environment, and the synergy between the two. In order to ameliorate the CO2 problem, carbon capture and conversion techniques have been proposed. Metal–organic framework (MOF)-based materials, a relatively new class of porous materials with unique structural features, high surface areas, chemical tunability and stability, have been extensively studied with respect to their applicability to such techniques. Recently, it has become apparent that the CO2 capture capabilities of MOF-based materials significantly boost their potential toward CO2 conversion. Furthermore, MOF-based materials’ well-defined structures greatly facilitate the understanding of structure–property relationships and their roles in CO2 capture and conversion. In this review, we provide a comprehensive account of significant progress in the design and synthesis of MOF-based materials, including MOFs, MOF composites and MOF derivatives, and their application to carbon capture and conversion. Special emphases on the relationships between CO2 capture capacities of MOF-based materials and their catalytic CO2 conversion performances are discussed.

Carbon capture and conversion using metal–organic frameworks and MOF-based materials

Photoreduction of CO2 into sustainable and green solar fuels is generally believed to be an appealing solution to simultaneously overcome both environmental problems and energy crisis. The low selectivity of challenging multi-electron CO2 photoreduction reactions makes it one of the holy grails in heterogeneous photocatalysis. This Review highlights the important roles of cocatalysts in selective photocatalytic CO2 reduction into solar fuels using semiconductor catalysts. A special emphasis in this review is placed on the key role, design considerations and modification strategies of cocatalysts for CO2 photoreduction. Various cocatalysts, such as the biomimetic, metal-based, metal-free, and multifunctional ones, and their selectivity for CO2 photoreduction are summarized and discussed, along with the recent advances in this area. This Review provides useful information for the design of highly selective cocatalysts for photo(electro)reduction and electroreduction of CO2 and complements the existing reviews on various semiconductor photocatalysts.

Cocatalysts for Selective Photoreduction of CO2 into Solar Fuels.

Photocatalysts and Photoelectrodes James L. White,† Maor F. Baruch,† James E. Pander III,† Yuan Hu,† Ivy C. Fortmeyer,† James Eujin Park,† Tao Zhang,† Kuo Liao,† Jing Gu,‡ Yong Yan,‡ Travis W. Shaw,† Esta Abelev,† and Andrew B. Bocarsly*,† †Department of Chemistry, Princeton University, Princeton, New Jersey 08544, United States ‡Chemical and Materials Science Center, National Renewable Energy Laboratory, Golden, Colorado 80401, United States

Light-Driven Heterogeneous Reduction of Carbon Dioxide: Photocatalysts and Photoelectrodes

Organic-inorganic metal halide hybrids are an important class of crystalline materials with exceptional structural and property tunability. Recently metal halide perovskites with ABX3 structure have been extensively investigated as new generation semiconductors for various optoelectronic devices, including photovoltaic cells, light emitting diodes, photodetectors, and lasers, for their exceptional optical and electronic properties. By controlling the morphological dimensionality, low dimensional metal halide perovskites, including 2D perovskite nanoplatelets, 1D perovskite nanowires, and 0D perovskite quantum dots, have been developed to exhibit distinct properties from their bulk counterparts, due to quantum size effects. Besides ABX3 perovskites, organic-inorganic metal halide hybrids, containing the same fundamental building block of metal halide octahedra (BX6), can also be assembled to possess other types of crystallographic structures. Using appropriate organic and inorganic components, low dimensional organic-inorganic metal halide hybrids with 2D, quasi-2D, corrugated-2D, 1D, and 0D structures at the molecular level have been developed and studied. Due to the strong quantum confinement and site isolation, these low dimensional metal halide hybrids at the molecular level exhibit remarkable and unique properties that are significantly different from those of ABX3 perovskites. In light of the rapid development of low dimensional metal halide perovskites and hybrids, it is indeed timely to review the recent progress in these areas. Also, there is a need to clarify the difference between morphological low dimensional metal halide perovskites and molecular level low dimensional metal halide hybrids, as currently the terminologies of low dimensional perovskites are not appropriately used in many cases. In this review article, we discuss the synthesis, characterization, application, and computational studies of low dimensional metal halide perovskites and hybrids.

Low dimensional metal halide perovskites and hybrids

Scintillation based X-ray detection has received great attention for its application in a wide range of areas from security to healthcare. Here, we report highly efficient X-ray scintillators with state-of-the-art performance based on an organic metal halide, ethylenebis-triphenylphosphonium manganese (II) bromide ((C38H34P2)MnBr4), which can be prepared using a facile solution growth method at room temperature to form inch sized single crystals. This zero-dimensional organic metal halide hybrid exhibits green emission peaked at 517 nm with a photoluminescence quantum efficiency of ~ 95%. Its X-ray scintillation properties are characterized with an excellent linear response to X-ray dose rate, a high light yield of ~ 80,000 photon MeV−1, and a low detection limit of 72.8 nGy s−1. X-ray imaging tests show that scintillators based on (C38H34P2)MnBr4 powders provide an excellent visualization tool for X-ray radiography, and high resolution flexible scintillators can be fabricated by blending (C38H34P2)MnBr4 powders with polydimethylsiloxane. Scintillation-based X-ray detection is promising for applications in various areas ranging from security to healthcare, and low-cost and eco-friendly scintillation materials would be beneficial. Here the authors report a facile solution growth of organic manganese halide for efficient X-ray scintillation.

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Highly efficient eco-friendly X-ray scintillators based on an organic manganese halide.

Recent advances in lanthanide luminescence with metal-organic chromophores as sensitizers

Highly phosphorescent (Ph4 P)2 [MnBr4 ] as a low-cost and environmentally benign emitting material achieves peak current efficiency of 25.4 cd A-1 and external quantum efficiency (EQE) of 7.2% for nondoped organic light-emitting diodes, and peak current efficiency of 32.0 cd A-1 and EQE of 9.6% for doped devices with 20% (Ph4 P)2 [MnBr4 ]:27% TCTA:53% 6DCZPPY as a doping emitting layer.

Green-Light-Emitting Diodes based on Tetrabromide Manganese(II) Complex through Solution Process.

A promising coordination polymer photocatalyst (Y[Ir(ppy)2(dcbpy)]2[OH]) (Ir-CP, ppy = 2-phenylpyridine, dcbpy = 2,2′-bipyridine-4,4′-dicarboxylate) based on a highly efficient light-harvesting Ir unit, Ir(ppy)2(Hdcbpy), has been obtained, with good stability and exhibiting visible-light absorption over a broad range, arising from the metal-to-ligand charge transfer (3MLCT) and ligand-to-ligand charge transfer (LLCT). The designed Ir-CP heterogeneous photocatalyst acts as both a photosensitizer to harvest visible light, and an active catalyst for CO2 photoreduction. Due to the broad absorption in the UV-visible region and long-lived excited states of Ir-CP, the photocatalyst can efficiently catalyze CO2 reduction under visible-light irradiation in a heterogeneous photocatalytic system. For the first time, the remarkable photocatalytic efficiency of Ir-CP under visible-light irradiation (38 μmol HCOO− was produced in 6 h) was shown. Moreover, Ir-CP shows high photostability during CO2 photoreduction, which promotes the recyclability of the heterogeneous photocatalyst.

Liang-Jin Xu

Papers

Low dimensional metal halide perovskites and hybrids

Highly efficient eco-friendly X-ray scintillators based on an organic manganese halide.

Recent advances in lanthanide luminescence with metal-organic chromophores as sensitizers

Green-Light-Emitting Diodes based on Tetrabromide Manganese(II) Complex through Solution Process.

Effective visible-light driven CO2 photoreduction via a promising bifunctional iridium coordination polymer