.In the past decade,lead halide perovskites have emerged as potential optoelectronic materials in the fields of light-emitting diode,solar cell,photodetector,and laser,due to their low-cost synthesis method,tunable ba....In the past decade,lead halide perovskites have emerged as potential optoelectronic materials in the fields of light-emitting diode,solar cell,photodetector,and laser,due to their low-cost synthesis method,tunable bandgap,high quantum yield,large absorption,gain coefficient,and low trap-state densities.In this review,we present a comprehensive discussion of lead halide perovskite applications,with an emphasis on recent advances in synthetic strategies,morphology control,and lasing performance.In particular,the synthetic strategies of solution and vapor progress and the morphology control of perovskite nanocrystals are reviewed.Furthermore,we systematically discuss the latest development of perovskite laser with various fundamental performances,which are highly dependent on the dimension and size of nanocrystals.Finally,considering current challenges and perspectives on the development of lead halide perovskite nanocrystals,we provide an outlook on achieving high-quality lead perovskite lasers and expanding their practical applications.展开更多
NaTi_2 (PO_4)_3 (NTP) nanocrystals with high room-temperature ionic conductivity of 1.1×10~3 S/cm were prepared by a concise solvothermal method at 140 ℃ for 3 h, and the aspect ratios of all the NTP nanocrystal...NaTi_2 (PO_4)_3 (NTP) nanocrystals with high room-temperature ionic conductivity of 1.1×10~3 S/cm were prepared by a concise solvothermal method at 140 ℃ for 3 h, and the aspect ratios of all the NTP nanocrystals are the closest to 0.7. It implies a moderate size-distribution of NTP nanocrystals obtained at 140 ℃ for 3 h is helpful for increasing packing density, and the packing density is the larger, so its conductivity is the higher. The controllability over size and morphology of the NTP nanocrystals via solvothermal temperature and time were investigated. The results suggest that our method is of great potential in synthesizing NTP nanocrystals with high room-temperature ionic conductivity at low cost.展开更多
In wet chemical syntheses of noble metal nanocrystals,surfactants play crucial roles in regulating their morphology.To date,more attention has been paid to the effect of the surfactant on the surface energy of crystal...In wet chemical syntheses of noble metal nanocrystals,surfactants play crucial roles in regulating their morphology.To date,more attention has been paid to the effect of the surfactant on the surface energy of crystal facets,while less attention has been paid to its effect on the growth kinetics.In this paper,using the growth of Au-Pd alloy nanocrystals as an example,we demonstrate that different concentration of surfactant hexadecyltrimethyl ammonium chloride(CTAC)may cause the different packing density of CTA+bilayers on different sites(face,edge or vertex)of crystallite surface,which would change the crystal growth kinetics and result in preferential crystal growth along the edge or vertex of crystallites.The unique shape evolution from trisoctahedron to excavated rhombic dodecahedron and multipod structure for Au-Pd alloy nanocrystals was successfully achieved by simply adjusting the concentration of CTAC.These results help to understand the effect of surfactants on the shape evolution of nanocrystals and open up avenues to the rational synthesis of nanocrystals with the thermodynamically unfavorable morphologies.展开更多
Cu2O nanocubes,octahedra,spheres and truncated rhombic dodecahedral were prepared and their structural,morphological,and electronic properties were investigated by X-ray diffraction analysis.X-ray absorption near edge...Cu2O nanocubes,octahedra,spheres and truncated rhombic dodecahedral were prepared and their structural,morphological,and electronic properties were investigated by X-ray diffraction analysis.X-ray absorption near edge structure,scanning electron microscope and transmission electron microscope and X-ray absorption near edge structure.Cu2O nanocrystals were successfully employed to catalyze the 1,3-dipolar cycloaddition reaction for the synthesis of 1,4-disubstituted triazoles.Cu2O nanocubes and octahedral showed the superior catalytic performance in the cycloaddition reaction.These results reveal that crystal-plane engineering of oxide catalysts is a useful strategy for developing efficient catalysts for organic reaction.展开更多
Elucidation of the CuOx-CeO2 interactions is of great interest and importance in understanding complex CuOx-CeO2 interfacial catalysis in various reactions. In the present work, we have investigated structures and cat...Elucidation of the CuOx-CeO2 interactions is of great interest and importance in understanding complex CuOx-CeO2 interfacial catalysis in various reactions. In the present work, we have investigated structures and catalytic activity in CO oxidation of CuOx species on CeO2 rods, cubes and polyhedra predominantly exposing {110}+{100}, {100} and {111} facets by the incipient wetness impregnation method with the lowest Cu loading of 0.025%. The structural evolution of CuOx species was found to depend on both the Cu loading and the CeO2 morphology. As the Cu loading increases, CuOx species are deposited preferentially on the surface defect of CeO2 and then aggregate and grow, accompanied by the formation of isolated Cu ions, CuOx clusters strongly/weakly interacting with the CeO2, highly dispersed Cu O nanoparticles, and large Cu O nanoparticles. The isolated Cu^+ species and CuOx clusters weakly interacting with the CeO2 were observed mainly on the O-terminated CeO2{100} facets. Meanwhile, more Cu(I) species are stabilized during CO reduction processes in CuOx/c-CeO2 catalysts than in CuOx/r-CeO2 and CuOx/p-CeO2 catalysts. The catalytic activities of various CuOx/CeO2 catalysts in CO oxidation vary with both the CuOx species and the CeO2 morphology. These results comprehensively elucidate the CuOx-CeO2 interactions and exemplify their morphology-dependence.展开更多
基金This work was supported by the National Key R&D Program of China(2018YFB2200500,2017YFE0123700)the National Natural Science Foundation of China(61975023,61875211,22072010,61925507,61905264,62005296,and 92050203)+5 种基金the Strategic Priority Research Program of CAS(XDB16030400)CAS Interdisciplinary Innovation Team,Program of Shanghai Academic/Technology Research Leader(Grant No.18XD1404200)China Postdoctoral Science Foundation(2020M681421)Chongqing Research Program of Basic Research and Frontier Technology(cstc2018jszxcyzdX0137)the Natural Science Foundation of Chongqing(cstc2019jcyj-msxmX0522)the Science and Technology Research Program of Chongqing Municipal Education Commission(KJQN201900515).
文摘.In the past decade,lead halide perovskites have emerged as potential optoelectronic materials in the fields of light-emitting diode,solar cell,photodetector,and laser,due to their low-cost synthesis method,tunable bandgap,high quantum yield,large absorption,gain coefficient,and low trap-state densities.In this review,we present a comprehensive discussion of lead halide perovskite applications,with an emphasis on recent advances in synthetic strategies,morphology control,and lasing performance.In particular,the synthetic strategies of solution and vapor progress and the morphology control of perovskite nanocrystals are reviewed.Furthermore,we systematically discuss the latest development of perovskite laser with various fundamental performances,which are highly dependent on the dimension and size of nanocrystals.Finally,considering current challenges and perspectives on the development of lead halide perovskite nanocrystals,we provide an outlook on achieving high-quality lead perovskite lasers and expanding their practical applications.
基金financially supported by the National Natural Science Foundation of China(Nos. 2016YFF0100901, 61274054 and 61504064)
文摘NaTi_2 (PO_4)_3 (NTP) nanocrystals with high room-temperature ionic conductivity of 1.1×10~3 S/cm were prepared by a concise solvothermal method at 140 ℃ for 3 h, and the aspect ratios of all the NTP nanocrystals are the closest to 0.7. It implies a moderate size-distribution of NTP nanocrystals obtained at 140 ℃ for 3 h is helpful for increasing packing density, and the packing density is the larger, so its conductivity is the higher. The controllability over size and morphology of the NTP nanocrystals via solvothermal temperature and time were investigated. The results suggest that our method is of great potential in synthesizing NTP nanocrystals with high room-temperature ionic conductivity at low cost.
基金supported by the National Basic Research Program of China (2015CB932301)the National Key Research and Development Program of China (2017YFA0206801)the National Natural Science Foundation of China (21333008, 21773190 and J1310024)
文摘In wet chemical syntheses of noble metal nanocrystals,surfactants play crucial roles in regulating their morphology.To date,more attention has been paid to the effect of the surfactant on the surface energy of crystal facets,while less attention has been paid to its effect on the growth kinetics.In this paper,using the growth of Au-Pd alloy nanocrystals as an example,we demonstrate that different concentration of surfactant hexadecyltrimethyl ammonium chloride(CTAC)may cause the different packing density of CTA+bilayers on different sites(face,edge or vertex)of crystallite surface,which would change the crystal growth kinetics and result in preferential crystal growth along the edge or vertex of crystallites.The unique shape evolution from trisoctahedron to excavated rhombic dodecahedron and multipod structure for Au-Pd alloy nanocrystals was successfully achieved by simply adjusting the concentration of CTAC.These results help to understand the effect of surfactants on the shape evolution of nanocrystals and open up avenues to the rational synthesis of nanocrystals with the thermodynamically unfavorable morphologies.
基金the Iranian National Science Foundation(INSF)Sharif University of Technology and University of Maragheh for financial supports of this work
文摘Cu2O nanocubes,octahedra,spheres and truncated rhombic dodecahedral were prepared and their structural,morphological,and electronic properties were investigated by X-ray diffraction analysis.X-ray absorption near edge structure,scanning electron microscope and transmission electron microscope and X-ray absorption near edge structure.Cu2O nanocrystals were successfully employed to catalyze the 1,3-dipolar cycloaddition reaction for the synthesis of 1,4-disubstituted triazoles.Cu2O nanocubes and octahedral showed the superior catalytic performance in the cycloaddition reaction.These results reveal that crystal-plane engineering of oxide catalysts is a useful strategy for developing efficient catalysts for organic reaction.
文摘Elucidation of the CuOx-CeO2 interactions is of great interest and importance in understanding complex CuOx-CeO2 interfacial catalysis in various reactions. In the present work, we have investigated structures and catalytic activity in CO oxidation of CuOx species on CeO2 rods, cubes and polyhedra predominantly exposing {110}+{100}, {100} and {111} facets by the incipient wetness impregnation method with the lowest Cu loading of 0.025%. The structural evolution of CuOx species was found to depend on both the Cu loading and the CeO2 morphology. As the Cu loading increases, CuOx species are deposited preferentially on the surface defect of CeO2 and then aggregate and grow, accompanied by the formation of isolated Cu ions, CuOx clusters strongly/weakly interacting with the CeO2, highly dispersed Cu O nanoparticles, and large Cu O nanoparticles. The isolated Cu^+ species and CuOx clusters weakly interacting with the CeO2 were observed mainly on the O-terminated CeO2{100} facets. Meanwhile, more Cu(I) species are stabilized during CO reduction processes in CuOx/c-CeO2 catalysts than in CuOx/r-CeO2 and CuOx/p-CeO2 catalysts. The catalytic activities of various CuOx/CeO2 catalysts in CO oxidation vary with both the CuOx species and the CeO2 morphology. These results comprehensively elucidate the CuOx-CeO2 interactions and exemplify their morphology-dependence.
