Graphdiyne(GDY)has attracted considerable attention as a new two-dimensional(2D)carbon hybrid material because of its good conductivity,adjustable electronic structure,and special electron transfer enhancement propert...Graphdiyne(GDY)has attracted considerable attention as a new two-dimensional(2D)carbon hybrid material because of its good conductivity,adjustable electronic structure,and special electron transfer enhancement properties.GDY has great potential in the field of photocatalytic water splitting for hydrogen evolution,owing to its unique properties.In this study,GDY was successfully prepared by the mechanochemical coupling of precursors C_(6)Br_(6) and CaC_(2) using a ball-milling approach.The prepared GDY,especially its microstructure and composition,was well characterized using different techniques such as X-ray diffraction,scanning electron microscopy,transmission electron microscopy,X-ray photoelectron spectroscopy(XPS),Fourier-transform infrared,and Raman characterization techniques.By exploiting the unique two-dimensional(2D)structure and outstanding light absorption properties of GDY,GDY/CdSe 2D/0D heterojunctions were successfully established and applied to photocatalytic hydrogen evolution.The hydrogen evolution activity of GDY/CdSe-20,a type of composite material,reached 6470μmol g^(-1) h^(-1),which is 461 and 40 times higher than that of GDY and CdSe,respectively.Moreover,the fine electrical conductivity of GDY enabled rapid and effective transfer of the photogenerated electrons in CdSe into the hydrogen evolution reaction.The transfer path of the photogenerated electrons was studied through XPS with in situ irradiation,and a reasonable mechanism for the hydrogen evolution reaction was proposed.This study provides a feasible approach for the large-scale preparation of GDY and demonstrates the prospects of GDY in the field of photocatalysis.展开更多
A straightforward protocol using readily available aromatic amines,N,N,N',N'-tetramethyl-p-phenylenediamine or N,N,N',N'-tetramethylbenzidine,as photocatalysts was developed for theefficient hydrodehal...A straightforward protocol using readily available aromatic amines,N,N,N',N'-tetramethyl-p-phenylenediamine or N,N,N',N'-tetramethylbenzidine,as photocatalysts was developed for theefficient hydrodehalogenation of organic halides,such as 4'-bromoacetophenone,polyfluoroarenes,cholorobenzene,and 2,2',4,4'-tetrabromodiphenyl ether(a resistant and persistent organic pollu-tant).The strongly reducing singlet excited states of the amines enabled diffusion-controlled disso-ciative electron transfer to effectively cleave carbon-halogen bonds,followed by radical hydrogena-tion.Diisopropylethylamine served as the terminal electron/proton donor and regenerated theamine sensitizers.展开更多
The IR spectroscopic data indicate the tautomeric transformations of typical aprotonic organic fluids such as methane halides with gross formulas CHX3 （X = Cl, Br）, CH2X2 （X = CI, Br, I） and CCl4 at normal conditi...The IR spectroscopic data indicate the tautomeric transformations of typical aprotonic organic fluids such as methane halides with gross formulas CHX3 （X = Cl, Br）, CH2X2 （X = CI, Br, I） and CCl4 at normal conditions. These transformations lead to the appearance in molecules of activated hydrogen atoms similar in the spectral behaviour to the bounded proton. The classical analysis of IR bands in 5000-600 cm^-1 region, for studied samples and their deuterated derivatives, proves the existence in the presented organic fluids of hydrogen and dihydrogen bonds. This bonding promotes the formation of supramolecular structure in methane halides. The mechanism of unusual binding in liquid phase in terms of common knowledge for the basic chemical properties of the examined compounds is discussed.展开更多
文摘Graphdiyne(GDY)has attracted considerable attention as a new two-dimensional(2D)carbon hybrid material because of its good conductivity,adjustable electronic structure,and special electron transfer enhancement properties.GDY has great potential in the field of photocatalytic water splitting for hydrogen evolution,owing to its unique properties.In this study,GDY was successfully prepared by the mechanochemical coupling of precursors C_(6)Br_(6) and CaC_(2) using a ball-milling approach.The prepared GDY,especially its microstructure and composition,was well characterized using different techniques such as X-ray diffraction,scanning electron microscopy,transmission electron microscopy,X-ray photoelectron spectroscopy(XPS),Fourier-transform infrared,and Raman characterization techniques.By exploiting the unique two-dimensional(2D)structure and outstanding light absorption properties of GDY,GDY/CdSe 2D/0D heterojunctions were successfully established and applied to photocatalytic hydrogen evolution.The hydrogen evolution activity of GDY/CdSe-20,a type of composite material,reached 6470μmol g^(-1) h^(-1),which is 461 and 40 times higher than that of GDY and CdSe,respectively.Moreover,the fine electrical conductivity of GDY enabled rapid and effective transfer of the photogenerated electrons in CdSe into the hydrogen evolution reaction.The transfer path of the photogenerated electrons was studied through XPS with in situ irradiation,and a reasonable mechanism for the hydrogen evolution reaction was proposed.This study provides a feasible approach for the large-scale preparation of GDY and demonstrates the prospects of GDY in the field of photocatalysis.
文摘A straightforward protocol using readily available aromatic amines,N,N,N',N'-tetramethyl-p-phenylenediamine or N,N,N',N'-tetramethylbenzidine,as photocatalysts was developed for theefficient hydrodehalogenation of organic halides,such as 4'-bromoacetophenone,polyfluoroarenes,cholorobenzene,and 2,2',4,4'-tetrabromodiphenyl ether(a resistant and persistent organic pollu-tant).The strongly reducing singlet excited states of the amines enabled diffusion-controlled disso-ciative electron transfer to effectively cleave carbon-halogen bonds,followed by radical hydrogena-tion.Diisopropylethylamine served as the terminal electron/proton donor and regenerated theamine sensitizers.
文摘The IR spectroscopic data indicate the tautomeric transformations of typical aprotonic organic fluids such as methane halides with gross formulas CHX3 （X = Cl, Br）, CH2X2 （X = CI, Br, I） and CCl4 at normal conditions. These transformations lead to the appearance in molecules of activated hydrogen atoms similar in the spectral behaviour to the bounded proton. The classical analysis of IR bands in 5000-600 cm^-1 region, for studied samples and their deuterated derivatives, proves the existence in the presented organic fluids of hydrogen and dihydrogen bonds. This bonding promotes the formation of supramolecular structure in methane halides. The mechanism of unusual binding in liquid phase in terms of common knowledge for the basic chemical properties of the examined compounds is discussed.
