Activated carbons were prepared by two chemical methods and the adsorption of Cu(II) on activated carbons from aqueous solution containing amino groups was studied. The first method involved the chlorination of activa...Activated carbons were prepared by two chemical methods and the adsorption of Cu(II) on activated carbons from aqueous solution containing amino groups was studied. The first method involved the chlorination of activated carbon following by substitution of chloride groups with amino groups, and the second involved the nitrilation of activated carbon with reduction of nitro groups to amino groups. Resultant activated carbons were characterized in terms of porous structure, elemental analysis, FTIR spectroscopy, XPS, Boehm titration,and p Hzpc. Kinetic and equilibrium tests were performed for copper adsorption in the batch mode. Also,adsorption mechanism and effect of p H on the adsorption of Cu(II) ions were discussed. Adsorption study shows enhanced adsorption for copper on the modified activated carbons, mainly by the presence of amino groups, and the Freundlich model is applicable for the activated carbons. It is suggested that binding of nitrogen atoms with Cu(II) ions is stronger than that with H+ions due to relatively higher divalent charge or stronger electrostatic force.展开更多
A series of novel wide bandgap small molecules(IFT-ECA, IFT-M, IFT-TH and IFT-IC) based on the A-D-A structure with indenofluorene core, thiophene bridge, and different electron-deficient end-capping groups, were synt...A series of novel wide bandgap small molecules(IFT-ECA, IFT-M, IFT-TH and IFT-IC) based on the A-D-A structure with indenofluorene core, thiophene bridge, and different electron-deficient end-capping groups, were synthesized and used as non-fullerene acceptors in organic solar cells. The influences of end-capping groups on the device performance were studied.The four materials exhibited different physical and chemical properties due to the variation of end-capping groups, which further affect the exciton dissociation, charge transport, morphology of the bulk-heterojunction films and device performance. Among them, IFT-IC-based device delivered the best power conversion efficiency of 7.16% due to proper nano-scale phase separation morphology and high electron mobility, while the devices based on the other acceptors achieved lower device performance(4.14% for IFT-TH, <1% for IFT-ECA and IFT-M). Our results indicate the importance of choosing suitable electron-withdrawing groups to construct high-performance non-fullerene acceptors based on A-D-A motif.展开更多
Oxygen reduction reactions(ORRs)with one-or two-electron-transfer pathways are the essential process for aprotic metal-oxygen batteries,in which the stability of superoxide intermediates/products(O_(2)^(-),LiO_(2),NaO...Oxygen reduction reactions(ORRs)with one-or two-electron-transfer pathways are the essential process for aprotic metal-oxygen batteries,in which the stability of superoxide intermediates/products(O_(2)^(-),LiO_(2),NaO_(2),etc.)mainly dominates the ORR activity/stability and battery performance.However,little success in regulating the stability of the superoxides has been achieved due to their highly reactive characteristics.Herein,we identified and modulated the stability of superoxides by introducing anthraquinone derivatives as cocatalysts which functioned as superoxide trapper adsorbing the superoxides generated via surface-mediated ORR and then transferring them from the solid catalyst surface into electrolyte.Among the studied trappers,1,4-difluoroanthraquinone(DFAQ)with electron-withdrawing groups showed the highest adsorption towards superoxides and could efficiently stabilize LiO_(2)in electrolyte,which greatly promoted the surface-mediated ORR rate and stability.This highlighted the magnitude of adsorption between the trapper and LiO_(2)on the ORR activity/stability.Using an aprotic Li-O_(2)battery as a model metal-O_(2)battery,the overall performance of the cell with DFAQ was substantially improved in terms of cell capacity,rate capability and cyclic stability.These results represent a significant advance in the understanding of ORR mechanisms and promoting the performance of metal-O_(2)batteries.展开更多
文摘Activated carbons were prepared by two chemical methods and the adsorption of Cu(II) on activated carbons from aqueous solution containing amino groups was studied. The first method involved the chlorination of activated carbon following by substitution of chloride groups with amino groups, and the second involved the nitrilation of activated carbon with reduction of nitro groups to amino groups. Resultant activated carbons were characterized in terms of porous structure, elemental analysis, FTIR spectroscopy, XPS, Boehm titration,and p Hzpc. Kinetic and equilibrium tests were performed for copper adsorption in the batch mode. Also,adsorption mechanism and effect of p H on the adsorption of Cu(II) ions were discussed. Adsorption study shows enhanced adsorption for copper on the modified activated carbons, mainly by the presence of amino groups, and the Freundlich model is applicable for the activated carbons. It is suggested that binding of nitrogen atoms with Cu(II) ions is stronger than that with H+ions due to relatively higher divalent charge or stronger electrostatic force.
基金supported by the Ministry of Science and Technology(2014CB643501)the National Natural Science Foundation of China(21520102006,21634004,21490573)the Guangdong Natural Science Foundation(S2012030006232)
文摘A series of novel wide bandgap small molecules(IFT-ECA, IFT-M, IFT-TH and IFT-IC) based on the A-D-A structure with indenofluorene core, thiophene bridge, and different electron-deficient end-capping groups, were synthesized and used as non-fullerene acceptors in organic solar cells. The influences of end-capping groups on the device performance were studied.The four materials exhibited different physical and chemical properties due to the variation of end-capping groups, which further affect the exciton dissociation, charge transport, morphology of the bulk-heterojunction films and device performance. Among them, IFT-IC-based device delivered the best power conversion efficiency of 7.16% due to proper nano-scale phase separation morphology and high electron mobility, while the devices based on the other acceptors achieved lower device performance(4.14% for IFT-TH, <1% for IFT-ECA and IFT-M). Our results indicate the importance of choosing suitable electron-withdrawing groups to construct high-performance non-fullerene acceptors based on A-D-A motif.
基金the National Natural Science Foundation of China(21773055,U1604122,51702086,21203055and 21805070)the Program for Science&Technology Innovation Talents in Universities of Henan Province(18HASTIT004)China Postdoctoral Science Foundation(2020M672201)。
文摘Oxygen reduction reactions(ORRs)with one-or two-electron-transfer pathways are the essential process for aprotic metal-oxygen batteries,in which the stability of superoxide intermediates/products(O_(2)^(-),LiO_(2),NaO_(2),etc.)mainly dominates the ORR activity/stability and battery performance.However,little success in regulating the stability of the superoxides has been achieved due to their highly reactive characteristics.Herein,we identified and modulated the stability of superoxides by introducing anthraquinone derivatives as cocatalysts which functioned as superoxide trapper adsorbing the superoxides generated via surface-mediated ORR and then transferring them from the solid catalyst surface into electrolyte.Among the studied trappers,1,4-difluoroanthraquinone(DFAQ)with electron-withdrawing groups showed the highest adsorption towards superoxides and could efficiently stabilize LiO_(2)in electrolyte,which greatly promoted the surface-mediated ORR rate and stability.This highlighted the magnitude of adsorption between the trapper and LiO_(2)on the ORR activity/stability.Using an aprotic Li-O_(2)battery as a model metal-O_(2)battery,the overall performance of the cell with DFAQ was substantially improved in terms of cell capacity,rate capability and cyclic stability.These results represent a significant advance in the understanding of ORR mechanisms and promoting the performance of metal-O_(2)batteries.
