A new method of synthesizing single-component molecular conductor [Ni(dmit)2] by the reaction 2(Me4N)[Ni(dmit)2]2 [Ni(dmit)2] + (Me4N)[Ni(dmit)2] is reported. [Ni(dmit)2] exhibits a semiconductive behavior above 167...A new method of synthesizing single-component molecular conductor [Ni(dmit)2] by the reaction 2(Me4N)[Ni(dmit)2]2 [Ni(dmit)2] + (Me4N)[Ni(dmit)2] is reported. [Ni(dmit)2] exhibits a semiconductive behavior above 167 K, while from 167 K down to the measuring limit of 60 K, it exhibits metallic conductivity.展开更多
In this work,semirigid linkers of the alkyl-thiophene-alkyl structure are developed to construct double-cable polymers.Three alkyl units,propyl(C3H6),hexyl(C6H12),and dodecyl(C12H24),are applied as semirigid linkers,y...In this work,semirigid linkers of the alkyl-thiophene-alkyl structure are developed to construct double-cable polymers.Three alkyl units,propyl(C3H6),hexyl(C6H12),and dodecyl(C12H24),are applied as semirigid linkers,yielding three double-cable polymers:PBC6-T,PBC12-T,and PBC24-T,respectively.PBC12-T which uses C6H12-thiophene-C6H12 linkers is found to exhibit the best device efficiency of 5.56%,while PBC6-T and PBC24-T with shorter or longer linkers yield device efficiencies of only 2.65%and 1.09%in single-component organic solar cells(SCOSCs).Further studies reveal that PBC12-T exhibits higher crystallinity and improved charge transport,resulting in better efficiencies.Our work provides an approach to construct double-cable conjugated polymers with long alkyl linkers,and it shows the importance of the linker length for the photovoltaic performance of SCOSCs.展开更多
The photovoltaic properties of double-cable conjugated polymers are significantly influenced by the length of the alkyl linkers that connect donor backbones and acceptor side units. In this study, a series of 2-(3-oxo...The photovoltaic properties of double-cable conjugated polymers are significantly influenced by the length of the alkyl linkers that connect donor backbones and acceptor side units. In this study, a series of 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile(IC)-based double-cable polymers with alkyl linkers ranging from C_8H_(16)to C_(16)H_(32)(Px, x = 8, 10, 12, 14, 16) were synthesized for single-component organic solar cells(SCOSCs). Among these, the linker length x = 12(P12) is found to optimize the power conversion efficiencies(PCEs) in SCOSCs. Specifically, PCEs increase from P8 to P12 and then decline from P12to P16. Detailed investigations of optical absorption, charge transport, and morphology provide insights into the underlying factors contributing to these PCE variations. The findings indicate that the exceptional photovoltaic properties observed in P12 can be attributed to three key factors: A delicate balance between enhanced charge separation facilitated by the increased spacer length and reduced crystallinity resulting from longer spacers, higher charge mobilities, and well-balanced hole/electron transport characteristics. This study highlights the critical role of linker length in determining the photovoltaic properties of double-cable conjugated polymer-based SCOSCs and offers valuable guidance for the design of novel double-cable conjugated polymers.展开更多
The molecular orientations of conjugated materials on the substrate mainly include edge-on,face-on,and end-on.Edge-on and face-on orientations have been widely observed,while end-on orientation has been rarely reporte...The molecular orientations of conjugated materials on the substrate mainly include edge-on,face-on,and end-on.Edge-on and face-on orientations have been widely observed,while end-on orientation has been rarely reported.Since in organic solar cells(OSCs)charge transport is along the vertical direction,end-on orientation with conjugated backbones perpendicular to the substrate is recognized as the ideal microstructure for OSCs.In this work,we for the first time obtained the preferential end-on orientation in a conjugated molecular dyad that contains a conjugated backbone as donor and perylene bisimide side units as acceptor.This was realized by introducing a fused-ring structure to replace linear terthiophenes with conjugated backbones,yielding F-MDPBI and L-MDPBI respectively.Surprisingly,a shifting trend of the molecular orientation from dominating edge-on in L-MDPBI to preferential end-on in F-MDPBI was observed.As a consequence,vertical charge carrier mobilities in F-MDPBI are one order of magnitude higher than those with preferential edge-on orientation,so single-component OSCs based on this molecular dyad as a single photoactive layer provided a power conversion efficiency of 4.89% compared to 1.70% based on L-MDPBI with preferential edge-on orientation.展开更多
Herein,a novel dual-emission fluorescence sensor array of carbonized polymer dots(CPDs)-Cu^(2+)has been proposed,in which CPDs were prepared by one-pot hydrothermal method and Cu^(2+)acting as a quencher was combined ...Herein,a novel dual-emission fluorescence sensor array of carbonized polymer dots(CPDs)-Cu^(2+)has been proposed,in which CPDs were prepared by one-pot hydrothermal method and Cu^(2+)acting as a quencher was combined with CPDs by electrostatic interaction.Four negatively charged glycosaminoglycans(GAGs)bearing different hydrophilic groups showed variable binding affinities towards CPDs-Cu^(2+).Upon reacting with these GAGs,the different fluorescence response signals of CPDs-Cu^(2+)can be further differentiated by principal component analysis(PCA).The CPDs-Cu^(2+)sensor array,not only allows the identification of four similarly structured GAGs,but also realizes the discrimination of different concentrations of the same GAGs and their mixtures.Remarkably,the identification of GAGs in biological fluids can also be achieved using our proposed single-component sensor array,validating its application potential.This new strategy avoids multiple sensing probes,broadens the application of tongue-mimic sensor arrays and provides a viable idea for the development of single component sensing platforms.展开更多
The recently emerged double-cable conjugated polymers have come into focus due to their significantly improved power conversion efficiencies (PCEs) in single-component organic solar cells (SCOSCs). In this work, the e...The recently emerged double-cable conjugated polymers have come into focus due to their significantly improved power conversion efficiencies (PCEs) in single-component organic solar cells (SCOSCs). In this work, the effect of chlorination in double-cable conjugated polymers with linear benzodithiophene backbone and pendant perylene bisimide on the photovoltaic performance in SCOSCs has been studied. After introducing chlorine atoms into conjugated side chains, the highest occupied molecular orbital level of the conjugated polymers is down-shifted, thus resulting in a higher open-circuit voltage. As a result, the chlorinated double-cable conjugated polymer exhibits improved photovoltaic performance from 3.46% to 3.57%.展开更多
The reserves of the Duobaoshan porphyry Cu-Au-Mo-Ag deposit(also referred to as the Duobaoshan porphyry Cu deposit)ranks first among the copper deposits in China and 33rd among the porphyry copper deposits in the worl...The reserves of the Duobaoshan porphyry Cu-Au-Mo-Ag deposit(also referred to as the Duobaoshan porphyry Cu deposit)ranks first among the copper deposits in China and 33rd among the porphyry copper deposits in the world.It has proven resources of copper(Cu),molybdenum(Mo),gold(Au),and silver(Ag)of 2.28×10^(6)t,80×10^(3)t,73 t,and 1046 t,respectively.The major characteristics of the Duobaoshan porphyry Cu deposit are as follows.It is located in a zone sandwiched by the Siberian,North China,and paleo-Pacific plates in an island arc tectonic setting and was formed by the Paleozoic mineralization and the Mesozoic mineralization induced by superposition and transformation.The metallogenic porphyries are the Middle Hercynian granodiorite porphyries.The alterations of surrounding rocks are distributed in a ring form.With silicified porphyries at the center,the alteration zones of K-feldspar,biotite,sericite,and propylite occur from inside to outside.This deposit is composed of 215 ore bodies(including 14 major ore bodies)in four mineralized zones.Ore body No.X in the No.3 mineralized zone has the largest resource reserves,accounting for more than 78%of the total reserves of the deposit.Major ore components include Cu,Mo,Au,Ag,Se,and Ga,which have an average content of 0.46%,0.015%,0.16 g/t,1.22 g/t,0.0003%,and 0.001%-0.003%,respectively.The ore minerals of this deposit primarily include pyrite,chalcopyrite,bornite,and molybdenite,followed by magnetite,hematite,rutile,gelenite,and sphalerite.The ore-forming fluids of this deposit were magmatic water in the early metallogenic stage and then the mixture of meteoric water and magmatic water at the late metallogenic stage.The ore-forming fluids experienced three stages.The ore-forming fluids of stageⅠhad a hydrochemical type of H_(2)O-CO_(2)-Na Cl,an ore-forming temperature of 375-650℃,and ore-forming pressure of 110-160 MPa.The ore-forming fluids of stageⅡhad a hydrochemical type of H_(2)O-CO_(2)-Na Cl,an ore-forming temperature of 310-350℃,and ore-forming pressure of 58-80 MPa.The ore-forming fluids of stageⅢhad a hydrochemical type of Na Cl-H_(2)O,an ore-forming temperature of 210-290℃,and ore-forming pressure of 5-12 MPa.The CuAu-Mo-Ag mineralization mainly occurred at stagesⅠandⅡ,with the ore-forming materials having a mixed crust-mantle source.The Duobaoshan porphyry Cu deposit was formed in the initial subduction environment of the Paleo-Asian Ocean Plate during the Early Ordovician.Then,due to the closure of the Mongol-Okhotsk Ocean and the subduction and compression of the Paleo-Pacific Ocean,a composite orogenic metallogenic model of the deposit was formed.In other words,it is a porphyry-epithermal copper-gold polymetallic mineralization system of composite orogeny consisting of Paleozoic island arcs and Mesozoic orogeny and extension.展开更多
基金supported by the National Natural Science Foundation of China(No.20172034)Foundation for Univemity Key Teacher by Ministry of Educationthe grant for the State Key Program of China.
文摘A new method of synthesizing single-component molecular conductor [Ni(dmit)2] by the reaction 2(Me4N)[Ni(dmit)2]2 [Ni(dmit)2] + (Me4N)[Ni(dmit)2] is reported. [Ni(dmit)2] exhibits a semiconductive behavior above 167 K, while from 167 K down to the measuring limit of 60 K, it exhibits metallic conductivity.
基金the Beijing Natural Science Foundation(No.JQ21006)the Ministry of Science and Technology(No.2018YFA0208504)+3 种基金the National Natural Science Foundation(Nos.92163128,52073016,21905018)of Chinathe Fundamental Research Funds for the Central Universities(Nos.buctrc201828,XK1802-2)Open Project of State Key Laboratory of Organic-Inorganic Composites(No.oic-202201006)Open Project of State Key Laboratory of Supramolecular Structure and Materials(No.sklssm202209).
文摘In this work,semirigid linkers of the alkyl-thiophene-alkyl structure are developed to construct double-cable polymers.Three alkyl units,propyl(C3H6),hexyl(C6H12),and dodecyl(C12H24),are applied as semirigid linkers,yielding three double-cable polymers:PBC6-T,PBC12-T,and PBC24-T,respectively.PBC12-T which uses C6H12-thiophene-C6H12 linkers is found to exhibit the best device efficiency of 5.56%,while PBC6-T and PBC24-T with shorter or longer linkers yield device efficiencies of only 2.65%and 1.09%in single-component organic solar cells(SCOSCs).Further studies reveal that PBC12-T exhibits higher crystallinity and improved charge transport,resulting in better efficiencies.Our work provides an approach to construct double-cable conjugated polymers with long alkyl linkers,and it shows the importance of the linker length for the photovoltaic performance of SCOSCs.
基金jointly supported by the Beijing Natural Science Foundation (Nos.2212045 and JQ21006)the National Natural Science Foundation of China (Nos.21905158, 52073016 and 92163128)+2 种基金further supported by the Fundamental Research Funds for the Central Universities (Nos.buctrc202111, buctrc201828, and XK1802-2)the Opening Foundation of State Key Laboratory of Organic-Inorganic Composites of Beijing University of Chemical Technology (No.oic-202201006)Jiangxi Provincial Department of Science and Technology (Nos.20202ACBL213004, 20212BCJ23035, jxsq2019102004)。
文摘The photovoltaic properties of double-cable conjugated polymers are significantly influenced by the length of the alkyl linkers that connect donor backbones and acceptor side units. In this study, a series of 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile(IC)-based double-cable polymers with alkyl linkers ranging from C_8H_(16)to C_(16)H_(32)(Px, x = 8, 10, 12, 14, 16) were synthesized for single-component organic solar cells(SCOSCs). Among these, the linker length x = 12(P12) is found to optimize the power conversion efficiencies(PCEs) in SCOSCs. Specifically, PCEs increase from P8 to P12 and then decline from P12to P16. Detailed investigations of optical absorption, charge transport, and morphology provide insights into the underlying factors contributing to these PCE variations. The findings indicate that the exceptional photovoltaic properties observed in P12 can be attributed to three key factors: A delicate balance between enhanced charge separation facilitated by the increased spacer length and reduced crystallinity resulting from longer spacers, higher charge mobilities, and well-balanced hole/electron transport characteristics. This study highlights the critical role of linker length in determining the photovoltaic properties of double-cable conjugated polymer-based SCOSCs and offers valuable guidance for the design of novel double-cable conjugated polymers.
基金Beijing Natural Science Foundation,Grant/Award Number:JQ210065NSFC,Grant/Award Numbers:52073016,92163128+4 种基金Fundamental Research Funds for the Central Universities,Grant/Award Numbers:buctrc201828,XK1802-2The opening Foundation of State Key Laboratory of Organic-Inorganic Composites,Beijing University of Chemical Technology,Grant/Award Number:oic-202201006Jiangxi Provincial Department of Science and Technology,Grant/Award Numbers:20202ACBL213004,20212BCJ23035,jxsq2019102004,20203BBE53062Jiangxi Academy of Sciences,Grant/Award Numbers:2021YSBG22034,2021YSBG22033,2020-YZD-3Australian Research Council,Grant/Award Number:FT180100594。
文摘The molecular orientations of conjugated materials on the substrate mainly include edge-on,face-on,and end-on.Edge-on and face-on orientations have been widely observed,while end-on orientation has been rarely reported.Since in organic solar cells(OSCs)charge transport is along the vertical direction,end-on orientation with conjugated backbones perpendicular to the substrate is recognized as the ideal microstructure for OSCs.In this work,we for the first time obtained the preferential end-on orientation in a conjugated molecular dyad that contains a conjugated backbone as donor and perylene bisimide side units as acceptor.This was realized by introducing a fused-ring structure to replace linear terthiophenes with conjugated backbones,yielding F-MDPBI and L-MDPBI respectively.Surprisingly,a shifting trend of the molecular orientation from dominating edge-on in L-MDPBI to preferential end-on in F-MDPBI was observed.As a consequence,vertical charge carrier mobilities in F-MDPBI are one order of magnitude higher than those with preferential edge-on orientation,so single-component OSCs based on this molecular dyad as a single photoactive layer provided a power conversion efficiency of 4.89% compared to 1.70% based on L-MDPBI with preferential edge-on orientation.
基金supported by the National Natural Science Foundation of China(22274053)the Fundamental Research Funds for the Central Universities
文摘Herein,a novel dual-emission fluorescence sensor array of carbonized polymer dots(CPDs)-Cu^(2+)has been proposed,in which CPDs were prepared by one-pot hydrothermal method and Cu^(2+)acting as a quencher was combined with CPDs by electrostatic interaction.Four negatively charged glycosaminoglycans(GAGs)bearing different hydrophilic groups showed variable binding affinities towards CPDs-Cu^(2+).Upon reacting with these GAGs,the different fluorescence response signals of CPDs-Cu^(2+)can be further differentiated by principal component analysis(PCA).The CPDs-Cu^(2+)sensor array,not only allows the identification of four similarly structured GAGs,but also realizes the discrimination of different concentrations of the same GAGs and their mixtures.Remarkably,the identification of GAGs in biological fluids can also be achieved using our proposed single-component sensor array,validating its application potential.This new strategy avoids multiple sensing probes,broadens the application of tongue-mimic sensor arrays and provides a viable idea for the development of single component sensing platforms.
基金the National Natural Science Foundation of China(Nos.51973169,51703172 and 52073016)the Open Project Program of Wuhan National Laboratory for Optoelectronics(No.2020WNLOKF015)the science foundation of Wuhan Institute of Technology(No.K202025).
文摘The recently emerged double-cable conjugated polymers have come into focus due to their significantly improved power conversion efficiencies (PCEs) in single-component organic solar cells (SCOSCs). In this work, the effect of chlorination in double-cable conjugated polymers with linear benzodithiophene backbone and pendant perylene bisimide on the photovoltaic performance in SCOSCs has been studied. After introducing chlorine atoms into conjugated side chains, the highest occupied molecular orbital level of the conjugated polymers is down-shifted, thus resulting in a higher open-circuit voltage. As a result, the chlorinated double-cable conjugated polymer exhibits improved photovoltaic performance from 3.46% to 3.57%.
基金funded by the National Scientific and Technological Basic Resources Investigation Program(2022FY101800)a project of the National Natural Science Foundation of China(42102087)+1 种基金a project of the China Postdoctoral Science Foundation(2022M712966)a major project of the Ministry of Science and Technology of the People’s Republic of China(2021QZKK0304)。
文摘The reserves of the Duobaoshan porphyry Cu-Au-Mo-Ag deposit(also referred to as the Duobaoshan porphyry Cu deposit)ranks first among the copper deposits in China and 33rd among the porphyry copper deposits in the world.It has proven resources of copper(Cu),molybdenum(Mo),gold(Au),and silver(Ag)of 2.28×10^(6)t,80×10^(3)t,73 t,and 1046 t,respectively.The major characteristics of the Duobaoshan porphyry Cu deposit are as follows.It is located in a zone sandwiched by the Siberian,North China,and paleo-Pacific plates in an island arc tectonic setting and was formed by the Paleozoic mineralization and the Mesozoic mineralization induced by superposition and transformation.The metallogenic porphyries are the Middle Hercynian granodiorite porphyries.The alterations of surrounding rocks are distributed in a ring form.With silicified porphyries at the center,the alteration zones of K-feldspar,biotite,sericite,and propylite occur from inside to outside.This deposit is composed of 215 ore bodies(including 14 major ore bodies)in four mineralized zones.Ore body No.X in the No.3 mineralized zone has the largest resource reserves,accounting for more than 78%of the total reserves of the deposit.Major ore components include Cu,Mo,Au,Ag,Se,and Ga,which have an average content of 0.46%,0.015%,0.16 g/t,1.22 g/t,0.0003%,and 0.001%-0.003%,respectively.The ore minerals of this deposit primarily include pyrite,chalcopyrite,bornite,and molybdenite,followed by magnetite,hematite,rutile,gelenite,and sphalerite.The ore-forming fluids of this deposit were magmatic water in the early metallogenic stage and then the mixture of meteoric water and magmatic water at the late metallogenic stage.The ore-forming fluids experienced three stages.The ore-forming fluids of stageⅠhad a hydrochemical type of H_(2)O-CO_(2)-Na Cl,an ore-forming temperature of 375-650℃,and ore-forming pressure of 110-160 MPa.The ore-forming fluids of stageⅡhad a hydrochemical type of H_(2)O-CO_(2)-Na Cl,an ore-forming temperature of 310-350℃,and ore-forming pressure of 58-80 MPa.The ore-forming fluids of stageⅢhad a hydrochemical type of Na Cl-H_(2)O,an ore-forming temperature of 210-290℃,and ore-forming pressure of 5-12 MPa.The CuAu-Mo-Ag mineralization mainly occurred at stagesⅠandⅡ,with the ore-forming materials having a mixed crust-mantle source.The Duobaoshan porphyry Cu deposit was formed in the initial subduction environment of the Paleo-Asian Ocean Plate during the Early Ordovician.Then,due to the closure of the Mongol-Okhotsk Ocean and the subduction and compression of the Paleo-Pacific Ocean,a composite orogenic metallogenic model of the deposit was formed.In other words,it is a porphyry-epithermal copper-gold polymetallic mineralization system of composite orogeny consisting of Paleozoic island arcs and Mesozoic orogeny and extension.