Photoinitiators(PIs), as the key substances for photopolymerized antibacterial film(PAF), affect the cure rate and color of PAF. Herein, two enone dyes were designed and synthesized by a facile approach. Among the can...Photoinitiators(PIs), as the key substances for photopolymerized antibacterial film(PAF), affect the cure rate and color of PAF. Herein, two enone dyes were designed and synthesized by a facile approach. Among the candidates, BDO1 has demonstrated the ability to initiate polymerization of acrylate monomers as single-component PI with the advantages of low mobility, outstanding photobleaching, excellent cytocompatibility, and suitability for light emitting diode(LED) light sources above 365 nm. Taking BDOs as examples, a novel method based on theoretical calculations aiming to assess the potential of enone molecules as single-component PIs was proposed. Finally, under the initiation of BDO1, tannic acid was photopolymerized to a colorless and transparent antibacterial film with high antibacterial ability, which indicated that BDO1 was expected to be used in environmentally friendly PAF.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 viscosity-time curve of a single-component polyurethane(PU)was examined to determine the mixing and compacting temperatures of its mixture and investigate the curing and mechanical properties of single-component P...The viscosity-time curve of a single-component polyurethane(PU)was examined to determine the mixing and compacting temperatures of its mixture and investigate the curing and mechanical properties of single-component PU porous elastic mixture(PPEM).The curing properties of the single-component PU and PPEM were studied with Fourier transform infrared spectroscopy(FTIR)and Marshall test.The mechanical properties of PPEM were explored via the following tests:rutting test,3-point bending test,soaked Marshall stability test,freeze-thaw splitting test,and Cantabro test.The effects of a water bath on the stability of aggregate-PU/asphalt mortar-aggregate systems were evaluated through a pull-out test and a shear test.The results show that the recommended mixing temperatures of toluene diisocyanate and methylene diphenyl diisocyanate range from 75 to 80℃and from 64 to 68℃,respectively.Room temperature(25℃)can be adopted as the compacting temperature of PPEM.PPEM can be fully cured in 4 d.Nevertheless,the water sprinkle method can obviously shorten the full curing time of PPEM.PPEM exhibites good resistance to rutting,brittle cracking,and raveling.The adhesive and shear strength of aggregate-PU/asphalt mortar-aggregate systems are negatively related to water bath duration.展开更多
Single-component organic solar cells(SCOSCs)with high stability and simplified fabrication process are supposed to accelerate the commercialization of organic photovoltaics.However,the types of photo-active materials ...Single-component organic solar cells(SCOSCs)with high stability and simplified fabrication process are supposed to accelerate the commercialization of organic photovoltaics.However,the types of photo-active materials and photovoltaic performance of SCOSCs are still far lagging behind the bulk-heterojunction type organic solar cells(BHJ OSCs).It is still an arduous task to introduce new photo-active materials into SCOSCs,aiming to improve the efficiencies of SCOSCs.One feasible way is to construct double-cable polymers with new structures and tune conformation,morphology and mobility for the improvement in power conversion efficiencies(PCEs).Hence,in this work,we constructed a new double-cable polymer PBTT-BPTI by introducing fused core 5,7-dibromo-2,3-bis(2-ethylhexyl)benzo[1,2-b:4,5-c’]dithiophene-4,8-dione(TTDO)into the main backbone and benzo[ghi]-perylene triimide(BPTI)unit into the side chain.Both of the two units show strong electron-withdrawing property,which are expected to broaden absorption spectra and enhance intermolecular interaction.The double-cable polymer exhibited a broad absorption in the range of 300-700 nm with an optical band gap(E_(g))of 1.79 eV.The PCE of PBTT-BPTI-based SCOSCs was 2.15%,which may be limited by the unconstructed efficient electron transporting channels.展开更多
In this work,the“functionalization-polymerization”(FP)method has been used to construct fullerene-contained double-cable conjugated polymers with“donor-acceptor”backbones.It was realized via synthesizing a fullere...In this work,the“functionalization-polymerization”(FP)method has been used to construct fullerene-contained double-cable conjugated polymers with“donor-acceptor”backbones.It was realized via synthesizing a fullerene-contained monomer and performing Stille polymerization.With this method,a series of double-cable conjugated polymers with different fullerene contents were developed and applied into single-component organic solar cells.The power conversion efficiencies(PCEs)based on these polymers increased from 0.71%to 1.71%with the enhanced fullerene contents.The relatively low PCEs might be originated from the poor microstructure in these polymers.These new conjugated polymers with molecular heterojunction would show potential application in organic electronic devices.展开更多
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
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
Single-component ambipolar polymers are highly desirable for organic electrochem-ical transistors(OECTs)and integration into complementary logic circuits with reduced process complexity.However,they often suffer from ...Single-component ambipolar polymers are highly desirable for organic electrochem-ical transistors(OECTs)and integration into complementary logic circuits with reduced process complexity.However,they often suffer from imbalanced p-type and n-type characteristics and/or stability issues.Herein,a novel single-component ambipolar polymer,namely,gIDT–BBT is reported based on indacenodithiophene(IDT)as the electron donor,benzobisthiadiazole(BBT)as the electron acceptor and oligo ethylene glycol(OEG)as the side chain.Benefitting from the extended backbone planarity and rigidity of IDT,pronounced electron-withdrawing capabil-ity of BBT,favored ionic transport from OEG together with vertical OECT device structure,a nearly balanced ambipolar OECT performance is achieved for gIDT–BBT,revealing a high transconductance of 155.05±1.58/27.28±0.92 mS,a high current on/off ratio>10^(6) and an excellent operational stability under both p-type and n-type operation conditions.With gIDT–BBT in hand,furthermore,vertically stacked complementary inverters are successfully fabricated to show a maximum voltage gain of 28 V V^(-1)(V_(IN)=0.9 V)and stable operation over 1000 switching cycles,and then used for efficient electrooculogram recording.This work provides a new approach for the development of ambipolar single-component organic mixed ionic–electronic conductors and establishes a foundation for the manufacture of high-performance ambipolar OECTs and associated complementary circuits.展开更多
White-light emitting(WLE) polymers have attracted continuous attention for their promising applications in solid-state lighting,flexible display and related fields. However, achieving dual-emission and pure white-ligh...White-light emitting(WLE) polymers have attracted continuous attention for their promising applications in solid-state lighting,flexible display and related fields. However, achieving dual-emission and pure white-light emission in a single-component polymer is still challenging. In this study, a brominated single-component polymer Br OD-TFB was designed and synthesized,which shows dual-emission and white light emission properties in solution and room-temperature phosphorescence(RTP) in thin films. The dual-emission properties can be tuned by concentration, solvent polarity, and excitation energy. Spectral analyses and theoretical calculations reveal that the origin of the high-energy emission band(HEB) is intramolecular charge transfer(ICT)along the polymer chain, whilst the low-energy emission band(LEB) originates from the excited-state related to the intra-chain and inter-chain C–Br···π interactions as demonstrated by the single-crystal structure of the model compound. Appropriate control of the formation and the destruction of the halogen-assisted interactions can initiate white-light emission in the singlecomponent polymer. More interestingly, by dispersing Br OD-TFB(0.1 wt%) in a non-emissive, colorless and transparent polymer, the characteristics of this white-light emission can be fully demonstrated while exhibiting unexpected RTP properties,with photoluminescence quantum efficiency(Φ_(PL)) of up to 23% and CIE coordinates of(0.32, 0.32).展开更多
The development of single-component white emitters for white light-emitting diodes(WLEDs)remains challenging.Herein,a rare earth-free white light-emitting composite is developed by assembling blue-emitting carbon dots...The development of single-component white emitters for white light-emitting diodes(WLEDs)remains challenging.Herein,a rare earth-free white light-emitting composite is developed by assembling blue-emitting carbon dots(CDs)and yellow-emitting Cs_(2)InCl_(5)·H_(2)O:Sb^(3+)metal halide crystals via a facile liquid-liquid diffusion-assisted crystallization approach.The encapsulation mechanism is then analyzed.Depending on the ratios of blue/yellow emitters,these luminescent composites exhibit white light emission with tunable cold and warm hues.The composites also possess prominent ultraviolet resistance,thermal tolerance,and good stability at about 200°C.By employing such“CDs in metal halide”composites as a converter,a WLED is successfully fabricated with a high color rendering index of 93.6,benefiting from the assembled blue and yellow broadband emission.With this strategy,the developed composites show great promise in next-generation WLED lighting.展开更多
Materials showing metallophilic interactions continue to attract considerable theoretical and experimental attention largely because of their unusual and unanticipated photophysical behavior as well as their unique st...Materials showing metallophilic interactions continue to attract considerable theoretical and experimental attention largely because of their unusual and unanticipated photophysical behavior as well as their unique stimuli-responsive behavior in an aggregate or solid state.Metallophilic interactions are mostly found between metals with either identical(d^(10)–d^(10))or different(s^(2)–d^(8),d^(8)–d^(10))configurations.Among various metallophilic interactions,aurophilic interactions(Au⋯Au)are well-known and widely reported.In this study,a new phosphorescent gold(I)complex,[(CF_(3)Ph)_(3)PAuC≡CPh](TPPGPA)was reported.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
In the realm of nonlinear integrable systems,the presence of decompositions facilitates the establishment of linear superposition solutions and the derivation of novel coupled systems exhibiting nonlinear integrabilit...In the realm of nonlinear integrable systems,the presence of decompositions facilitates the establishment of linear superposition solutions and the derivation of novel coupled systems exhibiting nonlinear integrability.By focusing on single-component decompositions within the potential BKP hierarchy,it has been observed that specific linear superpositions of decomposition solutions remain consistent with the underlying equations.Moreover,through the implementation of multi-component decompositions within the potential BKP hierarchy,successful endeavors have been undertaken to formulate linear superposition solutions and novel coupled Kd V-type systems that resist decoupling via alterations in dependent variables.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
The device configuration with mesoporous titanium dioxide(m-TiO2)has garnered considerable attention as a promising solution for high-stable perovskite and dye-sensitized solar cells,although its application in organi...The device configuration with mesoporous titanium dioxide(m-TiO2)has garnered considerable attention as a promising solution for high-stable perovskite and dye-sensitized solar cells,although its application in organic solar cells remains unexplored.In this communication,we have incorporated this structure into both bulk-heterojunction(BHJ)and single-component organic solar cells(SCOSCs).Surprisingly,mesoporous OSCs(M-OSCs)demonstrate a deteriorative efficiency in BHJ-type cells,whereas this configuration succeeds in SCOSCs,exhibiting competitive performance with planar OSCs(P-OSCs).This pioneering study has resulted in a competitive power conversion efficiency of 9.67%for m-TiO_(2)-based cells,marking a significant milestone in the advancement of OSCs.Importantly,profiting from the better ultraviolet resistance of m-TiO_(2)than zinc oxide,this M-OSC exhibits superior photostability than that of P-OSCs when subjected to continuous one-sun(AM1.5G)illumination.In its entirety,this research not only introduces the concept of M-OSCs for the first time but also unveils a novel device architecture poised to address the long-term stability concerns within the realm of OSCs.展开更多
A series of single-composition emission-tunable CdWO4：Eu^3＋ uniform size nanorods were synthesized by polyvinylpyrrolidone（PVP） assisted hydrothermal process. The products were measured by powder X-ray diffraction...A series of single-composition emission-tunable CdWO4：Eu^3＋ uniform size nanorods were synthesized by polyvinylpyrrolidone（PVP） assisted hydrothermal process. The products were measured by powder X-ray diffraction（PXRD）, scanning electron microscopy（SEM）, transmission electron microscopy（TEM）, photoluminescence, and fluorescent decay test. The results showed that reaction time, temperature, p H values and Eu^3＋ doped concentration played important roles in determining the morphologies and photoluminescent properties. And we also investigated its use in Ga N LED, warm-white-light could be obtained by the combination of the bright blue light originated from the charge transfer transition in the tungstate groups and the near UV light from LED chip with the red emission from 4f-4f transition of Eu^3＋, respectively. By properly tuning the doping concentration of Eu^3＋, chromaticity coordinates（0.30 0.22） could be achieved under the 380 nm excitation and its color rendering index was 80.6. So it has potential application in warm-WLED and replacing the commercial YAG：Ce phosphor which absence of red band emission.展开更多
A series of o-phenylenediamine bridged tris(phenolate)ligand-stabilized rare-earth metal complexes were synthesized and characterized.Lanthanum(complex 1),neodymium(complex 2^(tBu)),and yttrium(complex 3)complexes sta...A series of o-phenylenediamine bridged tris(phenolate)ligand-stabilized rare-earth metal complexes were synthesized and characterized.Lanthanum(complex 1),neodymium(complex 2^(tBu)),and yttrium(complex 3)complexes stabilized by ligand of buiky tert-butyl substituents are mononuclear,whereas neodymium complexes 2^(Me)and 2^(C1)bearing smaller methyl and chloro substituents are dinuclear,respectively.They were applied in the alternating copolymerization of CO_(2)and cyclohexene oxide.The addition of benzyl alcohol is beneficial to improving yields(up to 86%)and selectivity of poly(carbonate)(up to 99%).Stoichiometric reaction of benzyl alcohol with rare-earth metal complexes 1 and 2^(tBu)results in formation of complexes 4 and 5 as dinuclear complexes with benzyl alcohol coordination,which was confirmed via single crystal X-ray diffraction analysis,and nuclear magnetic resonance(NMR)spectroscopy(for 4).Complex 5 shows equally good activity and selectivity of that of complex 2^(tBu)and benzyl alcohol,consolidating that complex 5 is indeed generated during polymerization.The neodymium tris(phenolate)5 is one of the few examples of rare-earth metal complex as a single-component initiator for copolymerization of epoxide and CO_(2).Matrix-assisted laser desorption ionization-time of flight(MALDI-TOF)mass spectrometry analysis proves benzyloxy group as the chain end.^(1)H NMR monitoring suggests that the insertion of CO_(2)may be the first step in the growth of the polymer chain.展开更多
Fluorine substitution was applied to the donor and acceptor segments of block copolymers to understand the impact of molecular structure on photovoltaic block copolymers and explore efficient materials for single-comp...Fluorine substitution was applied to the donor and acceptor segments of block copolymers to understand the impact of molecular structure on photovoltaic block copolymers and explore efficient materials for single-component organic solar cells(SCOSCs).Along this line,three fluorinated block copolymers,namely PBDB-T-b-PTYF6,PM6-b-PTY6,and PM6-bPTYF6,derived from PBDB-T-b-PTY6 were designed and synthesized.The UV-Vis absorption,energy level,and thin-film morphology of these block copolymers were systematically characterized.All fluorinated block copolymers show narrow bandgap and improved crystallinity.An enhanced open-circuit voltage was observed in the SCOSC based on PM6-b-PTY6.However,SCOSCs based on all fluorinated block copolymers exhibited low short-circuit current due to energy level mismatch and therefore had low power conversion efficiency at around 4%.By contrast,the SCOSCs based on control block copolymer PBDB-T-b-PTY6 exhibited the highest power conversion efficiency approaching 10%,with a high short-circuit current of 18.57 mA/cm~2.Our study was the first to perform fluorination on photovoltaic block copolymers and provides insight into precisely controlling the polymer structure and understanding the structure-property relationship in SCOSCs based on block copolymers.展开更多
Colloidal chemical synthesis of various types of magnetic nanocrystals is discussed with regard to recent discoveries. We first outline the chemical preparation of single-component magnetic nanocrystals with controlle...Colloidal chemical synthesis of various types of magnetic nanocrystals is discussed with regard to recent discoveries. We first outline the chemical preparation of single-component magnetic nanocrystals with controlled size, shape, and uniformity based on several solution-phase methods, especially thermal decomposition and/or reduction method. Then we discuss the synthetic strategies of multi-component nanocrystals incorporating at least one magnetic component by manipulating heterogeneous nucleation and growth process. Toward the end, approaches for preparing hollow/porous magnetic nanocrystals are highlighted. We believe that the summarized chemical synthesis will pave the way for the future development of extraordinary magnetic nanocrystals.展开更多
基金financially supported by National Natural Science Foundation of China (Nos. 21925802, 22338005)Liaoning Binhai Laboratory (No. LBLB-2023–03)the Fundamental Research Funds for the Central Universities (No. DUT22LAB601)。
文摘Photoinitiators(PIs), as the key substances for photopolymerized antibacterial film(PAF), affect the cure rate and color of PAF. Herein, two enone dyes were designed and synthesized by a facile approach. Among the candidates, BDO1 has demonstrated the ability to initiate polymerization of acrylate monomers as single-component PI with the advantages of low mobility, outstanding photobleaching, excellent cytocompatibility, and suitability for light emitting diode(LED) light sources above 365 nm. Taking BDOs as examples, a novel method based on theoretical calculations aiming to assess the potential of enone molecules as single-component PIs was proposed. Finally, under the initiation of BDO1, tannic acid was photopolymerized to a colorless and transparent antibacterial film with high antibacterial ability, which indicated that BDO1 was expected to be used in environmentally friendly PAF.
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The Fundamental Research Funds for the Central Research Institute (No. 2020-9054)。
文摘The viscosity-time curve of a single-component polyurethane(PU)was examined to determine the mixing and compacting temperatures of its mixture and investigate the curing and mechanical properties of single-component PU porous elastic mixture(PPEM).The curing properties of the single-component PU and PPEM were studied with Fourier transform infrared spectroscopy(FTIR)and Marshall test.The mechanical properties of PPEM were explored via the following tests:rutting test,3-point bending test,soaked Marshall stability test,freeze-thaw splitting test,and Cantabro test.The effects of a water bath on the stability of aggregate-PU/asphalt mortar-aggregate systems were evaluated through a pull-out test and a shear test.The results show that the recommended mixing temperatures of toluene diisocyanate and methylene diphenyl diisocyanate range from 75 to 80℃and from 64 to 68℃,respectively.Room temperature(25℃)can be adopted as the compacting temperature of PPEM.PPEM can be fully cured in 4 d.Nevertheless,the water sprinkle method can obviously shorten the full curing time of PPEM.PPEM exhibites good resistance to rutting,brittle cracking,and raveling.The adhesive and shear strength of aggregate-PU/asphalt mortar-aggregate systems are negatively related to water bath duration.
基金jointly supported by National Key R&D Program of China(Nos.2018YFA0208504,2017YFA0204702)National Natural Science Foundation of China(Nos.51773207,21574138,21905018)+2 种基金Natural Science Foundation of Hebei Province(No.B2020201032)further supported by the Fundamental Research Funds for the Central Universities(No.XK1802-2)Open Project of State Key Laboratory of Supramolecular Structure and Materials(No.sklssm202043)。
文摘Single-component organic solar cells(SCOSCs)with high stability and simplified fabrication process are supposed to accelerate the commercialization of organic photovoltaics.However,the types of photo-active materials and photovoltaic performance of SCOSCs are still far lagging behind the bulk-heterojunction type organic solar cells(BHJ OSCs).It is still an arduous task to introduce new photo-active materials into SCOSCs,aiming to improve the efficiencies of SCOSCs.One feasible way is to construct double-cable polymers with new structures and tune conformation,morphology and mobility for the improvement in power conversion efficiencies(PCEs).Hence,in this work,we constructed a new double-cable polymer PBTT-BPTI by introducing fused core 5,7-dibromo-2,3-bis(2-ethylhexyl)benzo[1,2-b:4,5-c’]dithiophene-4,8-dione(TTDO)into the main backbone and benzo[ghi]-perylene triimide(BPTI)unit into the side chain.Both of the two units show strong electron-withdrawing property,which are expected to broaden absorption spectra and enhance intermolecular interaction.The double-cable polymer exhibited a broad absorption in the range of 300-700 nm with an optical band gap(E_(g))of 1.79 eV.The PCE of PBTT-BPTI-based SCOSCs was 2.15%,which may be limited by the unconstructed efficient electron transporting channels.
基金This study was financially supported by Beijing Natural Science Foundation of China.(No.JQ21006)the National Natural Science Foundation of China(Nos.92163128,52073016,51773207,21905018 and 21905158)of China+2 种基金This work was further financially supported by the Fundamental Research Funds for the Central Universities(Nos.buctrc201828 and XK1802-2)the opening Foundation of State Key Laboratory of Organic-Inorganic Composites,Beijing University of Chemical Technology(No.oic-202201006)Jiangxi Provincial Department of Science and Technology(No.20192ACB20009).
文摘In this work,the“functionalization-polymerization”(FP)method has been used to construct fullerene-contained double-cable conjugated polymers with“donor-acceptor”backbones.It was realized via synthesizing a fullerene-contained monomer and performing Stille polymerization.With this method,a series of double-cable conjugated polymers with different fullerene contents were developed and applied into single-component organic solar cells.The power conversion efficiencies(PCEs)based on these polymers increased from 0.71%to 1.71%with the enhanced fullerene contents.The relatively low PCEs might be originated from the poor microstructure in these polymers.These new conjugated polymers with molecular heterojunction would show potential application in organic electronic devices.
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 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Sichuan Science and Technology Program,Grant/Award Number:2023ZYD0161Chengdu Science and Technology Bureau,Grant/Award Number:2023-YF06-00028-HZ+5 种基金National Natural Science Foundation of China,Grant/Award Numbers:92163132,52263019,52273316,62273073Yunnan Fundamental Research Project,Grant/Award Number:202301AT070313Yunling Scholar Project of“Yunnan Revitalization Talent Support Program”National Key Research and Development Program of China,Grant/Award Numbers:2022YFE0134800,2023YFC2411800Aeronautical Science Foundation of China,Grant/Award Number:20230024080002Yunnan Provincial Department of Education Science Research Fund Graduate Program,Grant/Award Number:2023Y0236。
文摘Single-component ambipolar polymers are highly desirable for organic electrochem-ical transistors(OECTs)and integration into complementary logic circuits with reduced process complexity.However,they often suffer from imbalanced p-type and n-type characteristics and/or stability issues.Herein,a novel single-component ambipolar polymer,namely,gIDT–BBT is reported based on indacenodithiophene(IDT)as the electron donor,benzobisthiadiazole(BBT)as the electron acceptor and oligo ethylene glycol(OEG)as the side chain.Benefitting from the extended backbone planarity and rigidity of IDT,pronounced electron-withdrawing capabil-ity of BBT,favored ionic transport from OEG together with vertical OECT device structure,a nearly balanced ambipolar OECT performance is achieved for gIDT–BBT,revealing a high transconductance of 155.05±1.58/27.28±0.92 mS,a high current on/off ratio>10^(6) and an excellent operational stability under both p-type and n-type operation conditions.With gIDT–BBT in hand,furthermore,vertically stacked complementary inverters are successfully fabricated to show a maximum voltage gain of 28 V V^(-1)(V_(IN)=0.9 V)and stable operation over 1000 switching cycles,and then used for efficient electrooculogram recording.This work provides a new approach for the development of ambipolar single-component organic mixed ionic–electronic conductors and establishes a foundation for the manufacture of high-performance ambipolar OECTs and associated complementary circuits.
基金supported by the National Natural Science Foundation of China(51873239,51373204,U20A20255)the Science and Technology Project of Guangdong Province(2015B090915003,2019B040401002,2020B010182001)+2 种基金National Basic Research Program of China(2014CB643605)the Leading Scientific,Technical and Innovation Talents of Guangdong Special Support Program(2016TX03C295)the Natural Science Foundation of Guangdong Province(2114050001078)。
文摘White-light emitting(WLE) polymers have attracted continuous attention for their promising applications in solid-state lighting,flexible display and related fields. However, achieving dual-emission and pure white-light emission in a single-component polymer is still challenging. In this study, a brominated single-component polymer Br OD-TFB was designed and synthesized,which shows dual-emission and white light emission properties in solution and room-temperature phosphorescence(RTP) in thin films. The dual-emission properties can be tuned by concentration, solvent polarity, and excitation energy. Spectral analyses and theoretical calculations reveal that the origin of the high-energy emission band(HEB) is intramolecular charge transfer(ICT)along the polymer chain, whilst the low-energy emission band(LEB) originates from the excited-state related to the intra-chain and inter-chain C–Br···π interactions as demonstrated by the single-crystal structure of the model compound. Appropriate control of the formation and the destruction of the halogen-assisted interactions can initiate white-light emission in the singlecomponent polymer. More interestingly, by dispersing Br OD-TFB(0.1 wt%) in a non-emissive, colorless and transparent polymer, the characteristics of this white-light emission can be fully demonstrated while exhibiting unexpected RTP properties,with photoluminescence quantum efficiency(Φ_(PL)) of up to 23% and CIE coordinates of(0.32, 0.32).
基金supported by the National Natural Science Foundations of China (51961145101)Guangzhou Science & Technology Project (202007020005)+3 种基金the Project Supported by Guangdong Province Universities and Colleges Pearl River Scholar Funded Scheme (GDUPS, 2018) for Prof. Bingfu Leithe National Key R&D Program of China (2020YFB0407902)Guangdong Provincial Science & Technology Project (2021A0505050006 and 2021B0707010003)Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Teams (2021KJ122)。
文摘The development of single-component white emitters for white light-emitting diodes(WLEDs)remains challenging.Herein,a rare earth-free white light-emitting composite is developed by assembling blue-emitting carbon dots(CDs)and yellow-emitting Cs_(2)InCl_(5)·H_(2)O:Sb^(3+)metal halide crystals via a facile liquid-liquid diffusion-assisted crystallization approach.The encapsulation mechanism is then analyzed.Depending on the ratios of blue/yellow emitters,these luminescent composites exhibit white light emission with tunable cold and warm hues.The composites also possess prominent ultraviolet resistance,thermal tolerance,and good stability at about 200°C.By employing such“CDs in metal halide”composites as a converter,a WLED is successfully fabricated with a high color rendering index of 93.6,benefiting from the assembled blue and yellow broadband emission.With this strategy,the developed composites show great promise in next-generation WLED lighting.
基金supported by the National Natural Science Foundation of China(no.21788102)the Natural Science Foundation of Guangdong Province(nos.2019B121205002 and 2019B030301003)+1 种基金the Research Grants Council of Hong Kong(nos.16305618,16305518,16304819,C6009-17G,and C6014-20W)the Innovation and Technology Commission(no.ITC-CNERC14SC01).
文摘Materials showing metallophilic interactions continue to attract considerable theoretical and experimental attention largely because of their unusual and unanticipated photophysical behavior as well as their unique stimuli-responsive behavior in an aggregate or solid state.Metallophilic interactions are mostly found between metals with either identical(d^(10)–d^(10))or different(s^(2)–d^(8),d^(8)–d^(10))configurations.Among various metallophilic interactions,aurophilic interactions(Au⋯Au)are well-known and widely reported.In this study,a new phosphorescent gold(I)complex,[(CF_(3)Ph)_(3)PAuC≡CPh](TPPGPA)was reported.
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sponsored by the National Natural Science Foundations of China under Grant Nos.12301315,12235007,11975131the Zhejiang Provincial Natural Science Foundation of China under Grant No.LQ20A010009。
文摘In the realm of nonlinear integrable systems,the presence of decompositions facilitates the establishment of linear superposition solutions and the derivation of novel coupled systems exhibiting nonlinear integrability.By focusing on single-component decompositions within the potential BKP hierarchy,it has been observed that specific linear superpositions of decomposition solutions remain consistent with the underlying equations.Moreover,through the implementation of multi-component decompositions within the potential BKP hierarchy,successful endeavors have been undertaken to formulate linear superposition solutions and novel coupled Kd V-type systems that resist decoupling via alterations in dependent variables.
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jointly supported by the Natural Science Special Foundation of Guizhou University(No.GZUTGH[2023]71)the Beijing Natural Science Foundation(No.JQ21006)+3 种基金the National Natural Science Foundation of China(Nos.92163128,52073016)further supported by the 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.sklssm2023010)。
文摘The device configuration with mesoporous titanium dioxide(m-TiO2)has garnered considerable attention as a promising solution for high-stable perovskite and dye-sensitized solar cells,although its application in organic solar cells remains unexplored.In this communication,we have incorporated this structure into both bulk-heterojunction(BHJ)and single-component organic solar cells(SCOSCs).Surprisingly,mesoporous OSCs(M-OSCs)demonstrate a deteriorative efficiency in BHJ-type cells,whereas this configuration succeeds in SCOSCs,exhibiting competitive performance with planar OSCs(P-OSCs).This pioneering study has resulted in a competitive power conversion efficiency of 9.67%for m-TiO_(2)-based cells,marking a significant milestone in the advancement of OSCs.Importantly,profiting from the better ultraviolet resistance of m-TiO_(2)than zinc oxide,this M-OSC exhibits superior photostability than that of P-OSCs when subjected to continuous one-sun(AM1.5G)illumination.In its entirety,this research not only introduces the concept of M-OSCs for the first time but also unveils a novel device architecture poised to address the long-term stability concerns within the realm of OSCs.
基金Project supported by the National Natural Science Foundation of China(21301115)the Shanghai University Innovation Fund(sdcx2012005)Funding Scheme for Training Young Teachers in Colleges and Universities(ZZSD12025)
文摘A series of single-composition emission-tunable CdWO4：Eu^3＋ uniform size nanorods were synthesized by polyvinylpyrrolidone（PVP） assisted hydrothermal process. The products were measured by powder X-ray diffraction（PXRD）, scanning electron microscopy（SEM）, transmission electron microscopy（TEM）, photoluminescence, and fluorescent decay test. The results showed that reaction time, temperature, p H values and Eu^3＋ doped concentration played important roles in determining the morphologies and photoluminescent properties. And we also investigated its use in Ga N LED, warm-white-light could be obtained by the combination of the bright blue light originated from the charge transfer transition in the tungstate groups and the near UV light from LED chip with the red emission from 4f-4f transition of Eu^3＋, respectively. By properly tuning the doping concentration of Eu^3＋, chromaticity coordinates（0.30 0.22） could be achieved under the 380 nm excitation and its color rendering index was 80.6. So it has potential application in warm-WLED and replacing the commercial YAG：Ce phosphor which absence of red band emission.
基金Project supported by the National Natural Science Foundation of China(21871198)the Major Research Project of the Natural Science of the Jiangsu Higher Education Institutions(19KJA360005)the Open Research Fund of State Key Laboratory of Rare-Earth Resource Utilization(CIAC)and PAPD。
文摘A series of o-phenylenediamine bridged tris(phenolate)ligand-stabilized rare-earth metal complexes were synthesized and characterized.Lanthanum(complex 1),neodymium(complex 2^(tBu)),and yttrium(complex 3)complexes stabilized by ligand of buiky tert-butyl substituents are mononuclear,whereas neodymium complexes 2^(Me)and 2^(C1)bearing smaller methyl and chloro substituents are dinuclear,respectively.They were applied in the alternating copolymerization of CO_(2)and cyclohexene oxide.The addition of benzyl alcohol is beneficial to improving yields(up to 86%)and selectivity of poly(carbonate)(up to 99%).Stoichiometric reaction of benzyl alcohol with rare-earth metal complexes 1 and 2^(tBu)results in formation of complexes 4 and 5 as dinuclear complexes with benzyl alcohol coordination,which was confirmed via single crystal X-ray diffraction analysis,and nuclear magnetic resonance(NMR)spectroscopy(for 4).Complex 5 shows equally good activity and selectivity of that of complex 2^(tBu)and benzyl alcohol,consolidating that complex 5 is indeed generated during polymerization.The neodymium tris(phenolate)5 is one of the few examples of rare-earth metal complex as a single-component initiator for copolymerization of epoxide and CO_(2).Matrix-assisted laser desorption ionization-time of flight(MALDI-TOF)mass spectrometry analysis proves benzyloxy group as the chain end.^(1)H NMR monitoring suggests that the insertion of CO_(2)may be the first step in the growth of the polymer chain.
基金supported by the National Natural Science Foundation of China(No.52073198)Science Foundation of Jiangsu Province(BK20211598)+1 种基金“111”project,the China Postdoctoral Science Foundation(No.2021T140495),Collaborative Innovation Center of Suzhou Nano Science and Technology,Soochow Universitythe Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)。
文摘Fluorine substitution was applied to the donor and acceptor segments of block copolymers to understand the impact of molecular structure on photovoltaic block copolymers and explore efficient materials for single-component organic solar cells(SCOSCs).Along this line,three fluorinated block copolymers,namely PBDB-T-b-PTYF6,PM6-b-PTY6,and PM6-bPTYF6,derived from PBDB-T-b-PTY6 were designed and synthesized.The UV-Vis absorption,energy level,and thin-film morphology of these block copolymers were systematically characterized.All fluorinated block copolymers show narrow bandgap and improved crystallinity.An enhanced open-circuit voltage was observed in the SCOSC based on PM6-b-PTY6.However,SCOSCs based on all fluorinated block copolymers exhibited low short-circuit current due to energy level mismatch and therefore had low power conversion efficiency at around 4%.By contrast,the SCOSCs based on control block copolymer PBDB-T-b-PTY6 exhibited the highest power conversion efficiency approaching 10%,with a high short-circuit current of 18.57 mA/cm~2.Our study was the first to perform fluorination on photovoltaic block copolymers and provides insight into precisely controlling the polymer structure and understanding the structure-property relationship in SCOSCs based on block copolymers.
基金Project supported by the National Basic Research Program of China(Grant No.2010CB934601)the National Natural Science Foundation of China(Grant Nos.51125001,51172005,and 90922033)+4 种基金the Natural Science Foundation of Beijing(Grant No.2122022)the Doctoral Program Foundation(Grant No.20120001110078)the New Century Talent Foundation of the Education Ministry of China(Grant No.NCET-09-0177)the Yok Ying Tung Foundation(Grant No.122043)the PKU COE-Health Science Center Seed Fund
文摘Colloidal chemical synthesis of various types of magnetic nanocrystals is discussed with regard to recent discoveries. We first outline the chemical preparation of single-component magnetic nanocrystals with controlled size, shape, and uniformity based on several solution-phase methods, especially thermal decomposition and/or reduction method. Then we discuss the synthetic strategies of multi-component nanocrystals incorporating at least one magnetic component by manipulating heterogeneous nucleation and growth process. Toward the end, approaches for preparing hollow/porous magnetic nanocrystals are highlighted. We believe that the summarized chemical synthesis will pave the way for the future development of extraordinary magnetic nanocrystals.
