Polyimide(PI)is widely used in high-frequency communication technology due to its exceptional comprehensive properties.However,traditional PI has a relatively elevated dielectric constant and dielectric loss.Herein,th...Polyimide(PI)is widely used in high-frequency communication technology due to its exceptional comprehensive properties.However,traditional PI has a relatively elevated dielectric constant and dielectric loss.Herein,the different cross-linked structures were introduced in PI matrix and conducted a detailed discussion on the influence of cross-linking agent content and cross-linking structure type on the overall performance of PI films.In comparison to the dielectric constant of 2.9 of neat PI,PI with an interchain cross-linking structure containing 2 wt%1,3,5-tris(4-aminophenyl)benzene(TAPB)(interchain-PI-2)exhibited the reduced dielectric constant of 2.55 at 1 MHz.The PI films with intrachain crosslinking structure containing 2 wt%TAPB(intrachain-PI-2)exhibited the lowest dielectric constant of 2.35 and the minimum dielectric loss of0.0075 at 1 MHz.It was due to the more entanglement junctions of intrachain-PI resulting in decreased carrier transport.The thermal expansion coefficients of both interchain-PI and intrachain-PI films were effectively reduced.Moreover,in contrast to interchain-PI films,the intrachain-PI films maintained colorlessness and transparency as the cross-linking agent content increased.This work compared the effects of two different cross-linked structures on the performance of PI films and provided a feasible way to obtain low-k PI films with excellent comprehensive performance for 5G applications.展开更多
Bulk heterojunction(BHJ)composites show improved power conversion efficiencies when optimized in terms of morphology using various film processing methods.A reduced carrier recombination loss in an optimized BHJ was c...Bulk heterojunction(BHJ)composites show improved power conversion efficiencies when optimized in terms of morphology using various film processing methods.A reduced carrier recombination loss in an optimized BHJ was characterized previously.However,the driving force that leads to this reduction was not clearly understood.In this study,we focus on the decreased carrier recombination loss and its driving force in optimized nonfullerene acceptor-based PTB7-Th:IEICO-4F BHJ composites.We demonstrate that the optimized BHJ shows deactivation in the sub-nanosecond nongeminate carrier recombination process.The driving force for this deactivation was determined to be the improved interchain hole delocalization between the polymers.An enhanced interchain hole delocalization was observed using steady-state photoinduced absorption(PIA)spectroscopy.In particular,increased splitting between the polaron PIA bands was noted.Moreover,improved interchain hole delocalization was observed for other state-of-the-art BHJ materials,including D18:Y6 with optimized morphologies.展开更多
We propose a novel approach to generate and manipulate topological Floquet bound states in the continuum(BICs)via a class of systems constructed by coupling two identical periodically driven one-dimensional Su-Schrief...We propose a novel approach to generate and manipulate topological Floquet bound states in the continuum(BICs)via a class of systems constructed by coupling two identical periodically driven one-dimensional Su-Schrieffer-Heeger chains.The formation of topological Floquet BICs can be adjusted only by tuning the driving amplitude or frequency,regardless of whether the static system has BICs or not.The interchain bias can only change the localization property of topological Floquet BICs,and a bigger bias can lead to transforming topological Floquet BICs into bound states out of the continuum(BOCs).But it does not change the topological properties of these topological Floquet states.Based on the repulsion effect of edge states,we propose to detect occurrence of topological Floquet BICs and transition point between topological Floquet BICs and BOCs using quantum walk.Our work provided a convenient and realistic approach for the experimental realization and manipulation of BICs in a single-particle quantum system.展开更多
Polaron dynamics in a system of highly ordered conjugated polymer chains is investigated based on the tight binding model. With the interchain coupling enhancing,it takes longer time for the electron added to the syst...Polaron dynamics in a system of highly ordered conjugated polymer chains is investigated based on the tight binding model. With the interchain coupling enhancing,it takes longer time for the electron added to the system to induce a localized polaron state. Beyond a certain strength of the interchain coupling,the electron evolves into a two-dimensional delocalized polaron state. Dynamical simulations suggest that the well-ordered organic molecule systems with two-dimensional polarons exhibit higher mobilities than the systems with intrachain localized polarons,as also suggested by earlier experiments.展开更多
The photoluminescence(PL) properties of poly[ (2, 5 - diphenylene - 1, 3, 4 - oxadiazole) - 4, 4’ - viny-lene] (O - PPV) are investigated using absorption and excitation measurements for different concentration ratio...The photoluminescence(PL) properties of poly[ (2, 5 - diphenylene - 1, 3, 4 - oxadiazole) - 4, 4’ - viny-lene] (O - PPV) are investigated using absorption and excitation measurements for different concentration ratios of solid-state O - PPV/ PEO (polyethylene oxide ) blends, as well as by comparing PL spectra for dilute solution and solid state pristine O - PPV. The solid film of O - PPV/PEO is prepared to investigate the interaction between polymers. The O - PPV molecules are dispersed into PEO which is used as a inert material in order to change the interaction between O - PPV. In the O -PPV/PEO blends, it is found that the PL spectra excited by 300nm for different concentration ratios are different. There are three peaks in the PL spectra of 1: 100 and 1: 200 (O - PPV/PEO) blends, and the relative intensities of peaks at 500nm and 460nm gradually decrease with lowering the concentrations of O - PPV. There leaves one peak at 416nm when the ratio of O - PPV to PEO is below 1: 300, and PL shape does not change any longer. The results show that the solid-state O - PPV emission arises from interchain charge-transfer states due to interchain effects.According to the absorption and photoluminescence spectra of the solid films, it is also believed that there are types of localized and delocalized states in conjugated polymers. The two types of states have different effects on charge-transfer state in different concentrations of solid films.展开更多
Type Ⅰ Ⅲ and Ⅴ collagens were extracted from bovine dermis and cornea by using pepsin treatment in acetic acid solution, followed by salt precipitation and dialysis, to purify and isolate each type of collagens. Th...Type Ⅰ Ⅲ and Ⅴ collagens were extracted from bovine dermis and cornea by using pepsin treatment in acetic acid solution, followed by salt precipitation and dialysis, to purify and isolate each type of collagens. The preparation process was analyzed by using sodium dodecyl sulfate polyacrylamide gel electrophoresis （SDS-PAGE）. A reducing agent, 2-mercaptoethanol, was used to remove disulfide bonds and analyze the structure of the bonds involved between α chains in some types of collagens. The use of delayed reducing methods resulted in the difference between α1 （Ⅲ） and α1 （ Ⅰ ） chains in a mixture containing type Ⅰ and Ⅲ collagens. The structure of disulfide bonds among α chains exists potentially in type V collagen prepared from the pepsin-treatment extraction at 4 ℃, which differs from type Ⅲ collagen in relation to the locations of disulfide bonds. Compared with pepsin-treated collagen at 4 ℃, the relative molecular weights of α1 （V） and α2 （V） chains treated at room temperature decrease by 4.6% and 6.0%, respectively. It is concluded that type Ⅰ Ⅲ and Ⅴ collagens can be prepared from bovine dermis and cornea by the use of pepsin treatment, salt precipitation and dialysis. The interchain disulfide bonds lie potentially near the edges of termini of type V collagen molecules in extracellular matrix, and a small number of interchain crosslinks exist in type V collagen.展开更多
The Peierls structural transition in quasi-one-dimensional organic crystals of TTF-TCNQ is investigated in the frame of a more complete physical model. The two most important electron-phonon interaction mechanisms are...The Peierls structural transition in quasi-one-dimensional organic crystals of TTF-TCNQ is investigated in the frame of a more complete physical model. The two most important electron-phonon interaction mechanisms are taken into account simultaneously. One is similar of that of deformation potential and the other is of polaron type. For simplicity, the 2D crystal model is considered. The renormalized phonon spectrum and the phonon polarization operator are calculated in the random phase approximation for different temperatures. The effects of interchain interaction on renormalized acoustic phonons and on the Peierls critical temperature are analyzed.展开更多
We investigate the metal-insulator transition in quasi-one-dimensional organic crystals of tetrathiotetracene-iodide, TTT2I3, in the 2D model. A crystal physical model is applied which takes into account two the most ...We investigate the metal-insulator transition in quasi-one-dimensional organic crystals of tetrathiotetracene-iodide, TTT2I3, in the 2D model. A crystal physical model is applied which takes into account two the most important hole-phonon interaction mechanisms. One is similar to that of deformation potential and the other is of polaron type. The scattering on defects is also considered and it is crucial for the explanation of the transition. The phonon polarization operator and the renormalized phonon spectrum are calculated in the random phase approximation for different temperatures applying the method of Green functions. We show that the transition is of Peierls type. The effect of lattice distortion on the dispersion of renormalized acoustic phonons is analyzed.展开更多
The Peierls structural transition in the TTT<sub>2</sub>I<sub>3</sub> (tetrathiotetracene-iodide) crystal, for different values of carrier concentration is studied in 3D approximation. A crysta...The Peierls structural transition in the TTT<sub>2</sub>I<sub>3</sub> (tetrathiotetracene-iodide) crystal, for different values of carrier concentration is studied in 3D approximation. A crystal physical model is applied that considers two of the most important hole-phonon interactions. The first interaction describes the deformation potential and the second one is of polaron type. In the presented physical model, the interaction of carriers with the structural defects is taken into account. This is crucial for the explanation of the transition. The renormalized phonon spectrum is calculated in the random phase approximation for different temperatures applying the method of Green functions. The renormalized phonon frequencies for different temperatures are presented in two cases. In the first case the interaction between TTT chains is neglected. In the second one, this interaction is taken into account. Computer simulations for the 3D physical model of the TTT<sub>2</sub>I<sub>3</sub> crystal are performed for different values of dimensionless Fermi momentum <em>k</em><sub>F</sub>, that is determined by variation of carrier concentration. It is shown that the transition is of Peierls type and strongly depends on iodine concentration. Finally, the Peierls critical temperature was determined.展开更多
基金financially supported by the National Natural Science Foundation of China(No.52103029)。
文摘Polyimide(PI)is widely used in high-frequency communication technology due to its exceptional comprehensive properties.However,traditional PI has a relatively elevated dielectric constant and dielectric loss.Herein,the different cross-linked structures were introduced in PI matrix and conducted a detailed discussion on the influence of cross-linking agent content and cross-linking structure type on the overall performance of PI films.In comparison to the dielectric constant of 2.9 of neat PI,PI with an interchain cross-linking structure containing 2 wt%1,3,5-tris(4-aminophenyl)benzene(TAPB)(interchain-PI-2)exhibited the reduced dielectric constant of 2.55 at 1 MHz.The PI films with intrachain crosslinking structure containing 2 wt%TAPB(intrachain-PI-2)exhibited the lowest dielectric constant of 2.35 and the minimum dielectric loss of0.0075 at 1 MHz.It was due to the more entanglement junctions of intrachain-PI resulting in decreased carrier transport.The thermal expansion coefficients of both interchain-PI and intrachain-PI films were effectively reduced.Moreover,in contrast to interchain-PI films,the intrachain-PI films maintained colorlessness and transparency as the cross-linking agent content increased.This work compared the effects of two different cross-linked structures on the performance of PI films and provided a feasible way to obtain low-k PI films with excellent comprehensive performance for 5G applications.
基金supported by the National Research Foundation of Korea(NRF)grants funded by the Korea government(MSIT)(2022R1F1A1065586,2019R1A6A1A11053838)the GIST Research Institute(GRI)APRI grant funded by the GIST in 2022.
文摘Bulk heterojunction(BHJ)composites show improved power conversion efficiencies when optimized in terms of morphology using various film processing methods.A reduced carrier recombination loss in an optimized BHJ was characterized previously.However,the driving force that leads to this reduction was not clearly understood.In this study,we focus on the decreased carrier recombination loss and its driving force in optimized nonfullerene acceptor-based PTB7-Th:IEICO-4F BHJ composites.We demonstrate that the optimized BHJ shows deactivation in the sub-nanosecond nongeminate carrier recombination process.The driving force for this deactivation was determined to be the improved interchain hole delocalization between the polymers.An enhanced interchain hole delocalization was observed using steady-state photoinduced absorption(PIA)spectroscopy.In particular,increased splitting between the polaron PIA bands was noted.Moreover,improved interchain hole delocalization was observed for other state-of-the-art BHJ materials,including D18:Y6 with optimized morphologies.
基金supported by the National Natural Science Foundation of China(Grant Nos.12175315 and 12205385)。
文摘We propose a novel approach to generate and manipulate topological Floquet bound states in the continuum(BICs)via a class of systems constructed by coupling two identical periodically driven one-dimensional Su-Schrieffer-Heeger chains.The formation of topological Floquet BICs can be adjusted only by tuning the driving amplitude or frequency,regardless of whether the static system has BICs or not.The interchain bias can only change the localization property of topological Floquet BICs,and a bigger bias can lead to transforming topological Floquet BICs into bound states out of the continuum(BOCs).But it does not change the topological properties of these topological Floquet states.Based on the repulsion effect of edge states,we propose to detect occurrence of topological Floquet BICs and transition point between topological Floquet BICs and BOCs using quantum walk.Our work provided a convenient and realistic approach for the experimental realization and manipulation of BICs in a single-particle quantum system.
文摘Polaron dynamics in a system of highly ordered conjugated polymer chains is investigated based on the tight binding model. With the interchain coupling enhancing,it takes longer time for the electron added to the system to induce a localized polaron state. Beyond a certain strength of the interchain coupling,the electron evolves into a two-dimensional delocalized polaron state. Dynamical simulations suggest that the well-ordered organic molecule systems with two-dimensional polarons exhibit higher mobilities than the systems with intrachain localized polarons,as also suggested by earlier experiments.
文摘The photoluminescence(PL) properties of poly[ (2, 5 - diphenylene - 1, 3, 4 - oxadiazole) - 4, 4’ - viny-lene] (O - PPV) are investigated using absorption and excitation measurements for different concentration ratios of solid-state O - PPV/ PEO (polyethylene oxide ) blends, as well as by comparing PL spectra for dilute solution and solid state pristine O - PPV. The solid film of O - PPV/PEO is prepared to investigate the interaction between polymers. The O - PPV molecules are dispersed into PEO which is used as a inert material in order to change the interaction between O - PPV. In the O -PPV/PEO blends, it is found that the PL spectra excited by 300nm for different concentration ratios are different. There are three peaks in the PL spectra of 1: 100 and 1: 200 (O - PPV/PEO) blends, and the relative intensities of peaks at 500nm and 460nm gradually decrease with lowering the concentrations of O - PPV. There leaves one peak at 416nm when the ratio of O - PPV to PEO is below 1: 300, and PL shape does not change any longer. The results show that the solid-state O - PPV emission arises from interchain charge-transfer states due to interchain effects.According to the absorption and photoluminescence spectra of the solid films, it is also believed that there are types of localized and delocalized states in conjugated polymers. The two types of states have different effects on charge-transfer state in different concentrations of solid films.
基金Supported by National Natural Science Foundation of China (No.30970724)Natural Science Foundation of Tianjin (No.08JCYBJC03400)
文摘Type Ⅰ Ⅲ and Ⅴ collagens were extracted from bovine dermis and cornea by using pepsin treatment in acetic acid solution, followed by salt precipitation and dialysis, to purify and isolate each type of collagens. The preparation process was analyzed by using sodium dodecyl sulfate polyacrylamide gel electrophoresis （SDS-PAGE）. A reducing agent, 2-mercaptoethanol, was used to remove disulfide bonds and analyze the structure of the bonds involved between α chains in some types of collagens. The use of delayed reducing methods resulted in the difference between α1 （Ⅲ） and α1 （ Ⅰ ） chains in a mixture containing type Ⅰ and Ⅲ collagens. The structure of disulfide bonds among α chains exists potentially in type V collagen prepared from the pepsin-treatment extraction at 4 ℃, which differs from type Ⅲ collagen in relation to the locations of disulfide bonds. Compared with pepsin-treated collagen at 4 ℃, the relative molecular weights of α1 （V） and α2 （V） chains treated at room temperature decrease by 4.6% and 6.0%, respectively. It is concluded that type Ⅰ Ⅲ and Ⅴ collagens can be prepared from bovine dermis and cornea by the use of pepsin treatment, salt precipitation and dialysis. The interchain disulfide bonds lie potentially near the edges of termini of type V collagen molecules in extracellular matrix, and a small number of interchain crosslinks exist in type V collagen.
文摘The Peierls structural transition in quasi-one-dimensional organic crystals of TTF-TCNQ is investigated in the frame of a more complete physical model. The two most important electron-phonon interaction mechanisms are taken into account simultaneously. One is similar of that of deformation potential and the other is of polaron type. For simplicity, the 2D crystal model is considered. The renormalized phonon spectrum and the phonon polarization operator are calculated in the random phase approximation for different temperatures. The effects of interchain interaction on renormalized acoustic phonons and on the Peierls critical temperature are analyzed.
文摘We investigate the metal-insulator transition in quasi-one-dimensional organic crystals of tetrathiotetracene-iodide, TTT2I3, in the 2D model. A crystal physical model is applied which takes into account two the most important hole-phonon interaction mechanisms. One is similar to that of deformation potential and the other is of polaron type. The scattering on defects is also considered and it is crucial for the explanation of the transition. The phonon polarization operator and the renormalized phonon spectrum are calculated in the random phase approximation for different temperatures applying the method of Green functions. We show that the transition is of Peierls type. The effect of lattice distortion on the dispersion of renormalized acoustic phonons is analyzed.
文摘The Peierls structural transition in the TTT<sub>2</sub>I<sub>3</sub> (tetrathiotetracene-iodide) crystal, for different values of carrier concentration is studied in 3D approximation. A crystal physical model is applied that considers two of the most important hole-phonon interactions. The first interaction describes the deformation potential and the second one is of polaron type. In the presented physical model, the interaction of carriers with the structural defects is taken into account. This is crucial for the explanation of the transition. The renormalized phonon spectrum is calculated in the random phase approximation for different temperatures applying the method of Green functions. The renormalized phonon frequencies for different temperatures are presented in two cases. In the first case the interaction between TTT chains is neglected. In the second one, this interaction is taken into account. Computer simulations for the 3D physical model of the TTT<sub>2</sub>I<sub>3</sub> crystal are performed for different values of dimensionless Fermi momentum <em>k</em><sub>F</sub>, that is determined by variation of carrier concentration. It is shown that the transition is of Peierls type and strongly depends on iodine concentration. Finally, the Peierls critical temperature was determined.
