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1.
Five new thermally robust electroluminescent fluorene‐based conjugated copolymers, including poly[2,7‐(9,9‐dioctylfluorene)‐co‐4,7‐{5,6‐bis(3,7‐dimethyloctyloxymethyl)‐2,1,3‐(benzothiadiazole)}] ( PFO‐P2C10BT ) were synthesized and used to fabricate the efficient polymer light‐emitting diodes (PLEDs). The glass transition temperatures of the polymers were found to be higher than that of poly(9,9‐dialkylfluorenes) and are in the range 113–165 °C. We fabricated PLEDs in indium‐tin oxide/PEDOT/light‐emitting polymer/cathode configurations using either double‐layer LiF/Al or triple‐layer Alq3/LiF/Al cathode structures. The new copolymers were found to have emission colors that vary from greenish blue (491 nm) to green (543 nm) depending on the copolymer composition. The maximum brightness and luminance efficiency of these PLEDs were found to be up to 5347 cd/m2 and 1.51 cd/A at 10 V, respectively. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6762–6769, 2008  相似文献   

2.
A novel phenothiazine‐based polymer was synthesized through the Heck reaction of 3,7‐divinyl‐N‐octyl‐phenothiazine with 4,7‐dibromo‐2‐octylbenzotriazole according to the alternating donor–acceptor strategy. The polymer was characterized with 1H NMR, infrared spectroscopy, gel permeation chromatography, cyclic voltammetry, ultraviolet–visible spectroscopy, and fluorescence spectroscopy. With the polymer used as an active layer, three nondoped polymer light‐emitting diodes (PLEDs) with a double‐layer configuration were fabricated by the spin‐coating approach with different thermal annealing processes. The emission maximum in electroluminescent spectra was stabilized at 616 nm. The maximum luminance reached 2432 cd/m2. The coordinate value of Commission International de l'Eclairage 1931 in the double‐layer PLEDs after the thermal treatment was nearly stabilized at (x, y) =(0.62, 0.38). Additionally, the luminous efficiency of device II reached a balanceable state with an increase in the current. Therefore, the polymer had an orange‐red emission with stable chromaticity coordinates under different driving voltages. Finally, a nondoped device with a stable luminous efficiency and chromaticity was obtained. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4867–4878, 2007  相似文献   

3.
Tri(pyrazolyl)phosphanes ( 5 R1,R2) are utilized as an alternative, cheap and low‐toxic phosphorus source for the convenient synthesis of InP/ZnS quantum dots (QDs). From these precursors, remarkably long‐term stable stock solutions (>6 months) of P(OLA)3 (OLAH=oleylamine) are generated from which the respective pyrazoles are conveniently recovered. P(OLA)3 acts simultaneously as phosphorus source and reducing agent in the synthesis of highly emitting InP/ZnS core/shell QDs. These QDs are characterized by a spectral range between 530–620 nm and photoluminescence quantum yields (PL QYs) between 51–62 %. A proof‐of‐concept white light‐emitting diode (LED) applying the InP/ZnS QDs as a color‐conversion layer was built to demonstrate their applicability and processibility.  相似文献   

4.
A new series of sulfide‐substituted poly(1,4‐phenylene vinylene) derivatives ( S1PPV–S3PPV ) with different composition ratios were successfully synthesized via the Gilch route. The CdSe/ZnS were grafted to the sulfur atoms by ligand exchange reaction. The grafted CdSe/ZnS contents were determined from TGA analysis to be from 4.6 to 37.8%. A new peak at 1151 cm?1 formed in FT‐IR after ligand exchange, which is attributed to the force formation between sulfur and CdSe. The GPC results show that the molecular weights of final polymers became higher after ligand exchange. Thin films of obtained polymers emitted bright green and yellow light with the max emission peak located from 546 to 556 nm. Double‐layer LEDs with an ITO/PEDOT/polymer/Ca/Al configuration were fabricated to evaluate the potential use of these polymers. The turn‐on voltages of the devices were about 4–5 V. As the CdSe/ZnS content increased in grafted polymers, the device performance was significantly enhanced as compared to pristine polymers. In the case of S3PPV , the double‐layer device showed a maximum luminance of 6073 cd/m2 with a current yield of 0.82 cd/A. The maximum luminance and current yield was enhanced to 13,390 cd/m2 and 2.25 cd/A by grafting CdSe/ZnS onto polymers. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5378–5390, 2006  相似文献   

5.
Carrier balance is essential to obtain efficient emission in polymer light‐emitting diodes (PLEDs). A new polymer 3P5O composed of alternating p‐terphenyl and tetraethylene glycol ether segments is designed and synthesized by the Suzuki coupling reaction and successfully employed as hole‐buffer layer to improve carrier balance. Multilayer PLEDs [ITO/PEDOT:PSS/ 3P5O /SY/LiF/Al], with Super Yellow (SY) as the emitting layer and 3P5O as the hole‐buffer layer, reveal maximum luminance (17,050 cd/m2) and maximum current efficiency (6.6 cd/A) superior to that without the hole‐buffer layer (10,017 cd/m2, 3.0 cd/A). Moreover, it also shows better performance than that using conventional BCP as hole‐blocking layer [ITO/PEDOT:PSS/SY/BCP/LiF/Al (80 nm): 13,639 cd/m2, 4.1 cd/A]. The performance enhancement has been attributed to hole‐buffering characteristics of 3P5O that results in improved carrier recombination ratio and wider carrier recombination region. Current results indicate that the 3P5O is a promising hole‐buffer polymer to enhance the performance of optoelectronic devices. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 785–794  相似文献   

6.
Novel photo‐crosslinkable hole‐transport and host materials incorporated into multilayer blue phosphorescent polymer light‐emitting diodes (Ph‐PLEDs) were demonstrated in this study. The oxetane‐containing copolymers, which function as hole‐transport layers (HTL), could be cured by UV irradiation in the presence of a cationic photoinitiator. The composition of the two monomers was varied to yield three different hole‐transporting copolymers, [Poly(9,9′‐(5‐(((4‐(7‐(4‐(((3‐methyloxetan‐3‐yl)methoxy)methyl)phenyl)octan‐3‐yl)benzyl)oxy)methyl)?1,3‐phenylene)bis(9H‐carbazole)) ( P(mCP‐Ox)‐I , ‐II , and ‐III )]. In addition, monomer 1 was copolymerized with styrene to produce copolymer P(mCP‐Ph) as a host material for bis[2‐(4,6‐difluorophenyl)pyridinato‐C2,N](picolinato)iridium(III) (FIrpic), a blue‐emitting dopant. All mCP‐based copolymers displayed high glass transition temperatures (Tg) of up to 130–140 °C and triplet energies of up to 3.00 eV. The blue Ph‐PLEDs exhibited a maximum external quantum efficiency of 2.55%, in addition to a luminous efficiency of 8.75 cd A?1 when using the device configuration of indium tin oxide/poly(3,4‐ethylenedioxythiophene):poly(styrene sulfonate)/ P(mCP‐OX)‐III / P(mCP‐Ph) :FIrpic(15 wt %)/3,3′‐[5′‐[3‐(3‐pyridinyl)phenyl][1,1′:3′,1′′‐terphenyl]‐3,3′′‐diyl]bispyridine/LiF/Al. The device bearing P(mCP‐Ox)‐III HTL, containing the highest composition of mCP unit, exhibited better performance than the other devices, which is attributed to induction of more balanced charge carriers and carrier recombination in the emissive layer. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 707–718  相似文献   

7.
Deep blue emitting copolymers were synthesized by uniting the Eumelanin‐inspired indole core with fluorene and carbazole units via Suzuki polymerization. The resulting polymers, PIF and PIC, showed deep blue emission in the range of 416–418 nm and quantum yields of 0.39–0.60. Both polymers exhibited an intense and stable electrogenerated chemiluminescence. Interestingly, deep HOMO levels of −5.71 and −5.61 eV were observed for PIF and PIC, respectively. Solution processed polymer light emitting diodes (PLEDs) were fabricated using the PIF as a guest. PLEDs emitted deep blue light at 418 nm, with the luminous efficiency peaking at 1 Cd/A, given that the photopic response at that wavelength is 0.0151. The electroluminescence of PIF displayed a Commission Internationale de l'Eclairage coordinates of (0.16, 0.07) with a maximum external quantum efficiency of 1.1%. Hence, these materials prove to be promising candidates for the fabrication of deep blue PLEDs. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2018 , 56, 125–131  相似文献   

8.
A series of random copolymers POC10{Poly(2,5‐bis[(5‐decyloxy‐phenyl)‐1,3,4‐oxadiazole]styrene)}‐co‐Poly(N‐vinylcarbazole) (PVK) with different nvk content were synthesized through common radical polymerization and were incorporated into light emitting diodes as emitting layers. The structures and properties of the copolymers were characterized and evaluated by GPC, TGA, DSC, UV, PL, CV, and EL analyses. All the polymers enjoy high thermal stability. Cyclic voltammetry revealed that, with the incorporation of N‐vinylcarbazole to the copolymer, these copolymers had high‐lying HOMO energy values, which facilitated hole injection. PL peaks in the film show blue‐shift compared with those in solutions and fluorescent quantum efficiency decreased with the nvk content increasing, which supported the efficient energy transfer from nvk units to the oxadiazole units. Single‐layer LEDs with the configuration of ITO/PEDOT/PC10‐nvk/Mg:Ag/Ag were fabricated, which emit a blue light around 440 and 490 nm with a maximum brightness of 675.3 cd/m2 and luminous efficiency of 0.108 cd/A. Moreover, we fabricated electrophosphorescent device from bipolar transport copolymer PC10‐nvk4 as host material and an orange‐light‐emitting iridium phosphor IrMDPP as guest. The maximum luminous efficiency of 0.548 cd/A was obtained. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 5452–5460, 2008  相似文献   

9.
The key to utilizing quantum dots (QDs) as lasing media is to effectively reduce non‐radiative processes, such as Auger recombination and surface trapping. A robust strategy to craft a set of CdSe/Cd1?xZnxSe1?ySy/ZnS core/graded shell–shell QDs with suppressed re‐absorption, reduced Auger recombination rate, and tunable Stokes shift is presented. In sharp contrast to conventional CdSe/ZnS QDs, which have a large energy level mismatch between CdSe and ZnS and thus show strong re‐absorption and a constrained Stokes shift, the as‐synthesized CdSe/Cd1?xZnxSe1?ySy/ZnS QDs exhibited the suppressed re‐absorption of CdSe core and tunable Stokes shift as a direct consequence of the delocalization of the electron wavefunction over the entire QD. Such Stokes shift‐engineered QDs with suppressed re‐absorption may represent an important class of building blocks for use in lasers, light emitting diodes, solar concentrators, and parity‐time symmetry materials and devices.  相似文献   

10.
A new design for a quasi‐solid‐state Forster resonance energy transfer (FRET) enabled solar cell with unattached Lucifer yellow (LY) dye molecules as donors and CdS/CdSe quantum dots (QDs) tethered to titania (TiO2) as acceptors is presented. The Forster radius is experimentally determined to be 5.29 nm. Sequential energy transfer from the LY dye to the QDs and electron transfer from the QDs to TiO2 is followed by fluorescence quenching and electron lifetime studies. Cells with a donor–acceptor architecture (TiO2/CdS/CdSe/ZnS‐LY/S2?‐multi‐walled carbon nanotubes) show a maximum incident photon‐to‐current conversion efficiency of 53 % at 530 nm. This is the highest efficiency among Ru‐dye free FRET‐enabled quantum dot solar cells (QDSCs), and is much higher than the donor or acceptor‐only cells. The FRET‐enhanced solar cell performance over the majority of the visible spectrum paves the way to harnessing the untapped potential of the LY dye as an energy relay fluorophore for the entire gamut of dye sensitized, organic, or hybrid solar cells.  相似文献   

11.
A series of white polymer light emitting displays (PLEDs) based on a polymer blend of polyalkylfluorenes and poly(2‐methoxy‐5,2′‐ethyl‐hexyloxy‐1,4‐phenylene vinylene) (MEH‐PPV) was developed. MEH‐PPV or red light emitting alkyfluorene copolymer (PFR) was blended with blue light emitting alkyfluorene copolymer (PFB), and MEH‐PPV was blended with both green light emitting alkyfluorene copolymer (PFG) and PFB to generate white light emission PLEDs. Low turn on voltage (2.7 V), high brightness (12,149 nits), high efficiency (4.0 cd/A, 4.0 lm/W), and good color purity (Commission Internationale de L'Eclairage (CIEx,y) co‐ordinates (0.32, 0.34)) were obtained for the white PLEDs based on the PFB and MEH‐PPV polymer blend. Exciplex formation in the interface between PFR and PFB induced a new green emission peak for these two components based white PLEDs. As a result, strong white emission (4078 nits) was obtained by mixing the red, green, and blue (RGB) three primary colors. High color purity of blue (CIE, x = 0.14, y = 0.08), green (CIE, x = 0.32, y = 0.64) and red (CIE, x = 0.67, y = 0.33) emissions was achieved for white PLEDs combining with dielectric interference color‐filters. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 330–341, 2007  相似文献   

12.
A new series of copolymers with high brightness and luminance efficiency were synthesized using the Gilch polymerization method, and their electro‐optical properties were investigated. The weight‐average molecular weights (Mw) and polydispersities of the synthesized poly(9,9‐dioctylfluorenyl‐2,7‐vinylene) [poly(FV)], poly[2‐(3‐dimethyldodecylsilylphenyl)‐1,4‐phenylenevinylene] [poly(m‐SiPhPV)], and poly[9,9‐di‐n‐octylfluorenyl‐2,7‐vinylene]‐co‐(2‐(3‐dimethyldodecylsilylphenyl)‐1,4‐phenylene vinylene)] [poly(FV‐com‐SiPhPV)] were found to be in the ranges of (8.7–32.6) × 104 and 2.3–5.4, respectively. It was found that the electro‐optical properties of the copolymers could be adjusted by controlling the feed ratios of the comonomers. Thin films of poly(FV), poly(m‐SiPhPV), and poly(FV‐com‐SiPhPV) were found to exhibit photoluminescence quantum yields between 21% and 42%, which are higher than those of MEH‐PPV. Light‐emitting diodes were fabricated in ITO/PEDOT/light‐emitting polymer/cathode configurations using either double layer (LiF/Al) or triple layer (Alq3/LiF/Al) cathode structures. The performance of the polymer light‐emitting diodes (PLEDs) with triple layer cathodes was found to be better than that of the PLEDs with double layer cathodes in poly(FV) and poly(FV‐com‐SiPhPV). The turn‐on voltages of the PLEDs were in the range of 4.5–6.0 V, with maximum brightness and luminance efficiency up to 9691 cd/m2 at 16 V and 3.27 cd/A at 13 V, respectively. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 5062–5071, 2005  相似文献   

13.
A blue fluorescent polymer based on poly(vinyl carbazole) (PVK) and terfluorene, combined to make a chemical hybrid at the carbazole unit (PVK‐TF), is fully characterized in this study. PVK‐TF shows useful emission features, such as peaks at 400, 420, 437, 460, and 496 nm, depending on the processing conditions. It possesses a relatively high triplet energy level (2.23 eV), electrochemical stability, good film‐forming ability, and morphological stability. Based on this blue fluorescent material, highly efficient orange phosphorescent polymer light‐emitting diodes (PLEDs) were fabricated with a maximum efficiency of 21.99 cd A?1, and a maximum luminance of 19552.3 cd m?2. Single‐layer hybrid white PLEDs were developed, with a high color rendering index of 81.9 that emitted across the whole visible spectrum from 380 to 780 nm, corresponding to the Commission International de L'Eclairage coordinates x, y values of around (0.38, 0.40) and CCT = 3774, with a maximum current efficiency of 10.69 cd A?1, and a maximum brightness of 15723.3 cd m?2. © 2014 Wiley Periodicals, Inc. J. Polym. Sci. Part B: Polym. Phys. 2014 , 52, 587–595  相似文献   

14.
Nonconjugated bipolar transport polymers have been developed as host materials for electroluminescent devices by incorporating both electron‐transporting and hole‐transporting functionalities into copolymers. The random copolymer PCt‐nvk3‐7 containing mesogen‐jacketed segment of P‐Ct have been synthesized and characterized. The effect of mesogen‐jacketed segment content of these bipolar copolymers on device performance has been investigated. The results of polymer light‐emitting diodes (PLEDs) show that the jacketed content of copolymers has a significant effect on device performance: lowering charge transport and facilitating the hole‐electron recombination leads to much higher current efficiency. Applying these high triplet random copolymers as host, the maximum current efficiency of 0.70 cd/A and the maximum brightness of 1872.8 cd/m2 was achieved for PCt‐nvk3‐7 with an orange‐emitting complex dopant. The results suggest that the bipolar copolymers PCt‐nvks can be good host polymers for electrophosphorescent devices. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7861–7867, 2008  相似文献   

15.
A novel blue‐emitting polymer based on 3,6‐silafluorene and 2,7‐silafluorene was synthesized via the Suzuki polycondensation. The resulting polymers are readily soluble in common organic solvents, such as toluene, xylene, THF, and chloroform. The thermal, electrochemical, photophysical, and electroluminescence properties of the resulting polymers were investigated. The device fabricated from the copolymer with a configuration of ITO/PEDOT:PSS/PVK/polymer/Ba/Al exhibited an external quantum efficiency of 1.95%, a luminous efficiency of 1.69 cd A?1 and a maximal brightness of 6000 cd m?2. It has been found that the incorporation of the 3,6‐silafluorene unit into the poly(2,7‐silafluorene) main chain can not only improve the color purity of the devices from the resulting copolymer but also enhance its device efficiency. Moreover, no undesired long‐wavelength green emission was observed in the PL spectra of P36‐27SiF90 compared to that of PFO with a dominating emission at 500–600 nm after thermal annealing at 200 °C for 8 h. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 4941–4949, 2007  相似文献   

16.
A hole‐injection/transport bilayer structure on an indium tin oxide (ITO) layer was fabricated using two photocrosslinkable polymers with different molecular energy levels. Two photoreactive polymers were synthesized using 2,7‐(or 3,6‐)‐dibromo‐9‐(6‐((3‐methyloxetan‐3‐yl)methoxy)hexyl)‐9H‐carbazole) and 2,4‐dimethyl‐N,N‐bis(4‐ (4,4,5,5‐tetramethyl‐1,3,2‐dioxaborolan‐2‐yl)phenyl)aniline via a Suzuki coupling reaction. When the oxetane groups were photopolymerized in the presence of a cationic photoinitiator, the photocured film showed good solvent resistance and compatibility with a poly(N‐vinylcarbazole) (PVK)‐based emitting layer. Without the use of a conventional hole injection layer (HIL) of poly(3,4‐ethylenedioxythiophene)/(polystyrenesulfonate) (PEDOT:PSS), the resulting green light‐emitting device bearing PVK: 5‐4‐tert‐butylphenyl‐1,3,4‐oxadiazole (PBD):Ir(Cz‐ppy)3 exhibited a maximum external quantum efficiency of 9.69%; this corresponds to a luminous efficiency of 29.57 cd/A for the device K‐4 configuration ITO/POx‐I/POx‐II/PVK:PBD:Ir(Cz‐ppy)3/triazole/Alq3/LiF/Al. These values are much higher than those of PLEDs using conventional PEDOT:PSS as a single HIL. The significant improvement in device efficiency is the result of suppression of the hole injection/transport properties through double‐layered photocrosslinked‐conjugated polymers. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012  相似文献   

17.
以3-巯基丙酸作为修饰剂,在水溶液中合成了稳定的CdSe/ZnS量子点(QDs),透射电镜观察所合成量子点的形貌近似球形,粒径约为25 nm.吸收光谱与荧光光谱的研究表明,CdSe QDs在410 nm处有最大吸收峰,而CdSe/ZnS QDs的最大吸收峰在470 nm处,CdSe/ZnS QDs的荧光强度是CdSe QDs的11倍.考察了缓冲溶液的体积、pH值、反应温度、反应时间对体系荧光的影响.在最佳实验条件下,体系的荧光强度与BSA的浓度呈线性关系,线性响应范围为0.746×10-7~4.48×10-7 mol/L,检出限为3.846×10-10 mol/L.并且CdSe/ZnS QDs荧光强度基本保持稳定,可达两个多月.该方法应用于合成样品的测定,结果满意.  相似文献   

18.
A series of novel arylene ether polymers (P5F‐BCzVFs) containing both pentafluorene (5F) and distyrylarylene derivative (BCzVF) units in the side chains for efficient pure blue light emission were prepared by a facile, metal‐free condensation polymerization. The emission spectra indicated that color tuning could be achieved through efficient Förster energy transfer from the deep‐blue 5F host to the pure‐blue BCzVF dopant. Single‐layer polymer light‐emitting diodes (PLEDs) based on P5F‐BCzVFs (ITO/(PEDOT:PSS)/polymer/Ca/Al) exhibited voltage‐independent and stable pure blue emission with a Commission International de L'Eclairage (CIE) coordinate of (0.15, 0.15), a maximum brightness of 3576 cd/m2, and a maximum luminous efficiencies of 2.15 cd/A, respectively. As most polymers with dopant‐host systems, the luminous efficiencies of all P5F‐BCzVFs surpassed that of the host‐only polymer (P5F), due to the energy transfer and charge trapping from the host to the dopant. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011  相似文献   

19.
A series of novel styrene derived monomers with triphenylamine‐based units, and their polymers have been synthesized and compared with the well‐known structure of polymer of N,N′‐bis(3‐methylphenyl)‐N,N′‐diphenylbenzidine with respect to their hole‐transporting behavior in phosphorescent polymer light‐emitting diodes (PLEDs). A vinyltriphenylamine structure was selected as a basic unit, functionalized at the para positions with the following side groups: diphenylamine, 3‐methylphenyl‐aniline, 1‐ and 2‐naphthylamine, carbazole, and phenothiazine. The polymers are used in PLEDs as host polymers for blend systems with the following device configuration: glass/indium–tin–oxide/PEDOT:PSS/polymer‐blend/CsF/Ca/Ag. In addition to the hole‐transporting host polymer, the polymer blend includes a phosphorescent dopant [Ir(Me‐ppy)3] and an electron‐transporting molecule (2‐(4‐biphenyl)‐5‐(4‐tert‐butylphenyl)‐1,3,4‐oxadiazole). We demonstrate that two polymers are excellent hole‐transporting matrix materials for these blend systems because of their good overall electroluminescent performances and their comparatively high glass transition temperatures. For the carbazole‐substituted polymer (Tg = 246 °C), a luminous efficiency of 35 cd A?1 and a brightness of 6700 cd m?2 at 10 V is accessible. The phenothiazine‐functionalized polymer (Tg = 220 °C) shows nearly the same outstanding PLED behavior. Hence, both these polymers outperform the well‐known polymer of N,N′‐bis(3‐methylphenyl)‐N,N′‐diphenylbenzidine, showing only a luminous efficiency of 7.9 cd A?1 and a brightness of 2500 cd m?2 (10 V). © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3417–3430, 2010  相似文献   

20.
Imaging pancreatic cancer using surface-functionalized quantum dots   总被引:1,自引:0,他引:1  
In this study, CdSe/CdS/ZnS quantum dots (QDs) were used as optical contrast agent for imaging pancreatic cancer cells in vitro using transferrin and anti-Claudin-4 as targeting ligands. CdSe/CdS/ZnS was chosen because the CdSe/CdS/ZnS QDs have better photoluminescence (PL) efficiency and stability than those of CdSe/ZnS. The transferrin-mediated targeting is demonstrated in both a cell-free coprecipitation assay as well as using in vitro confocal microscopy. Pancreatic cancer specific uptake is also demonstrated using the monoclonal antibody anti-Claudin-4. This targeted QD platform will be further modified for the purpose of developing as an early detection imaging tool for pancreatic cancer.  相似文献   

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