融合聚光导光与双模辅助的智能照明系统

智能照明是近年来新兴的行业,具有节能环保、舒适健康、智能便捷等特点。智能照明利用智能控制技术和计算机技术对照明系统进行监控、调节和管理,以满足人们在不同环境条件下的照明需求。随着LED照明系统向智能化方向发展,融合聚光导光与双模辅助的智能照明系统应运而生,并逐渐在照明领域得到应用。以聚光导光技术为基础,通过导光材料和导光技术实现对室外照明光线的高效利用,为室内外照明提供一种绿色健康的照明方式,不仅能有效解决传统照明系统所带来的光污染、眩光等问题,而且能通过双模控制技术实现对照明区域的智能分区控制,从而提高公共空间照明系统的舒适性和安全性。

Aggregation-Induced Emission with Large Redshift in 2,7-Diphenylfluorenone:Reality or Artifact?

The luminescence property of 2,7-diphenyl-fluorenone(DPFO)was previously reported to be very unusual with a large aggregationinduced effect associated with a fluorescence redshift of 150 nm.The phenomenon is reexamined in this work.It is found that the abnormal observations are caused by the presence of a trace amount of impurity 2,7-diphenyl-fluorene(DPF)in the as-synthesized DPFO.The pure DPFO molecule does have an intense fluorescence(FL)in solid(528 nm),about 4−5 times larger than in its dilute dichloromethane solutions(542 nm),but with a blueshifted rather than redshifted FL wavelength in solid.The enormous FL enhancement and redshifted FL wavelength of the as-synthesized DPFO solid are due to the presence of impurity DPF.The FL of DPF is much stronger than that of DPFO in dilute solutions and it also has shorter FL wavelengths.In a dilute solution of DPFO with a trace amount of DPF(∼1%),the dominant FL peaks are from DPF.Because the electronic absorption peaks of DPF overlaps with DPFO,the electronic energy of DPF can transfer to DPFO.The energy transfer is faster with the increase of concentration because DPF and surrounding DPFO molecules become closer,which quenches the FL of DPF(356 and 372 nm)and enhances the FL of DPFO(542 nm in solution and 528 nm in solid).Therefore,at high concentrations or in solids,only peak at about 542 or 528 nm shows up,and peaks at 356 and 372 nm disappear.

Effects of Intermolecular Interactions on Luminescence Property in Organic Molecules

The organic solid-state lightemitting materials have attracted more and more attention owing to their promising applications in displays,lasers and optical communications.In contrast to isolated molecule,there are various weak intermolecular interactions in organic solids that sometimes have a large impact on the excited-state properties and energy dissipation pathways,resulting in strong fluorescence/phosphorescence.It is increasingly necessary to reveal the luminescence mechanism of organic solids.Here,we briefly review how intermolecular interactions induce strong normal fluorescence,thermally activate delayed fluorescence and room-temperature phosphorescence in organic solids by examining changes in geometry,electronic structures,electron-vibration coupling and energy dissipation dynamics of the excited states from isolated to aggregated molecules.We hope that the review will contribute to an in-depth understanding of the excited state properties of organic solids and to the design of excellent solid-state light-emitting materials.

Loss Measurements on Polymer Thin Film Optical Waveguides

A simple setup for the measurement of transmission loss in polymer thin film optical waveguides is described. A new electro-optic polymer film has been prepared. The transmission loss of the film is measured before and after corona poling. And the loss is determined to be 1.84 dB/cm and 2.14 dB/cm, respectively.

New Insights into Folding Kinetics of α,ω Dye-Functionalized Poly(N-isopropylacrylamide)

Two narrowly-distributed poly(N-isopropylacrylamide)(PNIPAM) samples were prepared via atom transfer radical polymerization (ATRP) with a novel dansyl functionalized initiator. The other end of the PNIPAM was functionalized by dabcyl group via click reaction. From the static fluorescence measurements, the fluorescence intensity of dansyl group and energy transfer efficiency between dansyl and dabcyl groups increased when the temperature increased from 36 °C to 45 °C, indicating that the microenvironment surrounding dansyl became hydrophobic and the distance between dansyl and dabcyl decreased. The kinetics of the conformational change of the dye-labeled PNIPAM was studied by a home-made laser-induced temperature jump device with fluorescent measurement. Our results revealed that the characteristic transition time was 3.8 and 5.8 ms for PNIPAM with degrees of polymerization of 85 and 142, respectively, indicating that the characteristic transition time was related to the chain length. Besides, characteristic transition time for the change of the energy transfer efficiency was 2.9 ms for PNIPAM with the degree of polymerization of 85, suggesting that the energy transfer efficiency change was faster than the fluorescence intensity change of dansyl group.

Construction of Type I Aggregation-Induced Emission Photosensitizers for Photodynamic Therapy via Photoinduced Electron Transfer Mechanism

Photodynamic therapy(PDT)as a non-invasive anticancer modality has received increasing attention due to its advantages of noninvasiveness,high temporospatial selectivity,simple and controllable operation,etc.PDT mainly relies on the generation of toxic reactive oxygen species(ROS)by photosensitizers(PSs)under the light irradiation to cause cancer cell apoptosis and death.However,solid tumors usually exhibit an inherent hypoxic microenvironment,which greatly limits the PDT efficacy of these high oxygen-dependent conventional type II PSs.Therefore,it is of great importance to design and develop efficient type I PSs that are less oxygen-dependent for the treatment of hypoxic tumors.Herein,a new strategy for the preparation of efficient type I PSs by introducing the photoinduced electron transfer(PET)mechanism is reported.DR-NO_(2) is obtained by introducing 4-nitrobenzyl to(Z)-2-(5-(4-(diethylamino)-2-hydroxybenzylidene)-4-oxo-3-phenylthiazolidin-2-ylidene)malononitrile(DR-OH)with aggregation-induced emission(AIE)feature.The AIE feature ensures their high ROS generation efficiency in aggregate,and the PET process leads to fluorescence quenching of DR-NO_(2) to promote triplet state formation,which also promotes intramolecular charge separation and electron transfer that is conducive for type I ROS particularly superoxide radicals generation.In addition,DR-NO_(2) nanoparticles are prepared by nanoprecipitation to possess nanoscaled sizes,high cancer cell uptake,and excellent type I ROS generation ability,which results in an excellent performance in PDT ablation of MCF-7 cancer cells.This PET strategy for the development of type I PSs possesses great potential for PDT applications against hypoxic tumors.

Self-assembled nanostructured photosensitizer with aggregation-induced emission for enhanced photodynamic anticancer therapy

Three nanostructured photosensitizers with aggregation-induced emission(AIE) characteristics based on2,3-bis(4?-(diphenylamino)-[1,1?-biphenyl]-4-yl) fumaronitrile(BDBF) were prepared for image-guided photodynamic therapy(PDT). BDBF was encapsulated with Pluronic F-127(F127) to form usual spherical nanoparticles(F127@BDBF NPs) with a red fluorescence emission and 9.8% fluorescence quantum yield(FQY). Moreover, BDBF self-assembled into nanorods(BDBF NRs) in water. Compared with F127@BDBF NPs, BDBF NRs exhibited stronger orange fluorescence with a higher FQY of 23.3% and similar singlet oxygen(1O2) generation capability. BDBF NRs were further modified with F127 to form BDBF@F127 NRs with the same 1O2 generation ability as BDBF NRs. The three nanostructures exhibited a higher 1O2 production capacity than BDBF molecule in dissolved state and favorable stability in an aqueous solution as well as under physiological condition. In vitro photocytotoxicity experiments indicated that the three nanostructures inhibited tumor cell proliferation effectively.Therefore, to construct eligible nanostructures with a high FQY and 1O2 generation ability, simple self-assembly can serve as a valuable method to prepare photosensitizers with enhanced PDT.

Optimization design of optical waveguide in mach-zehnder electro-optical polymer modulator

In order to reduce transmission loss of the optical waveguide in Mach-Zehnder (M-Z) electro-optical (EO) polymer modulator,the basic iterative formula of semi-vector finite-difference beam propagation method (FD-BPM) is obtained from the scalar wave equation. The transition waveguide is combined with S-type bend branch waveguide for the M-Z EO modulator in the branch waveguide. The effects of structure parameters such as ridge width,length of the branch waveguide and interferometer spacing on the transmission loss are systematically studied by using the semi-vector FD-BPM method. The structure is optimized as an S-sine bend branch waveguide,with rib width w=7μm,length of branch waveguide L=1200μm and interferometer spacing G=22 μm. The results show that the optimized structure can reduce transmission loss to 0.083 dB,which have a certain reference value to the design of optical waveguide in M-Z polymer modulator.

Biocompatible organic dots with aggregation-induced emission for in vitro and in vivo fluorescence imaging

Fluorescent probes play a key role in modern biomedical research. As compared to inorganic quantum dots (QDs) composed with heavy metal elements, organic dye-based fluorescent nanoparticles have higher biocompatibility and are richer in variety. However, traditional organic fluorophores tend to quench fluorescence upon aggregation, which is known as aggregation-caused quenching (ACQ) effect that hinders the fabrication of highly emissive fluorescent nanoparticles. In this work, we demonstrate the synthesis of organic fluorescent dots with aggregation-induced emission (AIE) in far-red/near-infrared (FA/NIR) region. A conventional ACQ-characteristic fluorescent dye, 3,4:9,10-tetracarboxylic perylene bisimide (PBI), is converted into an AIE fluorogen through attaching two tetraphenylethylene (TPE) moieties. The fluorescent dots with surface folic acid groups are fabricated from PBI derivative (DTPEPBI), showing specific targeting effect to folate receptor-overexpressed cancer cells. In vivo studies also suggest that the folic acid-functionalized AIE dots preferentially accumulate in the tumor site through enhanced permeability and retention (EPR) effect and folate receptor-mediated active targeting effect. The low cyto-toxicity, good FR/NIR contrast and excellent targeting ability in in vitro/in vivo imaging indicate that the AIE dots have great potentials in advanced bioimaging applications.