Publications by authors named "Yingquan Zou"

The primary focus of photopolymerization research is to advance highly efficient visible photoinitiating systems (PISs) as alternatives to conventional ultraviolet (UV) photoinitiators. We developed four multiresonance emitters (BIC-pCz, BNO1, BO-DICz, and TPABO-DICz) to sensitize iodonium salt (Iod) and initiate free-radical and cationic photopolymerization under visible light for the first time. The TPABO-DICz/Iod system achieved a double-bond conversion of over 70% within just 4 s of exposure to green light (520 nm), while the BNO1/Iod system achieved a double-bond conversion exceeding 50% with 10 s of exposure to red light (630 nm).

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High-performance photoinitiators (PIs) are essential for ultraviolet-visible (UV-Vis) light emitting diode (LED) photopolymerization. In this study, a series of coumarin ketoxime esters (COXEs) with electron-donating substituents (-butyl, methoxy, dimethylamino and methylthio) were synthesized to study the structure/reactivity/efficiency relationships for substituents for the photoinitiation performance of PIs. The introduction of heteroatom electron-donating substituents leads to a redshift in the COXE absorption of more than 60 nm, which matches the UV-Vis LED emission spectra.

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Graphene quantum dots usually suffer from serious fluorescence quenching in aggregates and the solid state due to easy agglomeration and aggregation-induced quenching, which seriously restrict their practical applications. An ingenious strategy to kill three birds with one stone, the ultraviolet (UV) photolithography technique, was studied, and blue-emitting reduced graphene oxide quantum dot (rGOQD)-based light emitting diodes (LEDs) with efficient solid state emission were first fabricated using UV photolithography. First, rGOQDs were prepared by the in situ photoreduction of GOQDs by using the photoinitiator phenyl bis(2,4,6-trimethylbenzoyl)phosphine oxide with 395 nm UV LED exposure.

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NIR-sensitized cationic polymerization proceeded with good efficiency, as was demonstrated with epoxides, vinyl ether, and oxetane. A heptacyanine functioned as sensitizer while iodonium salt served as coinitiator. The anion adopts a special function in a series selected from fluorinated phosphates (a: [PF ] , b: [PF (C F ) ] , c: [PF (n-C F ) ] ), aluminates (d: [Al(O-t-C F ) ] , e: [Al(O(C F )CH ) ] ), and methide [C(O-SO CF ) ] (f).

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Cyanines comprising either a benzo[e]- or benzo[c,d]indolium core facilitate initiation of radical photopolymerization combined with high power NIR-LED prototypes emitting at 805 nm, 860 nm, or 870 nm, while different oxime esters function as radical coinitiators. Radical photopolymerization followed an initiation mechanism based on the participation of excited states, requiring additional thermal energy to overcome an existing intrinsic activation barrier. Heat released by nonradiative deactivation of the sensitizer favored the system, even under conditions where a thermally activated photoinduced electron transfer controls the reaction protocol.

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Considering the lack of precision in transforming measured micro-electro-mechanical system (MEMS) accelerometer output signals into elevation signals, this paper proposes a bridge dynamic displacement reconstruction method based on the combination of ensemble empirical mode decomposition (EEMD) and time domain integration, according to the vibration signal traits of a bridge. Through simulating bridge analog signals and verifying a vibration test bench, four bridge dynamic displacement monitoring methods were analyzed and compared. The proposed method can effectively eliminate the influence of low-frequency integral drift and high-frequency ambient noise on the integration process.

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In this work, ZnO nanoparticles-reduced graphene oxide (rGO) composites were fabricated via a novel one-step photochemical method. The developed nanocomposite offered high photodegradation efficiency of methylene blue (MB) under UV and visible light. In the proposed route, the reduction of graphene oxide (GO) and formation of ZnO nanoparticles occurred simultaneously, which results in high synthesis efficiency of ZnO/rGO nanocomposites.

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The title compound, [Eu(C(9)H(9)O(4))(3)](n) or [Eu(2,3-DMOBA)(3)](n), where 2,3-DMOBA is 2,3-dimethoxybenzoate, is an infinite one-dimensional non-centrosymmetric coordination polymer. The unique Eu(III) atom is bridged by six carboxylate ligands; it is ennea-coordinated and has a distorted tricapped trigonal prism geometry. The Eu-O distances are in the range 2.

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