109 results match your criteria: "Shenzhen University Shenzhen 518060 China.[Affiliation]"

Ag(i) emitters with ultrafast spin-flip dynamics for high-efficiency electroluminescence.

Chem Sci

November 2024

College of Chemistry and Molecular Sciences, Hubei Key Laboratory on Organic and Polymeric Optoelectronic Materials, Wuhan University Wuhan 430072 China

Carbene-metal-amide (CMA) complexes are appealing emitters for organic light-emitting diodes (OLEDs). However, little is known about silver(i)-CMA complexes, particularly electroluminescent ones. Here we report a series of Ag(i)-CMA complexes prepared using benzothiophene-fused carbazole derivatives as amide ligands.

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Dual back interface engineering optimized charge carrier dynamics in Sb(S,Se) photocathodes for efficient solar hydrogen production.

Chem Sci

December 2024

Shenzhen Key Laboratory of Advanced Thin Films and Applications, Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, State Key Laboratory of Radio Frequency Heterogeneous Integration, College of Physics and Optoelectronic Engineering, Shenzhen University Shenzhen 518060 China

Antimony sulfoselenide (Sb(S,Se)) is a promising sunlight absorber material for solar energy conversion in photovoltaic (PV) cells and photoelectrochemical (PEC) photoelectrodes due to its excellent photoelectric properties. However, the obtained thin-film and back contact properties significantly influence the PEC performance of photocathodes, causing severe bulk recombination, carrier transport loss, and deteriorating half-cell solar-to-hydrogen (HC-STH) efficiency. This study introduces an intriguing dual back interface engineering strategy for Sb(S,Se) photocathodes by incorporating an intermediate MoO layer and a secondary carrier transport channel of Au to strengthen charge carrier dynamics.

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A switchable magnetic resonance imaging nanoplatform for microRNA imaging.

Chem Sci

December 2024

Marshall Laboratory of Biomedical Engineering, Precision Medicine and Health Research Institute, Research Center for Biosensor and Nanotheranostic, Guangdong Key Laboratory of Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering, Shenzhen University Medical School, Shenzhen University Shenzhen 518060 China

Aberrant microRNA (miRNA) expression is associated with various types of carcinogenesis, making miRNA a promising candidate for diagnostic and therapeutic biomarkers. However, miRNA diagnostics remains a significant challenge owing to the various biological barriers. Herein, we report a novel miRNA imaging probe consisting of PEG-polylysine-PNIPAM polymer matrix-modified small FeO (PAA-FeO-DNA@PPP) nanoparticles with an improved circulatory half-life, efficient tissue permeability, and enhanced tumor accumulation, for miRNA magnetic resonance imaging (MRI).

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The development of flexible, cost-effective, highly efficient, and reliable humidity monitoring sensors is in high demand owing to their wide-range of applications in industrial domains. In this study, a humidity sensor was fabricated based on graphite/zinc oxide nanoparticle (G/ZnO-NP)-coated cellulose paper. A bar device was designed using computer software, and its sketch was printed on cellulose paper, with graphite bars then added using the pencil-drawing method, and then ZnO-NP paste was coated on the graphite patterns.

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Correction: Second-shell modulation on porphyrin-like Pt single atom catalysts for boosting oxygen reduction reaction.

Chem Sci

November 2024

Shenzhen Key Laboratory of Micro/Nano-Porous Functional Materials (SKLPM), SUSTech-Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM-JIL), Department of Chemistry and Department of Materials Science and Engineering, Southern University of Science and Technology (SUSTech) Shenzhen 518055 China

Article Synopsis
  • This text is a correction to a previously published article identified by the DOI: 10.1039/D4SC03369H.
  • The correction likely addresses errors or inaccuracies found in the original article.
  • The purpose is to ensure that the scientific record is accurate and reflects the correct information. *
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Second-shell modulation on porphyrin-like Pt single atom catalysts for boosting oxygen reduction reaction.

Chem Sci

October 2024

Shenzhen Key Laboratory of Micro/Nano-Porous Functional Materials (SKLPM), SUSTech-Kyoto University Advanced Energy Materials Joint Innovation Laboratory (SKAEM-JIL), Department of Chemistry and Department of Materials Science and Engineering, Southern University of Science and Technology (SUSTech) Shenzhen 518055 China

The first coordination shell is considered crucial in determining the performance of single atom catalysts (SACs), but the significance of the second coordination shell has been overlooked. In this study, we developed a post-doping strategy to realize predictable and controlled modulation on the second coordination shell. By incorporating a P atom into the second coordination shell of a porphyrin-like Pt SAC, the charge density at the Fermi level of Pt single atom increases, enhancing its intrinsic activity.

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High-performance deep-blue electroluminescence from multi-resonance TADF emitters with a spirofluorene-fused double boron framework.

Chem Sci

October 2024

Shenzhen Key Laboratory of New Information Display and Storage Materials, College of Materials Science and Engineering, Shenzhen University Shenzhen 518060 China

Article Synopsis
  • The study focuses on creating new multi-resonance thermally activated delayed fluorescence (MR-TADF) materials for deep-blue light emission to enhance device efficiency in OLED technology.
  • Researchers combine MR-TADF frameworks with 9,9'-spirobifluorene units to improve structural stability and avoid quenching issues that often reduce performance.
  • The resulting emitters demonstrate superior properties, including narrowband deep-blue emission, high photoluminescence quantum yield, and a maximum external quantum efficiency (EQE) of 39.0%, leading to improved performance in OLED applications.
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Biomimetic engineering of a neuroinflammation-targeted MOF nanozyme scaffolded with photo-trigger released CO for the treatment of Alzheimer's disease.

Chem Sci

August 2024

Laboratory of Chemical Biology and State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences Changchun Jilin 130022 P. R. China

Alzheimer's disease (AD) is one of the most fatal and irreversible neurodegenerative diseases, which causes a huge emotional and financial burden on families and society. Despite the progress made with recent clinical use of inhibitors of acetylcholinesterase and amyloid-β (Aβ) antibodies, the curative effects of AD treatment remain unsatisfactory, which is probably due to the complexity of pathogenesis and the multiplicity of therapeutic targets. Thus, modulating complex pathological networks could be an alternative approach to treat AD.

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Concurrent near-infrared-II (NIR-II) fluorescence imaging (FLI) and photoacoustic imaging (PAI) holds tremendous potential for effective disease diagnosis owing to their combined benefits and complementary features, in particular on the basis of a single molecule. However, the simultaneous guarantee of high-quality NIR-II FLI and PAI is recognized to be challenging impeded by the competitive photophysical processes at the molecular level. Herein, a simple organic fluorophore, namely T-NSD, is finely engineered with facile synthetic procedures through delicately modulating the rigidity and electron-withdrawing ability of the molecular acceptor.

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Sonodynamic therapy (SDT), as a novel non-invasive cancer treatment modality derived from photodynamic therapy (PDT), has drawn much attention due to its unique advantages for the treatment of deep tumors. Zinc-based complexes have shown great clinical prospect in PDT due to their excellent photodynamic activity and biosafety. However, their application in SDT has lagged seriously behind.

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A planar electronic acceptor motif contributing to NIR-II AIEgen with combined imaging and therapeutic applications.

Chem Sci

May 2024

Department of Chemistry, Hong Kong Branch of Chinese National Engineering Research Center for Tissue Restoration and Reconstruction, Guangdong-Hong Kong-Macau Joint Laboratory of Optoelectronic and Magnetic Materials, The Hong Kong University of Science and Technology Clear Water Bay, Kowloon Hong Kong 999077 China.

Designing molecules with donor-acceptor-donor (D-A-D) architecture plays an important role in obtaining second near-infrared region (NIR-II, 1000-1700 nm) fluorescent dyes for biomedical applications; however, this always comes with a challenge due to very limited electronic acceptors. On the other hand, to endow NIR-II fluorescent dyes with combined therapeutic applications, trivial molecular design is indispensable. Herein, we propose a pyrazine-based planar electronic acceptor with a strong electron affinity, which can be used to develop NIR-II fluorescent dyes.

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Two-dimensional radial-π-stacks in solution.

Chem Sci

April 2024

Department of Chemistry, College of Chemistry and Chemical Engineering, MOE Key Laboratory of Spectrochemical Analysis and Instrumentation, Xiamen University Xiamen 361005 P. R. China.

Highly organized π-aggregate architectures can strongly affect electronic couplings, leading to important photophysical behaviors. With the escalating interest in two-dimensional (2D) materials attributed to their exceptional electronic and optical characteristics, there is growing anticipation that 2D radial-π-stacks built upon radial π-conjugation nanorings, incorporating intra- and inter-ring electronic couplings within the confines of a 2D plane, will exhibit superior topological attributes and distinct properties. Despite their immense potential, the design and synthesis of 2D π-stacks have proven to be a formidable challenge due to the insufficient π-π interactions necessary for stable stacking.

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Facile fabrication of a graphene-based chemical sensor with ultrasensitivity for nitrobenzene.

RSC Adv

March 2024

State Key Laboratory of Radio Frequency Heterogeneous Integration, College of Electronics and Information Engineering, Shenzhen University Shenzhen 518060 China.

Chemical sensors have a wide range of applications in a variety of industries, particularly for sensing volatile organic compounds. This work demonstrates the fabrication of a chemical sensor based on graphene deposited on Cu foils using low-pressure chemical vapor deposition, following its transfer on oxidized silicon through a wet etching method. Scanning electron microscopy, Raman spectroscopy and UV-vis spectroscopy of the transferred graphene were performed.

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Comparison of the penetration depth in mouse brain through 3PF imaging using AIE nanoparticle labeling and THG imaging within the 1700 nm window.

Nanoscale Adv

January 2024

Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Physics and Optoelectronic Engineering, Shenzhen University Shenzhen 518060 China

Article Synopsis
  • 3-Photon microscopy (3PM) at 1700 nm offers greater brain imaging depth due to reduced tissue attenuation compared to other wavelengths.
  • Previous studies have investigated penetration depth at various exciting wavelengths, but comparisons within the 1700 nm range were lacking due to limited laser sources and fluorescent label characterization.
  • The research demonstrates that 3PM at 1700 nm provides superior imaging depth in mouse brains, confirming it as the optimal wavelength for deep tissue visualization.
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The utilization of microfluidic technology for miniaturized and efficient particle sorting holds significant importance in fields such as biology, chemistry, and healthcare. Passive separation methods, achieved by modifying the geometric shapes of microchannels, enable gentle and straightforward enrichment and separation of particles. Building upon previous discussions regarding the effects of column arrays on fluid flow and particle separation within microchips, we introduced a column array structure into an H-shaped microfluidic chip.

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Through-space charge transfer (TSCT) has been proven effective for designing thermally activated delayed fluorescence (TADF) emitters due to the separation of the frontier molecular orbitals. Although tuning of the interaction between the donor and acceptor by controlling the conformation is known to be crucial for the photophysical properties of TSCT excited states, it remains a challenge to realize efficient red and deep-red emissions. Herein, we designed two TSCT molecules, namely TPXZ-QX and TPXZ-2QX, by using oxygen-bridged triphenylamine (TPXZ) as the electron donor with enhanced planarity and electron-donating capability.

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A CuCl/(,)-Ph-BPE-catalyzed enantioselective hydroallylation of 2-chromenes and 2-thiochromenes with allylic phosphate electrophiles is developed, which enables highly efficient and atom-economical asymmetric access to a series of 4-allyl chromanes and thiochromanes in high yields (up to 91%) with excellent enantioselectivities (up to 99% ee). These valuable chiral chromane and thiochromane products can serve as crucial intermediates for accessing bioactive compounds containing oxygen and sulfur atoms. In addition, the antioxidant and anti-inflammatory effects of various chromanes and thiochromanes were investigated in RAW 264.

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Electrodes that offer quick ion transport, a large surface area, and excellent electrical conductivity support high performance aqueous rechargeable lithium batteries. LiFePO (LFP) nanoparticles have been successfully coated with carbon by a chemical sol-gel route, and assembled on graphite by an ultrasonication method to acquire LFP/C/graphite. This LFP/C/graphite composite exhibits exceptional electrochemical performance at various current densities (1C to 20C).

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Azonaphthalenes have been verified as a class of effective arylation reagents in a variety of asymmetric transformations. Here a highly efficient approach to construct triaryl-substituted all-carbon quaternary stereocenters through chiral phosphoric acid-catalyzed enantioselective arylation of 3-aryl-2-oxindoles with azonaphthalenes is disclosed. This chemistry is scalable and displays excellent functional group tolerance, furnishing a series of 3,3-disubstituted 2-oxindole derivatives in good yields with excellent enantiocontrol.

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Development of room-temperature sodium-sulfur batteries is significantly hampered by the shuttle effect of soluble intermediates and intrinsically sluggish conversion kinetics. In this work, a double design host and guest strategy (, implantation of a polar VO adsorbent into a carbon substrate and selenium doping of a sulfur guest) is proposed to synergistically reinforce the electrochemical properties of sulfur electrodes in sodium ion storage. The VO adsorbent efficiently immobilizes sulfur species strong polar-polar interactions, while the selenium dopant improves the electronic conductivity of sulfur cathodes and accelerates the redox conversion of sulfur cathodes.

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The development of facile polymerizations toward functional heterocyclic polymers is of great significance for chemistry and materials science. As an important class of heterocyclic polymers, polyoxadiazoles (PODs) have found applications in various fields. However, the synthetic difficulties of PODs greatly restrict their structural diversity and property investigation.

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Highly biocompatible chlorin e6-poly(dopamine) core-shell nanoparticles for enhanced cancer phototherapy.

Nanoscale Adv

October 2022

Guangdong Key Laboratory for Biomedical Measurements and Ultrasound Imaging, School of Biomedical Engineering, Health Science Center, Shenzhen University Shenzhen 518060 China

Cancer is a life-threatening disease worldwide. Although several approaches, such as surgery, chemotherapy, and radiotherapy, have been proven effective for many patients in clinics, they usually suffer from drug resistance, severe toxic-side effects, patient discomfort, and sometimes, unsatisfactory efficacies. In recent years, phototherapy, as a less invasive but effective therapeutic method, has brought hope for cancer treatment.

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Technical bottlenecks of polyselenide shuttling and material volume variation significantly hamper the development of emerging sodium-selenium (Na-Se) batteries. The nanopore structure of substrate materials is demonstrated to play a vital role in stabilizing Se cathodes and approaching superior Na-ion storage properties. Herein, an ideal nanorod-like trimodal hierarchical porous carbon (THPC) host is fabricated through a facile one-step carbonization method for advanced Na-Se batteries.

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