Qiang Zhang

ORCID: 0000-0002-0186-827X
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Conducting polymers and applications
  • Luminescence and Fluorescent Materials
  • Organic Light-Emitting Diodes Research
  • Perovskite Materials and Applications
  • Nanoplatforms for cancer theranostics
  • Molecular Sensors and Ion Detection
  • Analytical Chemistry and Sensors
  • Synthesis and properties of polymers
  • Metal-Organic Frameworks: Synthesis and Applications
  • Advanced Photocatalysis Techniques
  • Thin-Film Transistor Technologies
  • Nanowire Synthesis and Applications
  • Covalent Organic Framework Applications
  • Photoacoustic and Ultrasonic Imaging
  • Advanced biosensing and bioanalysis techniques
  • Photodynamic Therapy Research Studies
  • Advanced Polymer Synthesis and Characterization
  • Asymmetric Synthesis and Catalysis
  • Sulfur-Based Synthesis Techniques
  • Synthesis and Characterization of Heterocyclic Compounds
  • biodegradable polymer synthesis and properties
  • Membrane Separation and Gas Transport
  • Synthesis and pharmacology of benzodiazepine derivatives
  • Biochemical Acid Research Studies

Nankai University
2015-2024

State Key Laboratory of Luminescent Materials and Devices
2024

Tianjin University of Technology
2015-2024

South China University of Technology
2021-2024

Heilongjiang University
2024

State Key Laboratory of Polymer Physics and Chemistry
2024

Chinese Academy of Sciences
2024

Changchun Institute of Applied Chemistry
2024

Minzu University of China
2022

Changzhou University
2020-2022

Nonfullerene acceptor FDICTF (2,9-bis(2methylene-(3-(1,1-dicyanomethylene)indanone))-7,​12-​dihydro-​4,​4,​7,​7,​12,​12-​hexaoctyl-​4H-​cyclopenta[2″,​1″:5,​6;3″,​4″:5',​6']​diindeno[1,​2-​b:1',​2'-​b']dithiophene) modified by fusing the fluorene core in a precursor, yields 10.06% high power conversion efficiency, and demonstrates that ladder fused backbone A-D-A structure molecules is an effective design strategy for high-performance nonfullerene acceptors.

10.1002/adma.201604964 article EN Advanced Materials 2016-11-28

Abstract Dual phototherapy, including photodynamic therapy (PDT) and photothermal (PTT), is regarded as a more effective method for cancer treatment than single PDT or PTT. However, development of component near‐infrared (NIR) triggered agents efficient dual phototherapy remains challenge. Herein, simple strategy to develop dual‐functional small‐molecules‐based photosensitizers combined PTT proposed through: 1) finely modulating HOMO–LUMO energy levels regulate the intersystem crossing (ISC)...

10.1002/adfm.201910301 article EN Advanced Functional Materials 2020-02-24

Highly regioregular conducting polymers such as poly(3-substituted thiophene)s (rrP3STs) are an important class of π-conjugated that can be used in plastic electronic devices solar cells and field-effect transistors. But the current state art syntheses rrP3STs all involve transition-metal-catalyzed cross-coupling a heteroaryl halide or pseudohalide with organometallic reagent. In this work, efficient mild method was developed using direct sp2 C–H bonds. More importantly, not only gave...

10.1021/acs.macromol.7b02390 article EN Macromolecules 2018-01-02

Forming high-performance IDTBT film with large aggregations tight π–π stacking via fast aggregation between backbones during formation by adjusting the solubility difference R a (b–s) of backbone and side chain in solvent.

10.1039/d4tc00148f article EN Journal of Materials Chemistry C 2024-01-01

A simple, mild, atom economical homopolymerization method through Pd-catalyzed oxidative C–H/C–H coupling was developed for the preparation of a series 5-alkyl[3,4-<italic>c</italic>]thienopyrrole-4,6-dione-based conjugated polymers.

10.1039/c4cc06284a article EN Chemical Communications 2014-01-01

A new ratiometric probe for ATP was designed based on the binding-induced modulation of FRET coupled with ACQ sensing mechanism.

10.1039/c6py02001a article EN Polymer Chemistry 2017-01-01

A water-soluble PDIs-based polymeric chemosensor L displays a turn-on response selective to Fe<sup>3+</sup>, which allows facile monitoring of the Fe<sup>3+</sup>/Fe<sup>2+</sup>transition and intracellular Fe<sup>3+</sup>imaging.

10.1039/c6ra08267j article EN RSC Advances 2016-01-01

Polyamide plays a pivotal role in engineering thermoplastics. Constrained by the harsh conditions and arduous procedures for its industrial synthesis, developing facile synthesis of polyamides is still challengeable holds profound significance. Herein, we successfully utilized water as one monomers to synthesize functional under ambient conditions. A powerful multicomponent polymerization water, isocyanides, chlorooximes was established phosphate-buffered saline. Soluble thermally stable...

10.1002/anie.202410846 article EN Angewandte Chemie International Edition 2024-08-06

PDTON, exhibiting either hole transporting or reducing electrode WF, can be utilized as a ‘universal’ buffer layer material.

10.1039/c7ee03275g article EN Energy & Environmental Science 2018-01-01

Photothermal therapy (PTT) has received constant attention as an efficient cancer method due to locally selective treatment, which is not affected by the tumor microenvironment. In this study, a novel 880 nm near-infrared (NIR) laser-triggered photothermal agent (PTA), 3TT-IC-4Cl, was used for PTT of in deep tissue. Folic acid (FA) conjugated amphiphilic block copolymer (folic acid-polyethylene glycol-poly (β-benzyl-L-aspartate)10, FA-PEG-PBLA10) employed encapsulate 3TT-IC-4Cl...

10.3390/nano11030773 article EN cc-by Nanomaterials 2021-03-18

Single organic small molecule-based nanoparticles (CNPs) with strong responses within the NIR-II (1000-1350 nm) bio-window were prepared, and successfully applied as a highly efficient photothermal antibacterial agent for first time. CNPs exhibit an outstanding bacteria inhibition efficiency of almost 100% against Staphylococcus aureus (S. aureus) high conversion (PTCE) circa 49% under laser irradiation (1064 8 min.

10.1039/d2cc00863g article EN Chemical Communications 2022-01-01

The PTB7-Th/PC<sub>71</sub>BM-based PSCs exhibit a significantly improved PCE of 8.33% and device stability for the halogen-free solid ROPD additive.

10.1039/d0tc04096g article EN Journal of Materials Chemistry C 2020-01-01

Diseases caused by antibiotic-resistant pathogenic bacteria are seriously threatening human health. Therefore, the development of new antimicrobial materials and treatment strategies is urgently needed. Herein, we designed synthesized a donor–acceptor (D-A) structured conjugated polymer Poly(TP-T), which functionalized with positively charged side chain for selective contact bacterial cells through electrostatic interaction rapid efficient near-infrared light-activated photothermal therapy....

10.1021/acsapm.3c03143 article EN ACS Applied Polymer Materials 2024-02-26

The separation of acetylene from carbon dioxide is challenging due to their almost identical molecular sizes and volatilities. Metal-organic frameworks (MOFs) in general are strong candidates for the gas mixtures owing presence functional pore surfaces that can selectively capture specific target molecules. Herein, we report a stable easily synthesized bismuth-based MOF, Bi-BTC, which achieve dioxide. We performed detailed analysis sorption properties Bi-MOF. Bi-BTC shows good adsorption capacities C

10.1039/d4dt00246f article EN Dalton Transactions 2024-01-01

We are developing both copolymers with quinoxaline (Qx) as acceptor units by fine tuning the side chains halogen atom chlorine (Cl) and flexible alkyl engineering for efficient non-fullerene polymer solar cells.

10.1039/d0qm00826e article EN Materials Chemistry Frontiers 2020-12-10

Four D-π-A conjugated polymers, namely P1–P4, which contain benzotriazole building blocks in their backbone as acceptor, are synthesized via palladium-catalyzed direct C-H cross-coupling polycondensation of 5,6-difluorobenzotriazole with different thiophene derivatives, including 3-octylthiophene, 2,2’-bithiophene, thieno[3,4-b][1,4]dioxine, and 4,4-dioctyl-4H-silolo-[3,2-b:4,5-b’]dithiophene donor units, respectively. Taking the polymer P1 an example, chemical structure is demonstrated by...

10.3390/polym13020254 article EN Polymers 2021-01-14
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