Li Chen

ORCID: 0009-0007-3208-5220
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Conducting polymers and applications
  • Perovskite Materials and Applications
  • Organic Light-Emitting Diodes Research
  • Liquid Crystal Research Advancements
  • High voltage insulation and dielectric phenomena
  • Advanced Measurement and Detection Methods
  • Thin-Film Transistor Technologies
  • Nanomaterials for catalytic reactions
  • Heat Transfer and Boiling Studies
  • Advanced Memory and Neural Computing
  • Occupational and environmental lung diseases
  • CO2 Reduction Techniques and Catalysts
  • Catalysis for Biomass Conversion
  • Fluid Dynamics and Thin Films
  • Drilling and Well Engineering
  • Luminescence and Fluorescent Materials
  • Supramolecular Chemistry and Complexes
  • Carbon dioxide utilization in catalysis
  • Rock Mechanics and Modeling
  • Catalytic Processes in Materials Science
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Molecular Junctions and Nanostructures
  • Electrostatic Discharge in Electronics
  • Advanced Polymer Synthesis and Characterization

Hong Kong University of Science and Technology
2022-2025

Wuhan University of Technology
2018-2024

University of Hong Kong
2022-2024

State Key Laboratory of Medicinal Chemical Biology
2024

Nankai University
2024

Xiangtan University
2010-2022

Xi'an Technological University
2019

Hebei University of Technology
2018

Nanjing University of Information Science and Technology
2018

Abstract Cyanation is a common chemical modification strategy to fine‐tune the energy levels and molecular packing of organic semiconductors, especially materials used in solar cells (OSCs). Generally, cyanation modify end groups high‐performance small‐molecule acceptors (SMAs). However, has not been investigated on central backbone SMAs, which could introduce stronger intermolecular interaction enhance π–π stacking for rapid charge transport. This paper, first time, reports new...

10.1002/aenm.202400285 article EN Advanced Energy Materials 2024-05-11

Two star-shaped helical perylene diimide (PDI) electron acceptors TPDI2 and FTPDI2 were designed synthesized for nonfullerene organic solar cells (OSCs). The integration of PDIs into a three-dimensional structure provides new strategy to tune the intermolecular interactions, as-cast blend films with PTB7-Th show favorable morphology as well efficient charge transfer separation, evidenced by femtosecond transient absorption (fs-TA) spectroscopy studies. A trade-off between suppressing...

10.1021/acsami.8b06126 article EN ACS Applied Materials & Interfaces 2018-07-27

We developed a novel Y-series small molecule acceptor by adopting benzoselenadiazole central core and alkoxy side chains on the β-position of thiophene moieties, inducing boost in performance due to upshifted energy levels optimized morphology.

10.1039/d3ta04364a article EN Journal of Materials Chemistry A 2023-01-01

A small-molecule/fullerene acceptor alloy improved the PCE and stability of PBDB-T/PC<sub>71</sub>BM/IDT-OT ternary PSCs.

10.1039/d0tc00329h article EN Journal of Materials Chemistry C 2020-01-01

The ionic wind has good application prospects in the fields of air flow control and heat transfer enhancement. key for successful applications is how to improve velocity increase active area wind. This paper designed a needle array-mesh type electrohydrodynamic (EHD) gas pump. use array electrode where corona discharge started simultaneously could enlarge area. by placing several single-stage generators series appropriately, called as serial staged generator. maximum average 16.1 m/s...

10.1088/1009-0630/13/6/11 article EN Plasma Science and Technology 2011-12-01

Abstract A well‐defined structure liquid crystal heptakis [6‐deoxy‐6‐(1‐H‐1,2,3‐triazol‐4‐yl)(methyl)6‐(4‐methoxybiphenyl‐4′‐yloxy) hexanoyl]‐β‐cyclodextrin (H6B‐β‐CD) was synthesized from propargyl 6‐(4‐methoxybiphenyl‐4′‐yloxy) hexanoate (P6B) and (6‐deoxy‐6‐azido)‐β‐cyclodextrin ((N 3 ) 7 ‐β‐CD) by click reaction. The chemical of H6B‐β‐CD confirmed 1 H NMR, FTIR, MALDI‐TOF MS. thermal stability the compound investigated thermogravimetric analysis (TGA). crystalline behavior studied...

10.1002/pola.24060 article EN Journal of Polymer Science Part A Polymer Chemistry 2010-05-24

Adding a small‐molecule donor (SMD) to state‐of‐the‐art nonfullerene organic solar cells (OSCs) is demonstrated as useful strategy construct ternary cells, SMDs typically have high crystallinity and can tune charge transport properties of OSCs. However, the absorption most overlaps with typical polymers (e.g., PM6), which against general guidelines adopting materials complementary in Herein, state‐of‐art (BTR‐Cl) by linking beta position outer thiophene alpha inner unit intentionally...

10.1002/solr.202200386 article EN Solar RRL 2022-06-21

Abstract Covalent functionalization of multi‐walled carbon nanotubes (MWNTs) with side‐chain azobenzene liquid crystalline poly{6‐[4‐(4‐methoxyphenylazo)phenoxy]hexyl methacrylate} (PMMAZO) was successfully achieved via atom transfer radical polymerization. The resultant samples were characterized using Fourier transform infrared spectroscopy, thermogravimetric analysis and transmission electron microscopy. results differential scanning calorimetry polarized optical microscopy show that the...

10.1002/pi.2917 article EN Polymer International 2010-09-13

Combining the halogenation on A group of dithienocyclopentafluorene-based A–D–A acceptors and variation paired polymer donor is an effective strategy to enhance device efficiency by balancing photovoltaic parameters.

10.1039/d0tc05178k article EN Journal of Materials Chemistry C 2021-01-01

In this contribution, a series of A-π-D-π-A small molecules (SMs), IPY-T-IC, IPY-T-ICCl, and IPY-T-ICF, containing the central donor unit (D) 6,12-dihydro-diindolo[1,2-b:10,20-e]pyrazine (IPY), π-conjugated bridge thiophene, end-accepting group (A) 3-(dic yanomethylidene)indol-1-one, 5,6-dichloro-3-(dicyanomethylidene)indol-1-one, or 5,6-difluoro-3-(dicyanomethylene)indol-1-one, were developed, characterized, employed as acceptor materials for polymer solar cells (PSCs). Influences different...

10.1021/acsami.9b17185 article EN ACS Applied Materials & Interfaces 2019-12-11

Development of high-performance small-molecular acceptors (SMAs) and an eco-friendly simple device fabrication procedure is very crucial for scalable production polymer solar cells (PSCs) in the future. Here, we designed synthesized two new nonacyclic SMAs (IPYT-IC IPYT-ICF) featuring A–DA′D–A-type molecular configuration, which electron-deficient 6,12-dihydro-diindolo[1,2-b:10,20-e]pyrazine (IPY) moiety was used as additional acceptor unit (A′) fused with electron-rich...

10.1021/acs.jpcc.0c07557 article EN The Journal of Physical Chemistry C 2020-09-18

N-type benzimidazole and difluorobenzimidazole fused perylene diimide dimer semiconductors were synthesized a remarkable electronic mobility of 0.13 cm 2 V −1 s was obtained for FMBI-PDI2-based organic field-effect transistor (OFET).

10.1039/d2tc05095a article EN Journal of Materials Chemistry C 2023-01-01

Materials Synthesis and Processing Polycyclic aromatic hydrocarbon (PAH) diimides are indispensable candidates for n-type organic semiconductors in optoelectronic devices. Developing new PAH diimide building blocks of remarkable significance material diversity further advance semiconductors. In this contribution, 4,5,8,9-picene (PiDI) was designed synthesized. Controllable stepwise bromination PiDI were accomplished to afford 13-monobromo-, 13,14-dibromo-, 2,13,14-tribromo-...

10.1002/chem.202300480 article EN Chemistry - A European Journal 2023-03-02

Helical perylene diimide-based (hPDI) acceptors have been established as one of the most promising candidates for non-fullerene organic solar cells (OSCs). In this work, we report a novel hPDI-based molecule, hPDI 2 -CN , an electron acceptor OSCs. Combining with low-bandgap polymeric donor (PTB7-Th), blending film morphology exhibited high sensitivity to various treatments (such thermal annealing and addition solvent additives), evidenced by atomic force microscope studies. The power...

10.1098/rsos.172041 article EN cc-by Royal Society Open Science 2018-05-01

Cu/Co3O4-ZrO2 catalyst was synthesized by a simple co-precipitation method, and its self-oxidation behavior after reduction reduced the particle size of Co3O4. demonstrated high performance during dehydrogenation diethanolamine, reaching 96% yield iminodiacetic in 30 min. The characterized XRD, XPS, TEM, SEM, H2-TPR. results showed that strong Cu-oxide interactions, co-catalysis biactive components, higher number oxygen vacancies were responsible for enhanced catalytic activity...

10.1016/j.catcom.2020.106043 article EN cc-by-nc-nd Catalysis Communications 2020-05-11

Subtle modification of the electron-withdrawing end group (A) small-molecule acceptors (SMAs) plays an important role in regulating structure, optoelectronic properties, and device performance. To obtain SMAs for nonhalogenated solvent-processing devices, we develop two A–D–A (IT-ClBr IT-FBr) based on indacenodithieno[3,2-b]thiophene (D) by employing hybrid dihalogenated 1,1-dicyanomethylene-3-indanone (IC-ClBr IC-FBr) as A groups. The effects groups solubility, photoelectrochemical...

10.1021/acsaem.2c01249 article EN ACS Applied Energy Materials 2022-06-23

We perform density functional theory calculations to investigate the polaron pair (charge transfer state) photo-generation in donor-acceptor oligomer methyl-capped (4,7-benzo[2,1,3]thiadiazole-2,6-(4,4-bis(2-ethylhexyl)-4H-cyclopenta[1,2-b;3,4-b′]dithiophene-4, 7-benzo[2,1,3]thiadiazole) (CPDTBT). Results show that effective of charge state can happen CPDTBT dimer when group 4,7-benzo[2,1,3]thiadiazole (BT) one monomer deviates against conjugated plane (onset torsion angle is about 20°). The...

10.1063/1674-0068/31/cjcp1707151 article EN Chinese Journal of Chemical Physics 2018-04-01
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