Jun‐Hua Wan

ORCID: 0000-0003-4061-7403
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Molecular Junctions and Nanostructures
  • Conducting polymers and applications
  • Luminescence and Fluorescent Materials
  • Perovskite Materials and Applications
  • Organic Light-Emitting Diodes Research
  • Surface Chemistry and Catalysis
  • Fullerene Chemistry and Applications
  • Synthesis and Properties of Aromatic Compounds
  • Graphene research and applications
  • Molecular Sensors and Ion Detection
  • Surface and Thin Film Phenomena
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Force Microscopy Techniques and Applications
  • Diamond and Carbon-based Materials Research
  • Porphyrin and Phthalocyanine Chemistry
  • Supramolecular Self-Assembly in Materials
  • Photochromic and Fluorescence Chemistry
  • Thermal Radiation and Cooling Technologies
  • Historical and Linguistic Studies
  • Micro and Nano Robotics
  • Synthetic Organic Chemistry Methods
  • Aquaculture Nutrition and Growth
  • Solar-Powered Water Purification Methods

Hangzhou Normal University
2015-2024

Nanjing University of Posts and Telecommunications
2018-2024

Hangzhou Academy of Agricultural Sciences
2018-2021

The Synergetic Innovation Center for Advanced Materials
2018

Hangzhou Xixi hospital
2015

State Key Laboratory of Silicon Materials
2014

Zhejiang University
2014

Fudan University
2005-2007

Nanjing University
2006

National University of Singapore
2006

A PCE of 5.16% with a <italic>V</italic><sub>oc</sub> 1.14 V is achieved thermally stable P3HT : SF(DPPB)<sub>4</sub> solar cells.

10.1039/c5ee03481g article EN Energy & Environmental Science 2015-12-03

This work focuses on developing diketopyrrolopyrrole (DPP)‐based small molecular nonfullerene acceptors for bulk heterojunction (BHJ) organic solar cells. The materials, SF‐DPP s, have an X‐shaped geometry arising from four DPP units attached to a spirobifluorene (SF) center. spiro‐dimer of DPP‐fluorene‐DPP is highly twisted, which suppresses strong intermolecular aggregation. Branched 2‐ethylhexyl (EH), linear n ‐octyl (C8), and ‐dodecyl (C12) alkyl sides are chosen as substituents...

10.1002/adfm.201502413 article EN Advanced Functional Materials 2015-08-27

A donor–acceptor polymer with broad absorption from 300 to 1700 nm as a photothermal material toward highly efficient solar-driven water evaporation.

10.1039/d2ta07628d article EN Journal of Materials Chemistry A 2023-01-01

Electron-rich (donor) and electron-deficient (acceptor) units to construct donor–acceptor (D–A) conjugated macrocycles were investigated elucidate their interactions with fullerene. Triphenylamine 4,7-bisthienyl-2,1,3-benzothiadiazole alternately linked through acetylene, as the donor acceptor units, respectively, for pentagonal 3B2A hexagonal 4B2A macrocycles. As detected by scanning tunneling microscopy, both D–A found form an interesting concentration-controlled nanoporous monolayer on...

10.1021/acsnano.7b06961 article EN ACS Nano 2017-11-01

Two novel organogelators based on 2,3,4,5-tetraphenylsilole functionalized with long-chain alkoxydiacylamido platforms (1a and 1b) were synthesized. The silole derivatives induced gelation of only hydrocarbon solvents showed aggregation-induced emission (AIE) in the gel state, contrast to very weak solution. polarized optical microscopic (POM) field scanning electron microscopy (FE-SEM) studies exhibited that xerogels formed fibrous structures. Hydrogen bonding π-stacking interactions main...

10.1039/b925746b article EN Soft Matter 2010-01-01

Two novel solution-processable acceptor-donor-acceptor (A-D-A)-structured organic small molecules with diketopyrrolopyrrole (DPP) as terminal acceptor units and pentathiophene (PTA) or pyrrole-modified (NPTA) the central donor unit, namely, DPP2(PTA) DPP2(NPTA), were designed synthesized. We examined effects of changing bridging heteroatoms five-ring-fused thienoacene core identity from sulfur [DPP2(PTA)] to nitrogen [DPP2(NPTA)] in small-molecule material. Replacement atom a different...

10.1021/am5006223 article EN ACS Applied Materials & Interfaces 2014-04-01

A coronene-cored perylene diimide twisted tetramer was developed as an acceptor additive to increase the <italic>V</italic><sub>oc</sub> values of <bold>PM6</bold>:<bold>Y6</bold> blend-based OSCs.

10.1039/d0tc05691j article EN Journal of Materials Chemistry C 2021-01-01

Fullerenes have been recognized as good candidates for solid lubricants. In this study, the microscale superlubricity of fullerene derivatives was accomplished by construction regular host–guest assembly structures. Herein, structures were successfully constructed on a highly oriented pyrolytic graphite (HOPG) surface introducing macrocycles templates and explicitly revealed scanning tunneling microscopy (STM). Meanwhile, nanotribological properties assemblies measured using atomic force...

10.1021/acsami.0c02726 article EN ACS Applied Materials & Interfaces 2020-03-31

Abstract A series of linear 2,5‐tetraphenylsilole‐vinylene‐type polymers were successfully synthesized for the first time. The tetraphenylsilole moieties linked at their 2,5‐positions through a vinylene bridge with p ‐dialkoxybenzenes to obtain polymer PSVB and 3,6‐carbazole PSVC . For comparison, 2,5‐tetraphenylsilole‐ethyne‐type PSEB was also synthesized, in which replaced an ethyne bridge. Very interestingly, bridging group (vinylene or ethyne) had significant effect on photophysical...

10.1002/asia.201200070 article EN Chemistry - An Asian Journal 2012-04-23

We have designed and synthesized one molecular building block, an aromatic trialdehyde derivative with three aldehyde groups, to form a potentially active structure. The scanning tunneling microscopy (STM) images show that the forms lamellar structures. By addition of reactant, 5-aminoisophthalic acid, it is found structure adlayer can be transformed from hexagonal as was expected. structural formation networks attributed condensation reaction between amine. Density functional theory (DFT)...

10.1021/jp1097876 article EN The Journal of Physical Chemistry C 2011-03-23

The optoelectronic properties of the cruciform p–n diblock oligomers 1–3 can be independently tuned by oligofluorene and oxadiazole branches to increase charge mobility.

10.1039/b517067b article EN New Journal of Chemistry 2006-01-01

We present a method for the modification of structure thieno[3,4-c]pyrrole-4,6-dione (TPD) to gain two novel acceptors TPN and TIN. And series donor–acceptor–donor-type oligomers 3TTPD3T, 3TTPN3T, 3TTIN3T, based on TPD, TIN, have been designed synthesized solution-processed small-molecule bulk-heterojunction (BHJ) solar cells. The impact these different central acceptor moieties their optical, electrochemical properties, morphology, cell performance were studied. Optical data showed that...

10.1039/c3ta10471k article EN Journal of Materials Chemistry A 2013-01-01

The pyrene core and significantly reduced intramolecular steric hindrance endow a nonfused PDI-tetramer with moderate planarity good self-assembly properties.

10.1039/c9tc02013f article EN Journal of Materials Chemistry C 2019-01-01

We report herein a series of macrocycles in which the densely π-stacked charge-transfer (CT) donor/acceptor with naphthalenediimides (NDIs) or perylene diimide (PDI) as acceptor moiety pairing various donor moieties are locked by covalent bond. The X-ray crystallography C8BDT-NDI reveals short intramolecular π-stacking distance around 3.4 Å and existence intermolecular (3.7 Å). CT is highly dependent on electron-donating ability replacing carbazole (C8KZ) benzo[1,2-b:4,5-b']dithiophene...

10.1002/anie.202413295 article EN Angewandte Chemie International Edition 2024-10-07

Abstract A six-membered chelated iridium complex containing aza-aromatic ligand is prepared. Emission color tuning from yellow to deep red observed for electroluminescent devices with different doping concentrations.

10.1246/cl.2005.1668 article EN Chemistry Letters 2005-11-19

A novel series of ladder π-conjugated materials--sila-pentathienoacenes (Si-PTA) are synthesized and characterized. Crystal structures the compounds show that length alkyl chains substituting on thiophene ring has a significant influence molecular packing. densely packed structure with an interfacial distance about 3.66 Å between adjacent molecules is observed for compound shorter chains. However, large (7.99 Å) obtained another because insertion long two planes. The investigation optical...

10.1002/asia.201000287 article EN Chemistry - An Asian Journal 2010-07-28

Abstract The cross‐shaped p–n diblock oligomers based on oligothiophenes (OTs) and 1,3,4‐oxadiazole (OXD) were synthesized investigated regarding optical properties, electrochemistry, quantum chemical calculations, intramolecular energy transfer. Since only one emission peak is observed in PL spectra of the oligomers, it evidenced that effective transfer from OXD to OTs branch. electrochemical experiments show almost complete spatial separation HOMO LUMO with thiophene number increasing....

10.1002/pola.21864 article EN Journal of Polymer Science Part A Polymer Chemistry 2007-02-04

A series of new ladder π-conjugated materials, phosphole modified pentathienoacene (PO-PTA), are synthesized and characterized. Single-crystal X-ray results demonstrate that methyl-disubstituted PO-PTA forms a face-to-face dimer structure driven by π–π interactions. The investigations optical properties showed the oxidized moiety in this system can effectively narrow band gap. is promising building block polymers oligomers for optoelectronic applications. derivative PO-PTA, obtained...

10.1039/c1ob06584j article EN Organic & Biomolecular Chemistry 2011-11-22
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