Bo Liu

ORCID: 0000-0003-0989-2191
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About
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Research Areas
  • Organic Electronics and Photovoltaics
  • Conducting polymers and applications
  • Organic Light-Emitting Diodes Research
  • Perovskite Materials and Applications
  • Molecular Junctions and Nanostructures
  • Semiconductor materials and interfaces
  • Electrochemical Analysis and Applications
  • Synthesis and Properties of Aromatic Compounds
  • Thin-Film Transistor Technologies
  • Luminescence and Fluorescent Materials
  • Carbon Nanotubes in Composites
  • Adsorption and biosorption for pollutant removal
  • Nanowire Synthesis and Applications
  • Surface Modification and Superhydrophobicity
  • Odor and Emission Control Technologies
  • Fullerene Chemistry and Applications
  • Polymer Surface Interaction Studies
  • Advanced Memory and Neural Computing
  • Extraction and Separation Processes
  • Analytical Chemistry and Sensors
  • Covalent Organic Framework Applications
  • Electrodeposition and Electroless Coatings
  • Advanced biosensing and bioanalysis techniques
  • Advanced Sensor and Energy Harvesting Materials
  • Polymer crystallization and properties

Qilu University of Technology
2024

Shandong Academy of Sciences
2024

Hunan University of Arts and Science
2020-2023

Guangdong University of Technology
2023

University of Chinese Academy of Sciences
2023

Hunan University of Science and Technology
2023

The First People's Hospital of Changde
2020-2021

Materials Science & Engineering
2021

Beijing National Laboratory for Molecular Sciences
2020

Institute of Chemistry
2020

Three new benzo[1,2-b:4,5-b′]difuran-based donor–acceptor conjugated polymers, namely poly{4,8-bis(2′-ethylhexyloxy)benzo[1,2-b;3,4-b′]difuran-alt-5,5-(4′,7′-di-2-thienyl-5′,6′-dioctyloxy-2′,1′,3′-benzothiadiazole)}(PBDFDODTBT), poly{4,8-bis(2′-ethylhexyloxy)benzo[1,2-b;3,4-b′]difuran-alt-5,5-(4′,7′-di-2-thienyl-2-octyl-2′,1′,3′-benzotriazole)}(PBDFDTBTz), poly{4,8-bis(2′-...

10.1021/ma301053q article EN Macromolecules 2012-08-27

Small molecule donor/polymer acceptor bulk-heterojunction films with both compounds strongly absorbing have great potential for further enhancement of the performance organic solar cells. By employing a newly synthesized small donor commercially available polymer in solution-processed fullerene-free system, high power conversion efficiency close to 4% is reported. As service our authors and readers, this journal provides supporting information supplied by authors. Such materials are peer...

10.1002/adma.201405485 article EN Advanced Materials 2015-02-02

Three low bandgap isoindigo-based conjugated polymers were synthesized. The polymer films exhibit broad absorption bands in the wavelength region from 300 nm to 810 nm. <bold>PBDTID</bold> exhibited relatively better photovoltaic properties with a PCE of up 0.9%.

10.1039/c0py00401d article EN Polymer Chemistry 2011-01-01

A new donor–acceptor type copolymer, namely poly{4,8-bis(2-ethylhexyloxy)benzo[1,2-b:3,4-b′]difuran-alt-6-octylnaphtho[2,3-c]thiophene-4,9-dione} (PBDFNTDO) was synthesized by a Stille coupling reaction and characterized 1H NMR, GPC, TGA, UV-Vis absorption spectroscopy cyclic voltammetry. PBDFNTDO is readily soluble in common organic solvents with number-average molecular weight (Mn) of 10.7 kDa mol−1 polydispersity index 1.71. TGA analysis shows the copolymer exhibits good thermal stability...

10.1039/c2jm32843g article EN Journal of Materials Chemistry 2012-01-01

Three new alkylthienyl substituted benzodithiophene (BDT)-based polymers, poly{4,8-bis(2′-ethylhexylthiophene)benzo[1,2-b;3,4-b′]dithiophene-alt-5,5-(4′,7′-di-2-thienyl-5′,6′-dioctyloxy-benzo[c][1,2,5]oxadiazole)}(PBDTTDTBO), poly{4,8-bis(2′-ethylhexylthiophene)benzo[1,2-b;3,4-b′]dithiophene-alt-5,5-(4′,7′-di-2-thienyl-5′,6′-dioctyloxy-2′,1′,3′-benzothiadiazole)}(PBDTTDTBT) and poly{4,8-bis(2′-ethyl...

10.1039/c2ta00474g article EN Journal of Materials Chemistry A 2012-10-16

Abstract A new dithienyl benzotriazole‐based conjugated polymer was synthesized by Suzuki coupling reaction. The found to be soluble in common organic solvents, such as chloroform, tetrahydrofuran and chlorobenzene, with excellent film‐forming properties. structure of the confirmed 1 H NMR, molecular weights determined GPC thermal properties investigated TGA DSC. films exhibited an absorption band wavelength range 300 610 nm. Preliminary photovoltaic cells based on composite indium tin oxide...

10.1002/macp.201000315 article EN Macromolecular Chemistry and Physics 2010-08-16

In this work, the quantitative relationship in heredity of β-phase from a solution to thin film based on poly(9,9-dioctylfluorene) (PFO), mechanism formation, and effects contents hole mobility were investigated. The PFO was characterized through UV–vis absorption. Results indicated that can be completely transferred solutions films during drying form films. stable could manage dynamic changes liquid state thin-film state. content higher diluted solutions, reason revealed light scattering....

10.1021/acs.jpcc.6b08941 article EN The Journal of Physical Chemistry C 2016-11-28

A new low bandgap conjugated polymer—PBDFTT-C was synthesized from thieno-[3,4-b]thiophene and benzo[1,2-b:4,5-b′]difuran units by Stille coupling reactions. The structure verified 1H NMR elemental analysis, the molecular weight determined gel permeation chromatography (GPC) thermal properties were investigated thermogravimetric analysis (TGA). PBDFTT-C showed a HOMO energy level of −5.27 eV. polymer film displayed broad absorption in wavelength region 300 nm to 840 with 1.48 field effect...

10.1039/c2py20580g article EN Polymer Chemistry 2012-09-12

The large current densities attained by carbon nanotube enabled vertical field effect transistors using crystalline organic channel materials are somewhat unexpected given the known anisotropy in mobility of organics and their conventional ordering on dielectric surfaces which tends to orient high axes parallel surface. This seeming contradiction is resolved finding that nanotubes induce a molecular reorients favor flow direction perpendicular substrate

10.1021/nn102721v article EN ACS Nano 2010-12-09

Abstract A new donor–acceptor type polyfluorene derivative, poly[9,9‐dioctyl‐2,7‐fluorene‐alt‐(4,7‐bis(2′‐thienyl)‐2‐octyl‐2,1,3‐benzotriazole)] (PFDTBTz), is synthesized by a Suzuki cross‐coupling polymerization reaction. The optical, electrochemical, photovoltaic, and electroluminescence properties of PFDTBTz are investigated in detail. maximum power conversion efficiency (PCE) the PSCs based on PFDTBTz/PC 71 BM (1:2 w/w) reaches 2.1% with short circuit current density ( J sc ) 5.73 mA ·...

10.1002/macp.201100080 article EN Macromolecular Chemistry and Physics 2011-05-12

Maximizing the power conversion efficiency of organic solar cells requires simultaneous optimization its short‐circuit current density, fill factor, and open‐circuit voltage V oc . Several key parameters device model needed to understand these quantities have not been reliably determined, even for prototypical poly(3‐hexylthiophene):phenyl‐C 61 ‐methylbutyric ester (P3HT:PCBM) photoactive layer (PAL). Detailed analysis loss mechanisms at contacts their rational possible. Here, using...

10.1002/aenm.201200972 article EN Advanced Energy Materials 2013-10-31

The effects of alkyl side-chain length with different carbon atom number, called poly(9,9di-hexlyfluorene) (PF6), poly(9,9-diheptylfluorene) (PF7), poly(9,9-dioctylfluorene) (PF8), poly(9,9-dinonylfluorene) (PF9), and poly(9,9-didecylfluorene) (PF10), on the polyfluorene (PF) single-chain conformation, β its stability chain aggregation in solution dynamic process were systematically investigated by dynamic/static light scattering, UV–vis absorption spectra, photoluminescence scanning...

10.1021/acs.jpcc.8b03504 article EN The Journal of Physical Chemistry C 2018-05-21

Two new D–A alternating copolymers, PBDFFBT and PBDTFBT, featuring a fluorinated benzothiazole (BT) electron-acceptor unit the electron-donor segments of benzo[1,2-b:4,5-b′]difuran (BDF) or benzo[1,2-b:4,5-b′]dithiophene (BDT), were prepared by standard Stille cross-coupling reaction. The resulting copolymers characterized TGA, GPC, UV-vis absorption spectroscopy cyclic voltammetry measurements. PBDTFBT show good film forming properties. Bulk heterojunction polymer photovoltaic devices based...

10.1039/c3ra41140k article EN RSC Advances 2013-01-01

A mutual transformation dynamic process and mechanism between the α-conformation β-conformation in PFO solution.

10.1039/c5sm00074b article EN Soft Matter 2015-01-01

A series of donor–acceptor (D–A) copolymers from a benzodithiophene (BDT) donor unit and naphtho[2,3-c]thiophene-4,9-dione (NTDO) acceptor with different side chains, PBDTNTDO-C1, PBDTNTDO-C2 PBDTNTDO-C3, were synthesized by standard Stille cross-coupling polymerization. The thermal, optical electrochemical properties the well investigated. Preliminary investigations based on device structure ITO/PEDOT : PSS/polymer: PC71BM (1 2)/Ca/Al showed power conversion efficiencies (PCEs) 1.96% for...

10.1039/c2ra20747h article EN RSC Advances 2012-01-01

A new building block of naphtho[1,2-b:5,6-b′]difuran (NDF) with alkyl chains was firstly designed and synthesized. NDF used as the electron donor unit in constructing a low band gap copolymer (PNDFDTBT). polymer solar cell configuration ITO/PEDOT:PSS/PNDFDTBT:PC71BM (1 : 2,w/w)/Ca/Al demonstrates promising power conversion efficiency (PCE) 4.5%.

10.1039/c3ra40268a article EN RSC Advances 2013-01-01

Abstract The interface between the organic semiconductor and dielectric plays an important role in determining device performance of field‐effect transistors (OFETs). Although self‐assembled monolayers (SAMs) made from organosilanes have been widely used for modification to improve OFETs, they suffer incontinuous lack uniform coverage layer. Here, it is reported that by introduction a solution‐processed organozinc compound as layer silane SAM, improved surface morphology reduced polarity can...

10.1002/adfm.201200316 article EN Advanced Functional Materials 2012-06-13
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