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1.
Chem Commun (Camb) ; 56(10): 1601-1604, 2020 Feb 04.
Article in English | MEDLINE | ID: mdl-31938789

ABSTRACT

Organic conjugated porous polymers, triazine-Ph-CPP and triazine-Th-CPP, are synthesized and characterized. Without further addition of co-catalysts, triazine-Ph-CPP exhibits a HER of 16 287 µmol g-1 h-1 and an apparent quantum yield of 61.5% at 365 nm, which demonstrates that the dibenzo[b,d]thiophene sulfone and 1,3,5-triazine based polymer is a unique prototype of a highly efficient hydrogen evolution photocatalyst.

2.
Chem Commun (Camb) ; 55(44): 6253-6256, 2019 May 28.
Article in English | MEDLINE | ID: mdl-31086923

ABSTRACT

The novel dicyanomethylene-substituted 1,2-bis(thieno[3,2-b]thiophene-2-yl)ethene based quinoidal compounds QBTTE and F2-QBTTE are reported. The FH (vinylene) hydrogen bonds lock the backbone conformation and greatly improve the transistor performance of F2-QBTTE.

3.
ACS Omega ; 3(8): 9290-9295, 2018 Aug 31.
Article in English | MEDLINE | ID: mdl-31459061

ABSTRACT

Due to their strong intermolecular interactions, polymer semiconductors aggregate in solution even at elevated temperature. With the aim to study the effect of this kind preaggregation on the order of thin films and further transistor performance, bi-thieno[3,4-c]pyrrole-4,6-dione and fluorinated oligothiophene copolymerized polymer semiconductor P1, which shows strong temperature-dependent aggregation behavior in solution, is synthesized. Its films are deposited through a temperature-controlled dip-coating technique. X-ray diffraction and atomic force microscopy results reveal that the aggregation behavior of P1 in solution affects the microstructures and order of P1 films. The charge transport properties of P1 films are investigated with bottom-gate top-contacted thin-film transistors. The variation of device performance (from 0.014  to 1.03 cm2 V-1 s-1) demonstrates the importance of optimizing preaggregation degree. The correlation between preaggregation degree and transistor performance of P1 films is explored.

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