Chen Hung-Cheng, Hsu Chao-Ping, Reek Joost N H, Williams René M, Brouwer Albert M
Van 't Hoff Institute for Molecular Sciences, University of Amsterdam, P.O. Box 94157, 1090, GD, Amsterdam, The Netherlands.
Institute of Chemistry, Academia Sinica, 128 Section 2 Academia Road, Nankang, Taipei, 11529, Taiwan.
ChemSusChem. 2015 Nov;8(21):3639-50. doi: 10.1002/cssc.201500950. Epub 2015 Sep 23.
A series of new benzo[ghi]perylenetriimide (BPTI) derivatives has been synthesized and characterized. These remarkably soluble BPTI derivatives show strong optical absorption in the range of λ=300-500 nm and have a high triplet-state energy of 1.67 eV. A cyanophenyl substituent renders BPTI such a strong electron acceptor (Ered =-0.11 V vs. the normal hydrogen electrode) that electron-trapping reactions with O2 and H2 O do not occur. The BPTI radical anion on a fluorine-doped tin oxide|TiO2 electrode is persistent up to tens of seconds (t1/2 =39 s) in air-saturated buffer solution. As a result of favorable packing, theoretical electron mobilities (10(-2) ∼10(-1) cm(2) V(-1) s(-1)) are high and similar to the experimental values observed for perylene diimide and C60 derivatives. Our studies show the potential of the cyanophenyl-modified BPTI compounds as electron acceptors in devices for artificial photosynthesis in water splitting that are also very promising nonfullerene electron-transport materials for organic solar cells.
合成并表征了一系列新型苯并[ghi]苝四酰亚胺(BPTI)衍生物。这些具有显著溶解性的BPTI衍生物在λ=300 - 500 nm范围内表现出强烈的光吸收,并且具有1.67 eV的高三重态能量。氰基苯基取代基使BPTI成为如此强的电子受体(相对于标准氢电极,Ered = -0.11 V),以至于与O2和H2O的电子俘获反应不会发生。在空气饱和的缓冲溶液中,氟掺杂氧化锡|TiO2电极上的BPTI自由基阴离子可持续长达数十秒(t1/2 = 39 s)。由于有利的堆积,理论电子迁移率(10(-2) ∼10(-1) cm(2) V(-1) s(-1))很高,并且与苝二酰亚胺和C60衍生物观察到的实验值相似。我们的研究表明,氰基苯基修饰的BPTI化合物作为水分解人工光合作用器件中的电子受体具有潜力,同时也是用于有机太阳能电池的非常有前景的非富勒烯电子传输材料。