2009
DOI: 10.1039/b818693f
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Soluble n-type pentacene derivatives as novel acceptors for organic solar cells

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Cited by 104 publications
(81 citation statements)
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References 28 publications
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“…Although the structure could not be resolved fully, the ADT derivative appeared to adopt a "sandwich herringbone" motif similar to that observed in some pentacene-based photovoltaic acceptors. [19][20][21] In this motif, π -stacking interactions are strictly one-dimensional, and a high mobility is not expected, in agreement with the electrical measurements presented later. The TDT derivative consistently formed low-quality single crystals, likely due to the lower symmetry compared with ADT and PDT, and only a crude model of the structure was possible.…”
Section: Doi: 101002/adma201101619supporting
confidence: 83%
“…Although the structure could not be resolved fully, the ADT derivative appeared to adopt a "sandwich herringbone" motif similar to that observed in some pentacene-based photovoltaic acceptors. [19][20][21] In this motif, π -stacking interactions are strictly one-dimensional, and a high mobility is not expected, in agreement with the electrical measurements presented later. The TDT derivative consistently formed low-quality single crystals, likely due to the lower symmetry compared with ADT and PDT, and only a crude model of the structure was possible.…”
Section: Doi: 101002/adma201101619supporting
confidence: 83%
“…More recently, solution-processed solar cells using soluble organic small molecules have attracted great attention for their numerous attractive features such as high molecular purity, reproducibility and scalable synthesis, tunable optoelectronic properties through structural control and high carrier mobility [17,18]. Much efforts have been devoted to design electron-donating materials for improving efficiency of solar cells, while the search for the novel acceptors is quite limited [19][20][21][22]. To develop efficient acceptor for heterojunction solar cells, one of the available approaches is the introduction of some multiple functional groups with extended absorption and high absorption coefficient, which will lead to the new acceptor possessing the characteristics of solution-processed, high light-absorbing and well charge carrier transporting ability.…”
Section: Introductionmentioning
confidence: 99%
“…[26][27][28][29][30] For SMBHJs, of particular interest are solution-processable photoconductive organic semiconductors with high charge carrier mobilities and solid-state packing favoring efficient charge separation at the D/A interfaces. 31 Examples of such materials are functionalized pentacene (Pn) and anthradithiophene (ADT) derivatives which exhibit thin-film charge carrier (hole) mobilities of above $1.5 cm 2 /(Vs), fast photoresponse, high photoconductivity under continuous wave (cw) excitation, [32][33][34] and a variety of solid-state packing motifs controlled by functionalization of the molecules. 35 Investigation of mechanisms of charge photogeneration and transport in such materials and their D/A composites is the focus of this paper.…”
Section: Introductionmentioning
confidence: 99%