2020
DOI: 10.1016/j.jechem.2019.07.005
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TTA as a potential hole transport layer for application in conventional polymer solar cells

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Cited by 11 publications
(7 citation statements)
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“…A 3,6,11,14-Tetramethoxyphenylamine-dibenzo[g,p]chrysene (MeOPhN-DBC) layer was incorporated between MoO 3 and active-layer P3HT:PC 61 BM-inverted OSCs, showing an enhanced PCE of 3.68%, attributed to improved J sc and FF, and reduced leakage current [ 376 ]. Liu et al reported a tetrathiafulvalene derivative with four carboxyl groups (TTA) as an HTL in OSCs (see Figure 20 a) [ 377 ]. This HTL displayed a well-matched energy level (see Figure 20 b) and an enhanced PCE of 9.09% in comparison with a PEDOT:PSS-based OSC (see Figure 20 c).…”
Section: Hole-transporting Materials As Htls In Oscsmentioning
confidence: 99%
See 1 more Smart Citation
“…A 3,6,11,14-Tetramethoxyphenylamine-dibenzo[g,p]chrysene (MeOPhN-DBC) layer was incorporated between MoO 3 and active-layer P3HT:PC 61 BM-inverted OSCs, showing an enhanced PCE of 3.68%, attributed to improved J sc and FF, and reduced leakage current [ 376 ]. Liu et al reported a tetrathiafulvalene derivative with four carboxyl groups (TTA) as an HTL in OSCs (see Figure 20 a) [ 377 ]. This HTL displayed a well-matched energy level (see Figure 20 b) and an enhanced PCE of 9.09% in comparison with a PEDOT:PSS-based OSC (see Figure 20 c).…”
Section: Hole-transporting Materials As Htls In Oscsmentioning
confidence: 99%
“… ( a ) Illustration of OSCs structure based on TTA, ( b ) energy level diagram of different layers, and ( c ) J-V curves of devices with TTA and PEDOT:PSS as HTLs. Adapted with permission from [ 377 ]. Copyright 2020, Elsevier.…”
Section: Figures Schemes and Tablesmentioning
confidence: 99%
“…21 Tetrabenzoic acid 1o also found application as a hole-transport layer in conventional polymer solar cells. 22 TTFTB-based MOFs are now one of most important classes of redox-active MOFs.…”
Section: Short Review Synthesismentioning
confidence: 99%
“…Solution-processed OSCs use a bulk heterojunction (BHJ) design of the solar absorber layer, which consists of a mixture of at least acceptor (A) and donor (D) polymer molecules. Buckminsterfullerene (C 60 ) molecule derivatives, such as PC 60 BM and PC 70 BM, are often used as an electron acceptors in thin-film organic solar cells (TFOSCs), whose success has been mainly hindered by their narrow optical absorption band and low tunable energy band structure. Thus, fullerene-based OSCs suffered from high energy loss and low external quantum efficiency (EQE) compared to other solar cell technologies. However, in recent years, the small-molecule non-fullerene acceptor (NFA)-based thin-film organic solar cell (TFOSC) made rapid progress in attaining a high power conversion efficiency (PCE) value, as depicted in Figure . It is evident that the PCE of TFOSCs has become more and more competitive in terms of solar energy conversion compared to other solar cell technologies.…”
Section: Introductionmentioning
confidence: 99%