Browsing by Author "Huang, Kuo-Hsiu"

Now showing 1 - 3 of 3

2-Dimensional cross-shaped tetrathienonaphthalene-based ladder-type acceptor for high-efficiency organic solar cells
(2020-06-28)
Chang, Shao-Ling
;
Cao, Fong-Yi
;
Huang, Kuo-Hsiu
;
Lee, Wei-Liang
;
Lee, Meng-Hsun
AnNC-FICnonfullerene acceptor, using a didodecylnaphthodithiophene (NDT) embedded octacyclic ladder-type donorNC, had been described previously. In this work, a new cross-shapedTC-FICnonfullerene acceptor is designed by substitution of the NDT unit in theNCskeleton with a 2-dimensional didodecyltetrathienonaphthalene (TTN) unit. The 2-dimensionalTC pi-system with two vertically fused thiophenes strengthens the electron-donating ability, promotes pi-electron delocalization and enhances intramolecular donor-acceptor charge transfer and intermolecular pi-pi interactions. As a result,TC-FICshows more red-shifted and widened absorption compared to theNC-FICcounterpart. The PBDB-T:TC-FICdevice exhibits a higher efficiency of 11.6% which greatly outperformed the corresponding PBDB-T:NC-FICdevice with an efficiency of 7.52%. The dramatic 54% enhancement in efficiency is ascribed to the improved light-harvesting ability and enhanced charge mobilities which are benefited from the central 2-dimensionalTTNmoiety. By incorporatingPC(71)BMto improve absorption and electron transport, the ternary-blend PBDB-T : TC-FIC : PC(71)BMdevice (1 : 1 : 1 in wt%) achieves a highest PCE of 13.49% with an enhancedJ(sc)of 23.80 mA cm(-2), an FF of 64.4%, and aV(oc)of 0.88 V.
Isomerically Pure Benzothiophene-Incorporated Acceptor: Achieving Improved V-oc and J(sc) of Nonfullerene Organic Solar Cells via End Group Manipulation
(2019-09-11)
Chang, Shao-Ling
;
Hung, Kai-En
;
Cao, Fong-Yi
;
Huang, Kuo-Hsiu
;
Hsu, Chain-Shu
Benzene-based 1,1-dicyanomethylene-3-indanone (IC) derivatives have been widely utilized as the end-group to construct acceptor-donor-acceptor type nonfullerene acceptors (A-D-A type NFAs). The extension of the end-group conjugation of nonfullerene acceptors (NFAs) is a rational strategy to facilitate intermolecular stacking of the end-groups which are responsible for efficient electron transportation. A bicyclic benzothiophene-based end-group acceptor, 2-(3-oxo-2,3-dihydro-1H-benzo[b]cyclopenta[d]thiophen-1-ylidene)malononitrile, denoted as alpha-BC was designed and synthesized. The Knoevenagel condensation of the unsymmetrical 1,3-diketo-precursor with one equivalent of malononitrile selectively reacts with the keto group attached at the alpha-position of the thiophene unit, leading to the isomerically pure benzothiophene-fused alpha-BC. The well-defined alpha-BC with extended conjugation was condensed with three different ladder-type diformylated donors to form three new A-D-A NFAs named BDCPDT-BC, DTCC-BC, and ITBC, respectively. The corresponding IC-based BDCPDT-IC, DTCC-IC, and ITIC model compounds were also synthesized for comparison. The incorporation of the electron-rich benzothiophene unit in the end-group upshifts the lowest unoccupied molecular orbital energy levels of the NFAs, which beneficially enlarges the V-oc values. On the other hand, the benzothiophene unit in alpha-BC not also imparts an optical transition in the shorter wavelengths around 340-400 nm for a better light harvesting ability but also promotes the antiparallel pi-pi stacking of the end-groups for efficient electron transport. The organic photovoltaic cell devices using a PBDB-T polymer and BC-based NFAs all showed the improved V-oc and J(sc) values. The BDCPDT-BC- and DTCC-BC-based devices exhibited a power conversion efficiency (PCE) of 10.82 and 10.74%, respectively, which outperformed the corresponding BDCPDT-IC-, and DTCC-IC-based devices (9.33 and 9.25%). More importantly, the ITBC-based device delivered the highest PCE of 12.07% with a J(sc) of 19.90 mA/cm(2), a V-oc of 0.94 V, and an fill factor of 64.51%, representing a 14% improvement relative to the traditional ITIC-based device (10.05%).
New Thieno[3,2-b]thiophene-Based Acceptor: Tuning Acceptor Strength of Ladder-Type N-Type Materials to Simultaneously Achieve Enhanced V-OC and J(SC) of Nonfullerene Solar Cells
(2018-07-01)
Chang, Shao-Ling
;
Cao, Fong-Yi
;
Huang, Wen-Chia
;
Huang, Po-Kai
;
Huang, Kuo-Hsiu
A new thieno[3,2-b]thiophene-incorporated acceptor TTC has been developed. The TTC acceptor was installed in a haptacyclic ladder-type core (BDCPDT) to furnish an n-type BDCPDT-TTC. The standard PBDB-T:BDCPDT-IC device showed a PCE of 9.33% with a V-OC of 0.86 V and a J(SC) of 16.56 mA/cm(2). By molecular engineering of the acceptor unit, the BDCPDT:PBDB-T-based device delivered an enhanced efficiency of 10.29% with a simultaneously enhanced V-OC of 0.94 V and J(SC) of 17.72 mA/cm(2). Incorporation of the electron-donating thieno[3,2-b]thiophene unit into the acceptor moiety decreases the electron accepting strength, thereby upshifting the HOMO/LUMO energy levels to decrease the Delta E-HOMO and E-LOSS achieving a larger Voc. Second, the extended conjugated bicyclic thieno[3,2-b]thiophene ring beneficially induces an additional optical transition at short wavelengths, leading to improvement of J. Alternatively, BDCPDT-FIC installed with the fluorinated acceptor shows more red-shifted absorption to achieve a high J of 19.12 mA/cm(2).