Browsing by Author "Wang, Hao-Cheng"

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An universal electron transport layer involving hydrogen plasma-treated tungsten disulfide nanosheets doped zinc oxide layers for polymer donors with fullerene or small molecule acceptor photovoltaics
(2019-09-01)
Huang, Yi-Jiun
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Yen, Po-Jen
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Wang, Hao-Cheng
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Chen, Hsiu-Cheng
;
Wei, Kung-Hwa
A new universal electron transport layer that involves doping hydrogen-plasma-treated tungsten disulfide (WS2) nanosheets into ZnO for polymer/fullerene or small molecule organic photovoltaics (OPVs) was prepared. A hydrogen plasma treatment was used to alter the structures of WS2 nanosheets such that the W6+ content was converted into W4+; then ZnO:WS2 nanosheets composites were prepared to form electron transport layers (ETLs). The energy band of the ZnO:WS2 films could be tuned from 5.15 to 4.60 eV by varying the concentration of the WS2 nanosheets up to 0.5 wt%. It was found that ZnO:WS2 ETLs exhibited superior charge transport properties than those of the pristine ZnO layer because of the structure changes, as determined from the X-ray scattering characterizations. OPVs incorporating active layers of PTB7-TH/PC71BM and PTB7-TH/IDIC blends exhibited their power conversion efficiencies of 10.3% and 6.7%, respectively, with the incorporation of 0.3 wt% of the WS2 nanosheets, up from 8.9% to 5.4% for the corresponding devices featuring pristine ZnO-relative increases of 16% and 24%, respectively. This study demonstrates the effectiveness of hydrogen plasma treatment for altering the surface structures of two-dimensional transition-metal-dichalcogenide nanosheets, and paves a way for the composite electron transport layers for use in organic photovoltaics.
Dual nanocomposite carrier transport layers enhance the efficiency of planar perovskite photovoltaics
(2018-01-01)
Lin, Hsi-Kuei
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Li, Jia-Xing
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Wang, Hao-Cheng
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Su, Yu-Wei
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Wu, Kaung-Hsiung
In photovoltaic devices, more effective transfer of dissociated electrons and holes from the active layer to the respective electrodes will result in higher fill factors and short-circuit current densities and, thus, enhanced power conversion efficiencies (PCEs). Planar perovskite photovoltaics feature an active layer that can provide a large exciton diffusion length, reaching several micrometers, but require efficient carrier transport layers for charge extraction. In this study, we employed two nanocomposite carrier transfer layersan electron transport layer (ETL) comprising [6,6]phenyl-C-61-butyric acid methyl ester (PC61BM) doped with the small molecule 4,7-diphenyl-1,10-phenanthroline (Bphen), to enhance the electron mobility, and a hole transfer layer (HTL) comprising poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT:PSS) doped with molybdenum disulfide (MoS2) nanosheets, to enhance the hole mobility. We used ultraviolet photoelectron spectroscopy to determine the energy levels of these composite ETLs and HTLs; atomic force microscopy and scanning electron microscopy to probe their surface structures; and transmission electron microscopy and synchrotron grazing-incidence small-angle X-ray scattering to decipher the structures of the ETLs. Adding a small amount (less than 1%) of Bphen allowed us to tune the energy levels of the ETL and decrease the size of the PC61BM clusters and, therefore, generate more PC61BM aggregation domains to provide more pathways for electron transport, leading to enhanced PCEs of the resulting perovskite devices. We used quantitative pump-probe data to resolve the carrier dynamics from the perovskite to the ETL and HTL, and observed a smaller possibility of carrier recombination and a shorter injection lifetime in the perovskite solar cell doubly modified with carrier transport layers, resulting in an enhancement of the PCE. The PCE reached 16% for a planar inverted perovskite device featuring an ETL incorporating 0.5 wt% Bphen within PC61BM and 0.1 wt% MoS2 within PEDOT:PSS; this PCE is more than 50% higher than the value of 10.2% for the corresponding control device.
Enabling High-Performance Tandem Organic Photovoltaic Cells by Balancing the Front and Rear Subcells
(1970-01-01)
Cheng, Pei
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Wang, Hao-Cheng
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Zheng, Ran
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Zhu, Yuan
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Dai, Shuixing
In tandem organic photovoltaics, the front subcell is based on large-bandgap materials, whereas the case of the rear subcell is more complicated. The rear subcell is generally composed of a narrow-bandgap acceptor for infrared absorption but a large-bandgap donor to realize a high open-circuit voltage. Unfortunately, most of the ultraviolet-visible part of the photons are absorbed by the front subcell; as a result, in the rear subcell, the number of excitons generated on large-bandgap donors will be reduced significantly. This reduces the (photo) conductivity and finally limits the hole-transporting property of the rear subcell. In this work, a simple and effective way is proposed to resolve this critical issue. To ensure sufficient photogenerated holes in the rear subcell, a small amount of an infrared-absorbing polymer donor as a third component is introduced, which provides a second hole-generation and transporting mechanism to minimize the aforementioned detrimental effects. Finally, the short-circuit current density of the two-terminal tandem organic photovoltaic is significantly enhanced from 10.3 to 11.7 mA cm(-2)(while retaining the open-circuit voltage and fill factor) to result in an enhanced power conversion efficiency of 15.1%.
Engineering the Core Units of Small-Molecule Acceptors to Enhance the Performance of Organic Photovoltaics
(1970-01-01)
Wang, Hao-Cheng
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Chen, Chung-Hao
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Li, Ren-Hao
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Lin, Yu-Che
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Tsao, Cheng-Si
Understanding the chemical structures of next-generation small molecules is a critical step for increasing the performance of organic photovoltaics (OPVs); an OPV's small molecule determines not only the extent of light absorption but also the morphology. Herein, four small molecules featuring different cores-indaceno dithiophene, dithienoindeno indaceno dithiophene (IDTT), substituted IDTT, and dithienothiophene-pyrrolobenzothiadiazole-denoted as ID-4Cl, IT-4Cl, m-ITIC-OR-4Cl, and Y7, respectively, are selected to form active layers with poly(quinoxaline) (PTQ10) and poly(benzodithiophene-4,8-dione) (PM6). The Y7 devices exhibit the best performance in both systems, with the power conversion efficiency (PCE) reaching 14.5%; in comparison, ID-4Cl device gives a PCE of 10.0% for blending with PTQ10 and a relative efficiency enhancement of 45%. The same trend occurs for the cases of PM6 blend devices. This enhancement is attributed to i) the improved short-circuit current density that is provided by the greater degree of conjugation in S, N-heteroarenes ladder-type fused-ring cores of Y7, ii) an induced face-on Y7 orientation and smaller domain sizes that result from the sp(2)-hybridized nitrogen side chain, and iii) smaller energy loss. This study reveals the importance of the core structure on the device performance and provides guidelines for the design of new materials for OPV technologies.
Enhancing performance of ternary blend photovoltaics by tuning the side chains of two-dimensional conjugated polymer
(2019-08-01)
Chen, Chung-Hao
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Lu, Yi-Ju
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Su, Yu-Wei
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Lin, Yu-Che
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Lin, Hsi-Kuei
We prepared the ternary blends active layer by incorporating a new two-dimensional donor-acceptor (D/A) conjugated polymer (BDTTBO) comprising benzo-dithiophene-thiophene-thiophene-benzo oxadiazole chemical units that has three different conjugated side chains bithiophene (BT), benzothiophene (BzT) and thienothiophene (TT) BDTTBO-BT, BDTTBO-BzT and BDTTBO-TT into poly (benzodithiophene-fluorothienothiophene) (PTB7-TH) and PC71BM as for organic photovoltaics (OPVs). We expected that incorporating these BDTTBO with different side chains into the blend of PTB7-TH and PC71BM not only can broaden the absorption of solar spectrum thereby increasing short-circuit current density but also tune the packing of PTB7-TH and the dispersion of PC71BM. In particular, we found that incorporating 10% of BDTTBO-BT to form the PTB7-TH:BDTTBO-BT:PC71BM ternary blend (active layer) device could improve the power conversion efficiency to 10.4% from 9.0% for the binary blend of PTB7-TH:PC71BM device-a relative increase of 15%. We examined the packing orientations of the PBDTTBO:PTB7-TH:PC71BM ternary blend films using synchrotron two-dimensional grazing-incidence wide-angle X-ray scattering, and found that the incorporation of 10% relatively higher crystallinity PBDTTBO-BT, PBDTTBO-BzT or PBDTTBO-TT not only altered the packing orientation of PTB7-TH substantially but also reduced PC71BM cluster size in the ternary blend system, as compared to that in the case of PTB7-TH with PC71BM binary blend, thereby providing more pathways for electrons and thus enhancing the carrier transport in the ternary blend, as evidenced by the carrier mobility.
Enhancing photovoltaic performance by tuning the domain sizes of a small-molecule acceptor by side-chain-engineered polymer donors
(2019-02-21)
Lin, Yu-Che
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Lu, Yi-Ju
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Tsao, Cheng-Si
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Saeki, Akinori
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Li, Jia-Xing
This paper reports two new fluorine-substituted polymer donors (BO2FC8, BO2FEH), with different side-chain architectures, and a new chlorine-substituted small-molecule acceptor (m-ITIC-OR-4Cl) that are capable of simultaneous charge and energy transfer as the binary blend active layer for organic photovoltaics. We first resolved the single-crystal structure of m-ITIC-OR-4Cl and then used simultaneous grazing-incidence wide-and small-angle X-ray scattering to decipher the multi-length-scale structures-such as the shape and size of aggregated domains and molecular orientation-of the blends of BO2FEH and BO2FC8 with m-ITIC-OR-4Cl. The linear side chains of BO2FC8 facilitated its packing and, thus, induced m-ITIC-OR-4Cl to form smaller disc-shaped aggregated domains (thickness: 2.9 nm) than its aggregate domain (thickness: 5.4 nm) in the blend of the branched BO2FEH. That is, the binary blend system of linear-side-chain BO2FC8 with m-ITIC-OR-4Cl featured larger interfacial areas and more pathways for charge transfer and transport, as evidenced by their carrier mobilities. The highest power conversion efficiency (PCE) of 11.0% was that for the BO2FC8: m-ITIC-OR-4Cl device, being consistent with the predicted PCE of 11.2% using machine learning based on random forest algorism; in comparison, the PCE of the BO2FEH:m-ITIC-OR-4Cl device was 6.4%. This study has not only provided insight into the photovoltaic performances of new polymer donor/small-molecule acceptor blends but has also, for the first time, deciphered the hierarchical morphologies-from molecule orientation to nano-domain shape and size-of such blend systems, linking the morphologies to the photovoltaic performances. The use of side-chain architectures suggests an approach for tuning the morphology of the polymer/small-molecule binary blend active layer for use in organic photovoltaics.
Hydrogen plasma-treated MoSe2 nanosheets enhance the efficiency and stability of organic photovoltaics
(2019-10-07)
Wang, Hao-Cheng
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Lin, Yu-Che
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Chen, Chung-Hao
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Huang, Chi-Hsien
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Chang, Bin
In this paper we report the effect on the power conversion efficiency (PCE) and stability of photovoltaic devices after incorporating hydrogenated two-dimensional (2D) MoSe2 nanosheets into the active layer of bulk heterojunction (BHJ) organic photovoltaics (OPV). The surface properties of 2D MoSe2 nanosheets largely affect their dispersion in the active layer blend and, thus, influence the carrier mobility, PCE, and stability of corresponding devices. We treated MoSe2 nanosheets with hydrogen plasma and investigated their influence on the polymer packing and fullerene domain size of the active layer. For the optimized devices incorporating 37.5 wt% of untreated MoSe2, we obtained a champion PCE of 9.82%, compared with the champion reference PCE of approximately 9%. After incorporating the hydrogen plasma-treated MoSe2 nanosheets, we achieved a champion PCE of 10.44%-a relative increase of 16% over that of the reference device prepared without MoSe2 nanosheets. This PCE is the one of the highest ever reported for OPVs incorporating 2D materials. We attribute this large enhancement to the enhanced exciton generation and dissociation at the MoSe2-fullerene interface and, consequently, the balanced charge carrier mobility. The device incorporating the MoSe2 nanosheets maintained 70% of its initial PCE after heat-treatment at 100 degrees C for 1 h; in contrast, the PCE of the reference device decreased to 60% of its initial value-a relative increase in stability of 17% after incorporating these nanosheets. We also incorporated MoSe2 nanosheets (both with and without treatment) into a polymer donor (PBDTTBO)/small molecule (IT-4F) acceptor system. The champion PCEs reached 7.85 and 8.13% for the devices incorporating the MoSe2 nanosheets with and without plasma treatment, respectively-relative increases of 8 and 12%, respectively, over that of the reference. These results should encourage a push toward the implementation of transition metal dichalcogenides to enhance the performances of BHJ OPVs.
Potassium-Presenting Zinc Oxide Surfaces Induce Vertical Phase Separation in Fullerene-Free Organic Photovoltaics
(2020-01-01)
Cheng, Hao-Wen
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Raghunath, Putikam
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Wang, Kai-li
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Cheng, Pei
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Haung, Tianyi
Bulk heterojunction (BHJ) structure based organic photovoltaics (OPVs) have recently showed great potential for achieving high power conversion efficiencies (PCEs). An ideal BHJ structure would feature large donor/acceptor interfacial areas for efficient exciton dissociation and gradient distributions with high donor and acceptor concentrations near the anode and cathode, respectively, for efficient charge extraction. However, the random mixing of donors and acceptors in the BHJ often suffers the severe charge recombination in the interface, resulting in poor charge extraction. Herein, we propose a new approach-treating the surface of the zinc oxide (ZnO) as an electron transport layer with potassium hydroxide-to induce vertical phase separation of an active layer incorporating the nonfullerene acceptor IT-4F. Density functional theory calculations suggested that the binding energy difference between IT-4F and the PBDB-T-2Cl, to the potassium (K)-presenting ZnO interface, is twice as strong as that for IT-4F and PBDB-T-2Cl to the untreated ZnO surface, such that it would induce more IT-4F moving toward the K-presenting ZnO interface than the untreated ZnO interface thermodynamically. Benefiting from efficient charge extraction, the best PCEs increased to 12.8% from 11.8% for PBDB-T-2Cl:IT-4F-based devices, to 12.6% from 11.6% for PBDB-T-2Cl:Y1-4F-based devices, to 13.5% from 12.2% for PBDB-T-2Cl:Y6-based devices, and to 15.7% from 15.1% for PM6:Y6-based devices.
Rational Tuning of Molecular Interaction and Energy Level Alignment Enables High-Performance Organic Photovoltaics
(1970-01-01)
Wang, Rui
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Yuan, Jun
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Han, Guangchao
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Huang, Tianyi
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Huang, Wenchao
The performance of organic photovoltaics (OPVs) has rapidly improved over the past years. Recent work in material design has primarily focused on developing near-infrared nonfullerene acceptors with broadening absorption that pair with commercialized donor polymers; in the meanwhile, the influence of the morphology of the blend film and the energy level alignment on the efficiency of charge separation needs to be synthetically considered. Herein, the selection rule of the donor/acceptor blend is demonstrated by rationally considering the molecular interaction and energy level alignment, and highly efficient OPV devices using both-fluorinated or both-nonfluorinated donor/acceptor blends are realized. With the enlarged absorption, ideal morphology, and efficient charge transfer, the devices based on the PBDB-T-F/Y1-4F blend and PBDB-T-F/Y6 exhibit champion power conversion efficiencies as high as 14.8% and 15.9%, respectively.
Transparent Hole-Transporting Frameworks: A Unique Strategy to Design High-Performance Semitransparent Organic Photovoltaics
(1970-01-01)
Cheng, Pei
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Wang, Hao-Cheng
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Zhu, Yuan
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Zheng, Ran
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Li, Tengfei
Thanks to the nature of molecular orbitals, the absorption spectra of organic semiconductors are not continuous like those in traditional inorganic semiconductors, which offers a unique application of organic photovoltaics (OPVs): semitransparent OPVs. Recently, the exciting progress of materials design has promoted the development of semitransparent OPVs. However, in the perspective of device engineering, almost all reported works reduce the thickness of back/reflected electrode to obtain high average visible transmittance (AVT), which is a trade-off between power conversion efficiency (PCE) and the transmittance of the whole solar spectrum (visible and infrared), and therefore limit the further development. Herein, a unique strategy of "transparent hole-transporting frameworks" is proposed. A hole-transporting large-bandgap polymer (poly[bis(4-phenyl)(2,4,6-trimethylphenyl)amine (PTAA)) is employed to partially replace polymer donors in the active layer of PBDB-T/Y1. PTAA is a p-type polymer with a large bandgap of 2.9 eV; the partial substitution of PBDB-T by PTAA reduces the absorption of the active layer only in the visible region, keeping the hole-transporting pathways as well as the optimized film morphology. As a result, semitransparent OPVs with PCEs of 12% and AVTs of 20% are achieved, both on rigid and flexible substrates. To demonstrate the generality, this strategy is also used in three different active layers.