Browsing by Author "Cheng, Pei"

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Efficient Tandem Organic Photovoltaics with Tunable Rear Sub-cells
(2019-02-20)
Cheng, Pei
;
Liu, Yuqiang
;
Chang, Sheng-Yung
;
Li, Tengfei
;
Sun, Pengyu
A tandem structure was invented to enhance photon utilization efficiency and reduce thermal loss. Considering the unique advantages of non-fullerene acceptors (NFAs), the combination of NFAs and the tandem concept shows great potential for organic photovoltaics (OPVs). Herein, a simple strategy to balance the voltage-current trade-off in tandem OPVs by employing mixed NFAs in rear sub-cells is reported. The V-OC and J(SC) of rear sub-cells can be tuned by using the blend of donor/NFA/NFA. This strategy offers an easy approach to balance the V-OC and J(SC) in tandem OPVs toward higher power conversion efficiency (PCE) without rational and careful synthesis of new materials. Tandem OPVs based on mixed NFAs in rear sub-cells exhibited the best PCE of 13.3% in the lab. Importantly, the tandem devices were certified by the National Renewable Energy Laboratory (NREL) under asymptotic scans, and a PCE of 11.52% was achieved and recognized on the most recent NREL chart.
Enabling High-Performance Tandem Organic Photovoltaic Cells by Balancing the Front and Rear Subcells
(1970-01-01)
Cheng, Pei
;
Wang, Hao-Cheng
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Zheng, Ran
;
Zhu, Yuan
;
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%.
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
;
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
;
Yuan, Jun
;
Han, Guangchao
;
Huang, Tianyi
;
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.
Realizing Efficient Charge/Energy Transfer and Charge Extraction in Fullerene-Free Organic Photovoltaics via a Versatile Third Component
(2019-08-01)
Cheng, Hao-Wen
;
Zhang, Huotian
;
Lin, Yu-Che
;
She, Nian-Zu
;
Wang, Rui
Solution-processed organic photovoltaics (OPVs) based on bulk-heterojunctions have gained significant attention to alleviate the increasing demend of fossil fuel in the past two decades. OPVs combined of a wide bandgap polymer donor and a narrow bandgap nonfullerene acceptor show potential to achieve high performance. However, there are still two reasons to limit the OPVs performance. One, although this combination can expand from the ultraviolet to the near-infrared region, the overall external quantum efficiency of the device suffers low values. The other one is the low open-circuit voltage (V-OC) of devices resulting from the relatively downshifted lowest unoccupied molecular orbital (LUMO) of the narrow bandgap. Herein, the approach to select and incorporate a versatile third component into the active layer is reported. A third component with a bandgap larger than that of the acceptor, and absorption spectra and LUMO levels lying within that of the donor and acceptor, is demonstrated to be effective to conquer these issues. As a result, the power conversion efficiencies (PCEs) are enhanced by the elevated short-circuit current and V-OC; the champion PCEs are 11.1% and 13.1% for PTB7-Th:IEICO-4F based and PBDB-T:Y1 based solar cells, respectively.
Transparent Hole-Transporting Frameworks: A Unique Strategy to Design High-Performance Semitransparent Organic Photovoltaics
(1970-01-01)
Cheng, Pei
;
Wang, Hao-Cheng
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Zhu, Yuan
;
Zheng, Ran
;
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.
Unraveling Sunlight by Transparent Organic Semiconductors toward Photovoltaic and Photosynthesis
(2019-02-01)
Liu, Yugiang
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Cheng, Pei
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Li, Tengfei
;
Wang, Rui
;
Li, Yaowen
Because the visible and the infrared (IR) regions take up similar to 47% and similar to 51% of the energy in the solar spectrum (AM 1.5G standard), respectively, utilizing the visible light for plant growth and the IR light for power generation is potentially extremely exciting. IR-absorbing organic semiconductors, with localized IR absorption and visible-light transmittance, would be promising materials for this purpose. Here, flexible transparent organic photovoltaics (TOPVs) based on IR-absorbing organic materials were proposed, which can be a simple, low-cost, and promising way to utilize the IR light for electricity generation, and the penetrated visible light will be utilized for photosynthesis in plants. A power-conversion efficiency of similar to 10% with an average visible transmittance of 34% was achieved for TOPV devices. Meanwhile, the side-by-side comparison showed that plants grown under the TOPVs filtered light, and those under normal sunlight yielded very similar results. These outcomes demonstrated the results from TOPV devices beyond simple photovoltaic applications.