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Transparent Hole-Transporting Frameworks: A Unique Strategy to Design High-Performance Semitransparent Organic Photovoltaics
(1970-01-01)
Cheng, Pei
;
Wang, Hao-Cheng
;
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.
Enabling High-Performance Tandem Organic Photovoltaic Cells by Balancing the Front and Rear Subcells
(1970-01-01)
Cheng, Pei
;
Wang, Hao-Cheng
;
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%.
Engineering the Core Units of Small-Molecule Acceptors to Enhance the Performance of Organic Photovoltaics
(1970-01-01)
Wang, Hao-Cheng
;
Chen, Chung-Hao
;
Li, Ren-Hao
;
Lin, Yu-Che
;
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.
High-Efficiency Organic Tandem Solar Cells With Effective Transition Metal Chelates Interconnecting Layer
(2017-10-01)
Chang, Sheng-Yung
;
Lin, Yu-Che
;
Sun, Pengyu
;
Hsieh, Yao-Tsung
;
Meng, Lei
Organic tandem solar cells have two sub-cells vertically connected via a tunnel junction (or interconnecting layer, ICL), which the ICL plays a critical role of determining the performance of the tandem cell. In this manuscript, we report a new design of the ICL consisting of zirconium (IV) acetylacetonate (Zr-Acac) as the electron transport layer. The Zr-Acac has a suitable work function to pin the Fermi-level of the ICL and hence, can effectively behave as the charge recombination function for the tandem device. Comparing to the reference device consisting of ZnO ETL layer, the Zr-Acac ICL can effectively enhance the efficiency by 20%, from 8.4 to 10.1% power conversion efficiencies. More importantly, the Zr-Acac ETL layer functions effectively without thermal annealing, which not only simplifies the tandem solar cell processing, but also widens the front sub-cell material selection.
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.
Potassium-Presenting Zinc Oxide Surfaces Induce Vertical Phase Separation in Fullerene-Free Organic Photovoltaics
(2020-01-01)
Cheng, Hao-Wen
;
Raghunath, Putikam
;
Wang, Kai-li
;
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.
Trusted Worthy Fog Computing Testbed Developed in Great China Region
(2017-01-01)
Huang, ChingYao
;
Zao, John
;
Huang, Chih-Yuan
;
Kha Tho Nguyen
;
Yang, Yang
Fog computing has been widely adopted to meet the performance of explosive growth of IoT applications. In both 5G and IoT applications, low latency and ultra-reliable communication are two key features which cloud-based only architecture cannot meet those performance requirements. Fog computing which adds a hierarchy of elements between the cloud and endpoint devices can meet those requirements in a secure, high performance, open, and interoperable way. To validate whether future fog node products can meet trusted computing criteria and performance requirements or not, a common testbed is necessary. In this paper, we will first discussion the security practice (the fundamental pillar of OpenFog architecture) required for future testbed designs. National Chiao Tung University (NCTU) is leading to attempt to provide Security-as-a-Service (SECaaS) in NCTU testbed based on 4G wireless networks and two other fog enabled testbeds provided by ITRI's smart lamp posts testbed and Shanghai Tech's software defined (SD) LTE fog nodes testbed are also discussed for rapid prototyping of vertical industry applications. Two use cases, indoor autonomous vehicle and BATS codes multihop wireless will also be presented as the potential examples for testbeds.
Fog as a Service Technology
(2018-11-01)
Chen, Nanxi
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Yang, Yang
;
Zhang, Tao
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Zhou, Ming-Tuo
;
Luo, Xiliang
Fog computing has emerged as a promising solution for the loT and next generation mobile networks. As an extension to cloud computing, it enables service provisioning along the continuum from the cloud to things to reduce latency and bandwidth demands, and empower end users in their vicinity. Such a cloud-to-thing service continuum requires full technology support in infrastructure, platform, software and service levels. This article proposes FA(2)ST and its architecture to underpin a multi-level system of fog computing services for end-to-end support of loT applications. It presents the concept of FA(2)ST and describes its architecture, main features, a use case in a vertical industry, and a performance study.

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