Browsing by Author "Yang, Yang"

Now showing 1 - 20 of 21

A Metal-Oxide Interconnection Layer for Polymer Tandem Solar Cells with an Inverted Architecture
(2011-03-01)
Chou, Cheng-Hsuan
;
Kwan, Wei Lek
;
Hong, Ziruo
;
Chen, Li-Min
;
Yang, Yang
A metal-oxide-only interconnecting layer for application in inverted polymer tandem solar cells is reported. Good electrical and optical coupling of the two sub-cells is achieved by using a carefully designed MoO(3)/Al/ZnO layer, which leads to a power coversion efficiency of 5.1%. The results demonstrate that effective connection between polymer bulk heterojunctions can be realized by this facile metal-oxide interlayer.
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.
Electrohydrodynamic-assisted Assembly of Hierarchically Structured, 3D Crumpled Nanostructures for Efficient Solar Conversions
(2016-12-07)
Ishihara, Hidetaka
;
Chen, Yen-Chang
;
De Marco, Nicholas
;
Lin, Oliver
;
Huang, Chih-Meng
The tantalizing prospect of harnessing the unique properties of graphene crumpled nanostructures continues to fuel tremendous interest in energy storage and harvesting applications. However, the paper ball-like, hard texture, and closed-sphere morphology of current 3D graphitic nanostructure production not only constricts the conductive pathways but also limits the accessible surface area. Here, we report new insights into electrohydrodynamically-generated droplets as colloidal nanoreactors in that the stimuli-responsive nature of reduced graphene oxide can lead to the formation of crumpled nanostructures with a combination of open structures and doubly curved, saddle-shaped edges. In particular, the crumpled nanostructures dynamically adapt to non-spherical, polyhedral shapes under continuous deposition, ultimately assembling into foam-like microstructures with a highly accessible surface area and spatially interconnected transport pathways. The implementation of such crumpled nanostructures as three-dimensional rear contacts for solar conversion applications realize benefits of a high aspect ratio, electrically addressable and energetically favorable interfaces, and substantial enhancement of both short-circuit currents and fill-factors compared to those made of planar graphene counterparts. Further, the 3D crumpled nanostructures may shed lights onto the development of effective electrocatalytic electrodes due to their open structure that simultaneously allows for efficient water flow and hydrogen escape.
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%.
Energy transfer within small molecule/conjugated polymer blends enhances photovoltaic efficiency
(2017-09-14)
Lin, Yu-Che
;
Su, Yu-Wei
;
Li, Jia-Xing
;
Lin, Bo-Hsien
;
Chen, Chung-Hao
In this study, we employed ternary blends capable of energy transfer-a synthesized high-band-gap small molecule (SM-4OMe) comprising benzodithiophene (BDT) and rhodanine units (a molecular structure that was designed for energy transfer), a low-band-gap polymer (PTB7-TH) comprising BDT and thienothiophene units with desired packing orientation, and a fullerene-as active layers for singlejunction photovoltaic devices. The light absorption of the small molecule and the polymer was partially complementary, owing to their band gap difference, thereby broadening the absorption spectrum of solar light while maintaining the energy band structures that facilitated energy and charge transfer. The synthesized small molecule SM-4OMe and the PTB7-TH had somewhat similar chemical structureswith the same planar BDT donor units-and thus allowed sufficient mixing between them for energy transfer to take place. The power conversion efficiency of a device incorporating a ternary blend of PTB7-TH:SM-4OMe:PC71BM (0.9 :0.1 :1.5, w/w/w) as the active layer, processed with diiodooctane (2 vol%) in chlorobenzene, was 10.4%, which is higher than the value of 8% of the corresponding device incorporating PTB7-TH:PC71BM (1 :1.5, w/w)-an increase of 30%. We attribute this enhancement to the energy transfer from the high-band-gap small molecule SM-4OMe to the low-band-gap polymer PTB7-TH and to the optimal phase-separated bulk heterojunction morphology that comprises a mean PC71BM cluster size of 6 nm, which is lower than 12 nm for the PTB7-TH and PC71BM binary blends, and slightly better in-plane packing, arising from the inducements of the presence of SM-4OMe. This approach provides a facile and effective way to enhance the power conversion efficiency of single junction organic photovoltaics.
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.
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
;
Lu, Yi-Ju
;
Tsao, Cheng-Si
;
Saeki, Akinori
;
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.
Fog as a Service Technology
(2018-11-01)
Chen, Nanxi
;
Yang, Yang
;
Zhang, Tao
;
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.
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.
Molecular engineering of side chain architecture of conjugated polymers enhances performance of photovoltaics by tuning ternary blend structures
(2018-01-01)
Lin, Yu-Che
;
Cheng, Hao-Wen
;
Su, Yu-Wei
;
Lin, Bo-Hsien
;
Lu, Yi-Ju
Several approaches, including the use of small molecule acceptors, novel polymer structures, and tandem cell structures, have been adopted to prepare polymer solar cells displaying high power conversion efficiencies (PCEs). The application of ternary blends as the active layer for polymer solar cells-for which the absorption spectra can be tuned by varying the composition ratios of components-is another facile approach toward optimizing the PCEs of devices. The selection of suitable ternary blends active layer often relies on intuition and remains a formidable challenge. Here, we adopted a systemic approach of not only using the same donor chemical units in the two donor-acceptor (D/A) conjugated polymers with complementary light absorption (energy band gaps) but also varying the side chains architectures as a means of tuning the packing of these semi-planar conjugated polymers, thereby influencing the carrier transport and optimizing the PCE. We employed linear, branch and mixed linear-and-branch side-chain attached benzooxadiazole (BO) as the acceptor (A) units in poly [benzodithiophene-thiophene-benzooxadiazole] (PBDTTBO) conjugated polymers and monitored their interactions with poly[benzodithiophene-fluorothienothiophene] (PTB7-TH), both of which featured the same benzodithiophene (BDTT) donor (D) units. We found that incorporating a minor amount (10%) of D/A conjugated PBDTTBO with such side chains into the PTB7-TH with a fullerene allowed us to tune the packing of the two polymers and, thereby, enhance the PCEs of corresponding ternary blend devices; the PCE of the ternary blend device incorporating PBDTTBO with two branched-side chains, PTB7-TH, and PC71BM increased to 11.4% from 9.0% for the device incorporating only the binary blend of PTB7-TH and PC71BM-a relative increase of more than 25%. This approach of using side chain engineering to tune the structure of a minor conjugated polymer and, thus, influence the packing of another major conjugated polymer that features the same donor chemical units appears to be an effective means of preparing highly efficient polymer cells.
Numerical prediction of effective dielectric constant in organic thin-film transistors with nanocomposite gate insulator
(2005)
Chuang, Chiao-Shun
;
Shieh, Han-Ping D.
;
Yang, Yang
;
Chen, Fang-Chung
;
顯示科技研究所
High performance organic thin-film transistors (OTFTs) incorporated with nanoparticles in the dielectric insulators have been demonstrated. The dielectric layers consist of cross-linked poly-4- vinylphenol (PVP) and a high dielectric titanium dioxide (TiO(2)) nanoparticles. It was found that the OTFTs with the nanocomposite dielectric layers have higher field-induced current than that of convention devices because the dielectric constant of the gate insulator is higher. Several models are also propsed to derive the dielectric constants of the nanocomposition layers. The best fit model suggests that the dielectric constant increases exponentially with filler volume at high filler volume regions, which indicates this method is effective to enchance the output power of OTFTs.
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.
Special Issue on Fog Networks
(2018-06-01)
Yang, Yang
;
Yang, Xiumei
;
Song, Wenzhan
;
Zao, John K.
;
Chiang, Mung
The investigation of donor-acceptor compatibility in bulk-heterojunction polymer systems
(2013-07-22)
Huang, Jen-Hsien
;
Hsiao, Yu-Sheng
;
Richard, Eric
;
Chen, Chun-Chao
;
Chen, Peilin
The fullerene derivative, indene-C-60 bisadduct (ICBA), has been introduced into poly(3-hexylthiophene) (P3HT) to improve the efficiency of P3HT-based devices. However, we found that ICBA is not suitable for most low bandgap polymers. In this study, we have correlated the cell performance with surface energy between the donor and acceptor materials in a bulk-heterojunction cell. These results show that higher photocurrent can be attributed to the morphology improvement induced by larger surface energy difference (Delta gamma) between the low bandgap polymer and fullerene. These results also suggest that synthetic strategies which adjust the Delta gamma between donor and acceptor should be considered. (C) 2013 AIP Publishing LLC.
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.
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.
Unraveling Sunlight by Transparent Organic Semiconductors toward Photovoltaic and Photosynthesis
(2019-02-01)
Liu, Yugiang
;
Cheng, Pei
;
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.
Vertical Phase Separation in Poly(3-hexylthiophene): Fullerene Derivative Blends and its Advantage for Inverted Structure Solar Cells
(2009-04-23)
Xu, Zheng
;
Chen, Li-Min
;
Yang, Guanwen
;
Huang, Chun-Hao
;
Hou, Jianhui
A method which enables the investigation of the buried interfaces without altering the properties of the polymer films is used to study vertical phase separation of spin-coated poly(3-hexylthiophene) (P3HT):fullerene derivative blends. X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) analysis reveals the P3HT enrichment at the free (air) surfaces and abundance of fullerene derivatives at the organic/substrate interfaces. The vertical phase separation is attributed to the surface energy difference of the components and their interactions with the substrates. This inhomogeneous distribution of the donor and acceptor components significantly affects photovoltaic device performance and makes the inverted device structure a promising choice.