Because the visible and the infrared (IR) regions take up ∼47% and ∼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. IRabsorbing 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 ∼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.
Recently, a new type of active layer with a ternary system has been developed to further enhance the performance of binary system organic photovoltaics (OPV). In the ternary OPV, almost all active layers are formed by simple ternary blend in solution, which eventually leads to the disordered bulk heterojunction (BHJ) structure after a spin-coating process. There are two main restrictions in this disordered BHJ structure to obtain higher performance OPV. One is the isolated second donor or acceptor domains. The other is the invalid metal-semiconductor contact. Herein, the concept and design of donor/acceptor/acceptor ternary OPV with more controlled structure (C-ternary) is reported. The C-ternary OPV is fabricated by a sequential solution process, in which the second acceptor and donor/acceptor binary blend are sequentially spin-coated. After the device optimization, the power conversion efficiencies (PCEs) of all OPV with C-ternary are enhanced by 14-21% relative to those with the simple ternary blend; the best PCEs are 10.7 and 11.0% for fullerene-based and fullerene-free solar cells, respectively. Moreover, the averaged PCE value of 10.4% for fullerene-free solar cell measured in this study is in great agreement with the certified one of 10.32% obtained from Newport Corporation.
Incorporating narrow-bandgap near-infrared absorbers as the third component in a donor/acceptor binary blend is a new strategy to improve the power conversion efficiency (PCE) of organic photovoltaics (OPV). However, there are two main restrictions: potential charge recombination in the narrow-gap material and miscompatibility between each component. The optimized design is to employ a third component (structurally similar to the donor or acceptor) with a lowest unoccupied molecular orbital (LUMO) energy level similar to the acceptor and a highest occupied molecular orbital (HOMO) energy level similar to the donor. In this design, enhanced absorption of the active layer and enhanced charge transfer can be realized without breaking the optimized morphology of the active layer. Herein, in order to realize this design, two new narrow-bandgap nonfullerene acceptors with suitable energy levels and chemical structures are designed, synthesized, and employed as the third component in the donor/acceptor binary blend, which boosts the PCE of OPV to 11.6%.
A simple strategy to balance the voltage-current trade-off in tandem organic photovoltaics by employing mixed non-fullerene acceptors in rear sub-cells is reported. The tandem device with the best power conversion efficiency (PCE) of 13.3% was achieved in the lab. Importantly, the tandem devices were certified by the National Renewable Energy Laboratory (NREL) under the new protocols (asymptotic scans, which are much tougher than regular fast scans); a PCE of 11.52% was achieved and recognized on the most recent NREL chart.
SUMMARYIn yeast, eIF5A, in combination with eEF2, functions at the translation step, during the protein elongation cycle. This result is of significance with respect to functioning of the enucleate sieve tube system, as eIF5A was recently detected in Cucurbita maxima (pumpkin) phloem sap. In the present study, we further characterized four CmeIF5A isoforms, encoding three proteins, all of which were present in the phloem sap. Although hypusination of CmeIF5A was not necessary for entry into the sieve elements, this unique post-translational modification was necessary for RNA binding. The two enzymes required for hypusination were detected in pumpkin phloem sap, where presumably this modification takes place. A combination of gel-filtration chromatography and protein overlay assays demonstrated that, as in yeast, CmeIF5A interacts with phloem proteins, like eEF2, known to be involved in protein synthesis. These findings are discussed in terms of a potential role for eIF5A in regulating protein synthesis within the enucleate sieve tube system of the angiosperms.
Semitransparent organic photovoltaics (ST‐OPVs) have great potential for use in renewable energy technologies. In bulk‐heterojunction (BHJ) ST‐OPVs, a compromise is necessary between the visible light transmittance (VLT) and the power conversion efficiency (PCE). A sequential deposition (SD) strategy that involves individually depositing a polymer donor layer (D) and a small‐molecule acceptor layer (A) as the active layer is presented; where molecular diffusion occurring at the interfacial region results in a pseudo p–i–n structure. PBDB‐T‐2F(D)/Y6(A) ST‐OPVs are fabricated with different active layer thicknesses—at 115 nm, the SD (D:A/75:40 nm) and BHJ devices (D:A/1:1.2 w) provide the champion PCE of 12.91% (VLT of 14.5%) and 12.77% (VLT of 13.4%), respectively; at 85 nm, the SD (D:A/45:40 nm) and BHJ devices (D:A/1:1.2 w) provide a PCE of 12.22% (VLT of 22.2%) and 11.23% (VLT of 16.6%), respectively. This trend indicates SD devices have larger PCE and VLT values than the BHJ devices at a given active layer thickness, and the enhancements of PCE and VLT values by the SD structures against the BHJ structures become more pronounced as the active layer thickness reduced. The SD strategy provides a new approach for achieving ST‐OPVs with both high efficiency and high transparency.
Polymer acceptors with acceptor-donor-acceptor (A-D-A) building blocks have demonstrated great potential in reaching excellent power conversion efficiency (PCE) and stability in the field of organic solar cells (OSCs), yet most...
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.
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