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Multiparameter Franck–Condon analyses of absorption spectra of Y6 in dilute solutions reveals that Y6 exhibits a high conformation uniformity and the smallest intra-molecular reorganization energy among the materials studied.

 

Flexible electronics have received considerable attention in the past decades due to their promising application in rollable display screens, wearable devices, implantable devices, and other electronic applications. In particular, conjugated polymers are favored for flexible electronics due to their mechanical flexibility and potential for solution‐processed fabrication techniques, such as blade‐coating, roll‐to‐roll printing, and high‐throughput printing allowing for high‐performance transistor devices. Thiophene is the prevailing conjugated unit to construct these conjugated polymers due to its favorable electronic properties. On the other hand, furans are among the few conjugated moieties that are easily derived from bio renewable resources. To promote sustainability, we selectively introduced furan into the conjugated backbone of a high‐mobility polymer scaffold and systematically studied the effect on the microstructure and charge transport. We show that partially and selectively replacing thiophene units with furan can yield nearly comparable performance compared to the all‐thiophene polymer. This strategy offers an improvement in the sustainability of the polymer by incorporating bio‐sourced furan without sacrificing the high‐performance characteristics. Meanwhile, polymers with incorrect or complete furan incorporation show reduced mobilities. This work serves to develop coherent structure–morphology–performance relationships; such knowledge will establish guidelines for the future development of sustainable, furan‐based conjugated materials.

 

Greenhouses conserve land and water while increasing crop production, making them an attractive system for low environmental impact agriculture. Yet, to achieve this goal, there is a need to reduce their large energy demand. Employing semitransparent organic solar cells (OSCs) on greenhouse structures provide an opportunity to offset the greenhouse energy needs while maintaining the lighting needs of the plants. However, the design trade-off involved in optimizing solar power generation and crop productivity to maximize greenhouse economic value is yet to be studied in detail. Here, a functional plant growth model is integrated with a dynamic energy model that includes supplemental lighting to optimize the economics of growing lettuce and tomato. The greenhouse optimization considers 64 different OSC active layers with varying roof coverage for 25 distinct climates providing a global perspective. We find that crop yield is the primary economic driver, and that crop yield can be maintained in OSC-greenhouses across diverse climates. The crop productivity along with the energy produced by the OSCs results in improved net present value of the OSC-greenhouses relative to conventional systems in most climates for both lettuce and tomato. In addition, we find common solar cell active layers that maximize greenhouse economic value resulting in guidelines for scaling up OSC-greenhouse design. Through this model framework, we highlight the opportunity for OSCs in greenhouses, uncover designs and locations that provide the most value, and provide a basis for further development of OSC-greenhouses to achieve a sustainable means of food production. 

Precise determination of structural organization of semi-conducting polymers is of paramount importance for the further development of these materials in organic electronic technologies. Yet, prior characterization of some of the best-performing materials for transistor and photovoltaic applications, which are based on polymers with rigid backbones, often resulted in conundrums in which X-ray scattering and microscopy yielded seemingly contradicting results. Here we solve the paradox by introducing a new structural model, i.e. , semi-paracrystalline organization. The model establishes that the microstructure of these materials relies on a dense array of small paracrystalline domains embedded in a more disordered matrix. Thus, the overall structural order relies on two parameters: the novel concept of degree of paracrystallinity ( i.e. , paracrystalline volume/mass fraction, introduced here for the first time) and the lattice distortion parameter of paracrystalline domains ( g -parameter from X-ray scattering). Structural parameters of the model are correlated with long-range charge carrier transport, revealing that charge transport in semi-paracrystalline materials is particularly sensitive to the interconnection of paracrystalline domains. 

Discrepancies in reported values of exciton binding energy (E_b) for organic semiconductors (OSs) necessitate a comprehensive study. Traditionally, E_bis defined as the difference between the transport gap (E_t) and the optical gap (E_opt). Here, the E_bvalues of PBnDT‐TAZ polymer variants are determined using two commonly employed methods: a combination of ultraviolet photoemission spectroscopy and low‐energy inverse photoemission spectroscopy (UPS‐LEIPS) and solid‐state cyclic voltammetry (CV). E_bvalues obtained by UPS‐LEIPS show low dispersion and no clear correlation with the polymer structure and thedielectric properties. In contrast, CV reveals a larger dispersion (200 meV‐1 eV) and an apparent qualitative E_b‐molecular structure correlation, as the lowest E_bvalues are observed for oligo‐ethylene glycol side chains. This discrepancy is discussed by examining the implications of the traditional definition of E_b. Additionally, the impact of both intrinsic and extrinsic factors contributing to the derived experimental values of E_tis discussed. The differences in intrinsic and extrinsic factors highlight the context‐dependent nature of measurement when drawing global conclusions. Notably, the observed E_btrend derived from CV is not intrinsic to the pure materials but likely linked to electrolyte swelling and associated changes in dielectric environment, suggesting that high‐efficiency single‐material organic photovoltaics with low E_bmay be possible via high dielectric materials.