Abstract:Organic semiconductors require an energetic offset in order to photogenerate free charge carriers efficiently, owing to their inability to effectively screen charges. This is vitally important in order to achieve high power conversion efficiencies in organic solar cells. Early heterojunction‐based solar cells were limited to relatively modest efficiencies (<4%) owing to limitations such as poor exciton dissociation, limited photon harvesting, and high recombination losses. The development of the bulk heterojun… Show more
“…[ 41 ] Thus, a bulk heterojunction with the appropriate energy level matching significantly overcame the exciton recombination and improved device performance. [ 42 ] 2D MOF films are a relatively emergent porous material and may become a promising candidate for application in new types of BHJ photoelectric devices, such as photodetectors, solar cells, artificial optoelectronic synapses, or simulated retinas.…”
The preparation of large‐area 2D conductive metal–organic framework (MOF) films remains highly desirable but challenging. Here, inspired by the capillary phenomenon, a face‐to‐face confinement growth method to grow conductive 2D Cu2(TCPP) (TCPP = meso‐tetra(4‐carboxyphenyl)porphine) MOF films on dielectric substrates is developed. Trace amounts of solutions containing low‐concentration Cu2+ and TCPP are pumped cyclically into a micropore interface to produce this growth. The crystal structures are confirmed with various characterization techniques, which include high‐resolution atomic force microscopy and cryogenic transmission electron microscopy (Cryo‐TEM). The Cu2(TCPP) MOF film exhibit an electrical conductivity of ≈0.007 S cm−1, which is approximately four orders of magnitude higher than other carboxylic‐acid‐based MOF materials (10−6 S cm−1). Other wafer‐scale conductive MOF films such as M3(HHTP)2 (M = Cu, Co, and Ni; HHTP = 2,3,6,7,10,11‐triphenylenehexol) can be produced utilizing this strategy and suggests this method has widescale applicability potential.
“…[ 41 ] Thus, a bulk heterojunction with the appropriate energy level matching significantly overcame the exciton recombination and improved device performance. [ 42 ] 2D MOF films are a relatively emergent porous material and may become a promising candidate for application in new types of BHJ photoelectric devices, such as photodetectors, solar cells, artificial optoelectronic synapses, or simulated retinas.…”
The preparation of large‐area 2D conductive metal–organic framework (MOF) films remains highly desirable but challenging. Here, inspired by the capillary phenomenon, a face‐to‐face confinement growth method to grow conductive 2D Cu2(TCPP) (TCPP = meso‐tetra(4‐carboxyphenyl)porphine) MOF films on dielectric substrates is developed. Trace amounts of solutions containing low‐concentration Cu2+ and TCPP are pumped cyclically into a micropore interface to produce this growth. The crystal structures are confirmed with various characterization techniques, which include high‐resolution atomic force microscopy and cryogenic transmission electron microscopy (Cryo‐TEM). The Cu2(TCPP) MOF film exhibit an electrical conductivity of ≈0.007 S cm−1, which is approximately four orders of magnitude higher than other carboxylic‐acid‐based MOF materials (10−6 S cm−1). Other wafer‐scale conductive MOF films such as M3(HHTP)2 (M = Cu, Co, and Ni; HHTP = 2,3,6,7,10,11‐triphenylenehexol) can be produced utilizing this strategy and suggests this method has widescale applicability potential.
“…Despite the advantages, mixing two or more components presents challenges to achieve an optimum morphology. [ 17 ] In fact, this usually involves a trial‐and‐error approach and finding a relationship between solar cell efficiency, microstructure, and thin‐film formation kinetics has been challenging. The Flory–Huggins interaction parameter has been reported as a powerful method to correlate the device performance with phase purity and amorphous–amorphous phase diagrams.…”
Section: Stability Of Opvmentioning
confidence: 99%
“…Such properties led to expectations that bulk heterojunction (BHJ) OPVs might be able to compete with their silicon‐based counterparts at some point. [ 17 ] However, significant emphasis has been placed on the production of high‐grade c‐Si in recent years, drastically driving down its cost, as dictated by Swanson's law. [ 18 ] As such, emerging photovoltaic technologies, including OPV, have struggled to compete with silicon on the basis of levelized cost of electricity, with recent costs of c‐Si photovoltaics estimated at 0.30 $ W p −1 .…”
Recent advances in the development of organic photovoltaic (OPV) materials has led to significant improvements in device performance; now closing in on the 20% efficiency threshold. Despite these improvements in performance, the commercial viability of organic photovoltaic products remains elusive. In this perspective, the current limitations of high performing blends are uncovered, particularly focusing on the industrial upscaling considerations of these materials, such as synthetic scalability, active layer processing, and device stability. Moreover, a simplified metric, namely, the scalability factor (SF), is introduced to evaluate the scale‐up potential of specific OPV materials and blends thereof. Of the most popular molecular design strategies investigated in recent times, it is found that the use of Y‐series nonfullerene acceptors (NFAs) and synthetically simple materials, such as PTQ‐10 and ternary blends, are most effective at maximizing the efficiency without negatively impacting the SF. Furthermore, the improvements that are needed, in terms of device processability and stability, are considered for industrial scale‐up and final product application. Finally, an outlook of organic photovoltaics is provided both from a perspective of important research avenues and applications that can be exploited.
“…The exploration of novel organic semiconductive materials for the development of bulk heterojunction (BHJ) solar cells has led to considerable progress in device performance in the past years. [1][2][3] The careful design of chemical structures, which takes advantage of the input provided by the continuous effort of synthetic chemists, together with a better understanding of the relationship between structure, properties, and performance are driving the development of increasingly high-performing organic photovoltaic materials. [4][5][6][7] Indeed, power conversion efficiencies (PCEs) of organic solar cells are now above 18%, confirming the role of BHJs as a promising technology for future clean energy supply.…”
Here is reported the synthesis of a family of thiophene-based heptamers alternating electron donor (D) and acceptor (A) units in a D–A′–D–A–D–A′–D sequence. Their multiple roles as active materials in BHJ solar cells are presented.
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