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Built-in voltage enhanced by in-situ electrochemical polymerized undoped conjugated hole-transporting modifier in organic solar cells
摘要： Herein, a new electropolymerized (EP) film named poly-triphenylcarbazole fluoranthene (p-TPCF) has been in-situ synthesized by electrochemical cyclic voltammetry method, and applied to tune the work-function (WF) of the PEDOT:PSS hole-transporting layer (HTL) in organic solar cells (OSCs). Multi techniques, including Kelvin probe force microscopy (KPFM), light intensity dependent solar cell characterization, Mott-Schottky analysis, transient photovoltage (TPV) and transient photocurrent (TPC) measurements, have been explored to provide insights into the mechanism. Benefiting from deeper work-function (WF), larger built-in voltage (Vbi), decreased recombination, longer carrier lifetime, the devices with EP film exhibited superior device performance with simultaneously enhanced Voc, Jsc and FF.
关键词： PEDOT:PSS,built-in voltage,work-function tuning,organic solar cells,carrier lifetime,electropolymerized film,charge recombination
更新于2025-09-19 17:13:59
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The green poly-lysine enantiomers as electron-extraction layers for high performance organic photovoltaics
摘要： In this study, we first revealed green materials – poly-lysines (poly-L-lysine and poly-L-lysine blend poly-D-lysine) – as electron-extraction layers (EELs) in organic photovoltaics (OPVs). The distinct configurations of poly-lysine enantiomers were verified by conducting zeta potential analysis, and their work function (WF)-tuning capabilities for indium tin oxide (ITO) were affirmed by ultraviolet photoelectron spectroscopy (UPS). These two poly-lysine groups, with different arrangements of the amino groups that built up different surface dipoles on the ITO substrate, altered the surface energy and WF of ITO. Poly-L-lysine optimized the WF of ITO for efficient carrier transport in the OPV device, in the electron transporting layer-free OPV devices, and we observed a high power conversion efficiency (PCE) of 10.01% in the device configuration of ITO/interlayer/BHJ/MoO3/Ag. As the first examination of poly-lysine enantiomers for OPVs, we provided the WF-tuning functions – increasing polarity as an interfacial dipole is formed at the corresponding interface, and discovered a promising interfacial material possessing high efficiency and benefitting from a long-term stability to perform in a stable PCE with about 80% of its original PCE remaining after continuous heat and light treatment for 400 hours.
关键词： interfacial dipole,organic photovoltaics,electron-extraction layers,poly-lysine,work function tuning
更新于2025-09-16 10:30:52
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Self-Assembled Monolayers with Distributed Dipole Moments Originating from Bipyrimidine Units
摘要： The concept of distributed dipoles in monomolecular self-assembly on solid substrates was tested for the example of thiolate self-assembled monolayers (SAMs) on Au(111) containing dipolar 2,5?-bipyrimidine units. These were attached to a thiol anchoring group either directly or via a phenylene-methylene spacer, with the spacer decoupling the dipolar moiety from the substrate and promoting layer formation. As expected, the SAMs containing spacer groups exhibited a higher quality, including a higher packing density and nearly upright molecular orientation. The electrostatic effects of the dipolar bipyrimidine moieties were tested through C 1s and N 1s photoemission spectra, where electrostatic core-level shifts impact the shapes of the spectra. Additionally, changing the orientation of the dipoles allows a variation of the work function over a range of ~1.35 eV. The experiments were complemented by density-functional theory calculations. The work function tuning range was reasonably high, but smaller than expected considering that for SAMs with a single embedded pyrimidine group per molecule work-function changes already amounted to ~1.0 eV. This behavior is rooted in an asymmetry of the studied SAMs: For dipoles pointing away from the substrate, the expected doubling of the work function change between monopyrimidine and bipyrimidine SAMs essentially occurs. Conversely, for the downward-oriented pyrimidine dipoles, the second polar ring has hardly any effect. Consistent observations were made for the core-level shifts. We discuss several factors, which are potentially responsible for this asymmetry, like disorder, depolarization, or Fermi-level pinning. Of these, the most likely explanation is the adsorption of airborne contaminants interacting with the nitrogen atoms in the immediate vicinity of the outer surface, which are present only in films with downward oriented dipoles. In spite of these complications, some of the introduced distributed dipole SAMs serve as important model systems for understanding electrostatic effects at interfaces. They are also of interest for controlling carrier-injection barriers in organic (opto)electronic devices.
关键词： Bipyrimidine Units,Distributed Dipole Moments,Self-Assembled Monolayers,Organic (Opto)electronic Devices,Work Function Tuning
更新于2025-09-12 10:27:22