arXiv subjects

Anton Kirch

Publications and source records attributed to Anton Kirch.

8 recordsLinked to original sources

arXiv2026

Modifying Electrochemical Doping in Light-Emitting Electrochemical Cells with Gold Nanoparticles

Electrochemical doping offers dynamic control of the electronic properties of organic semiconductors, and it is the enabling feature of a range of technologies, including electrochemical transistors, energy-storage devices, light-emitting electrochemical cells (LECs), and bioelectronics. Electrochemical doping is commonly controlled by the selection of the constituents in the active material of the device or the applied voltage bias, but herein we report that the incorporation of Au nanoparticles (Au-NPs) at an electrode interface can constitute an alternative control parameter. The LEC features balanced p- and n-type electrochemical doping that forms a p-n junction doping structure in its active material, and we find that it is possible to reshape this doping profile by incorporating Au-NPs at an electrode interface. Specifically, we establish that the inclusion of neat non-capped Au-NPs at the anodic interface shifts the p-n junction (i.e., the emission zone) away from the anode. In contrast, the inclusion of Au-NPs capped with sodium citrate is found to reverse this behavior, so that the emission zone is instead moved towards the anode. We utilize this control parameter to shift the emission zone towards a position of constructive (destructive) interference, as manifested in a strong increase (decrease) of the LEC emission efficiency. Our findings establish an interfacial strategy for modulating the spatial profile of electrochemical doping and tuning device performance without altering the chemistry of the active material, relying instead on the surface modification of one electrode. This approach is important because it provides a versatile and minimally invasive route to optimize electrochemical devices while preserving the intrinsic properties and formulation of the active material.

cond-mat.mtrl-sci↗

arXiv2026

Round-Robin Test of a Light-Emitting Electrochemical Cell: Establishing a Reference Protocol for Quality Research

Emerging technologies benefit from a jointly established reference protocol, which can lower the bar of entry for new researchers while serving as a calibration standard for established actors. The light-emitting electrochemical cell (LEC) combines electrochemistry and optoelectronics in an intricate manner, and it can by that enable sustainable and commercially relevant printing fabrication of emissive thin-film devices. However, LEC performance is sensitive to a range of material and processing parameters, which frequently results in inadequate, or even erroneous, device evaluation. With this in mind, we present herein a LEC reference protocol, which details the sourcing of materials and the procedures and parameters for robust device fabrication and operation. The protocol has been tested across nine international research groups, and the collected results from this interlaboratory round-robin test confirm that good LEC performance can be reproducibly obtained following our protocol. We also identify common pitfalls that can arise during LEC development, and present practical steps for attaining optimum LEC performance. We hope this reference protocol will improve the quality of future LEC research and serve as a guide for future researchers entering this vibrant field.

cond-mat.soft↗

arXiv2025

In-operando dipole orientation for bipolar injection from air-stable electrodes into organic semiconductors

Efficient charge-carrier injection from air-stable electrodes into organic semiconductors (OSCs) is essential for fabricating solution-processed organic optoelectronic devices under ambient conditions. Today, this is typically achieved by incorporating doped OSC interlayers, introducing self-assembled dipole monolayers, or adding mobile ions to the active material (AM). Here, we demonstrate an alternative approach that eliminates the need for additional injection layers or ionic additives. We achieve this by blending the dipolar compound TMPE-OH into the electroluminescent polymer Super Yellow (SY) and depositing this sole AM between two air-stable electrodes, forming a single-layer, dipole-doped OLED (D-OLED). By tracking its transient voltage-luminance response, performing impedance spectroscopy, and comparing these characteristics with two other single-layer device concepts, i.e. a neat-SY OLED without a dipolar compound and a light-emitting electrochemical cell (LEC) containing mobile ions, we can establish that the auxiliary dipoles in the D-OLED reorient under the applied driving voltage, enabling immediate luminance turn-on and lowering the injection barriers at both electrodes. Finally, we demonstrate that the D-OLED achieves current efficacies comparable to those of SY OLEDs incorporating dedicated injection layers or LECs. Our study establishes dipolar doping as a practical strategy for efficient bipolar charge injection from air-stable electrodes in solution-processed organic semiconductor devices.

cond-mat.mtrl-sci↗

arXiv2024

Impact of the electrode material on the performance of light-emitting electrochemical cells

Light-emitting electrochemical cells (LECs) are promising candidates for fully solution-processed lighting applications because they can comprise a single active-material layer and air-stable electrodes. While their performance is often claimed to be independent of the electrode material selection due to the in-situ formation of electric double layers (EDLs), we demonstrate conceptually and experimentally that this understanding needs to be modified. Specifically, the exciton generation zone is observed to be affected by the electrode work function. We rationalize this finding by proposing that the ion concentration in the injection-facilitating EDLs depends on the offset between the electrode work function and the respective semiconductor orbital, which in turn influences the number of ions available for electrochemical doping and hence shifts the exciton generation zone. Further, we investigate the effects of the electrode selection on exciton losses to surface plasmon polaritons and discuss the impact of cavity effects on the exciton density. We conclude by showing that the measured electrode-dependent LEC luminance transients can be replicated by an optical model that considers these electrode-dependent effects to calculate the attained light outcoupling of the LEC stack. As such, our findings provide rational design criteria considering the electrode materials, the active-material thickness, and its composition in concert to achieve optimum LEC performance.

physics.optics↗

arXiv2024

Interdot Lead Halide Excess Management in PbS Quantum Dot Solar Cells

Light-harvesting devices made from PbS quantum dot (QD) absorbers are one of the many promising technologies of third-generation photovoltaics. Their simple, solution-based fabrication together with a highly tunable and broad light absorption makes their application in newly developed solar cells particularly promising. In order to yield devices with reduced voltage and current losses, PbS QDs need to have strategically passivated surfaces, most commonly achieved through lead iodide and bromide passivation. The interdot spacing is then predominantly filled with residual amorphous lead halide species that remain from the ligand exchange, thus hindering efficient charge transport and reducing device stability. Herein, we demonstrate that a post-treatment by iodide based 2-phenylethlyammonium salts (X-PEAI) and intermediate 2D perovskite formation can be used to manage the lead halide excess in the PbS QD active layer. This treatment results in improved device performance and increased shelf-life stability, demonstrating the importance of interdot spacing management in PbS quantum dot photovoltaics.

physics.app-ph↗

arXiv2022

Accurate wavelength tracking by exciton spin mixing

Wavelength discriminating systems typically consist of heavy benchtop-based instruments, comprising diffractive optics, moving parts, and adjacent detectors. For simple wavelengths measurements, such as lab-on-chip light source calibration or laser wavelength tracking, which do not require polychromatic analysis and cannot handle bulky spectroscopy instruments, light-weight, easy-to-process, and flexible single-pixel devices are attracting increasing attention. Here, we propose a device for wavelength tracking with room-temperature phosphorescence at the heart of its functionality that demonstrates a resolution down to one nanometer and below. It is solution-processed from a single host-guest system comprising organic room-temperature phosphors and colloidal quantum dots. The share of excited triplet states within the photoluminescent layer is dependent on the excitation wavelength and determines the afterglow intensity of the film, which is tracked by a simple photodetector. Finally, an all-organic thin-film wavelength sensor and two applications are demonstrated where our novel measurement concept successfully replaces a full spectrometer.

physics.optics↗

arXiv2022

A simple strategy to measure the contact resistance between metals and doped organic films

Charge injection from electrodes into doped organic films is a widespread technology used in the majority of state-of-the-art organic semiconductor devices. Although such interfaces are commonly considered to form Ohmic contacts via strong band bending, an experiment that directly measures the contact resistance has not yet been demonstrated. In this study, we use a simple metal/doped organic semiconductor/metal stack and study its voltage-dependent resistance. A transport layer thickness variation proves that the presented experiment gains direct access to the contact resistance of the device. We can quantify that for an operating current density of 10mA/cm2 the investigated material system exhibits a voltage drop over the metal/organic interface of about 200mV, which can be reduced by more than one order of magnitude when employing an additional injection layer. The presented experiment proposes a simple strategy to measure the contact resistance between any metal and doped organic film without applying numerical tools or elaborate techniques. Furthermore, the simplistic device architecture allows for very high, homogeneous, and tunable electric fields within the organic layer, which enables a clear investigation of the Poole-Frenkel effect.

physics.app-ph↗

arXiv2015

A Silicon-Singlet Fission Parallel Tandem Solar Cell Exceeding 100 % External Quantum Efficiency

Silicon solar cells dominate the solar cell market with record lab efficiencies reaching almost 26%. However, after 60 years of research, this efficiency saturated close to the theoretical limit for silicon, and radically new approaches are needed to further improve the efficiency. Here we present parallel-connected tandem solar cells based on down-conversion via singlet fission. This design allows raising the theoretical power conversion efficiency limit to 45% with far superior stability under changing sunlight conditions in comparison to traditional series tandems. We experimentally demonstrate a silicon/pentacene parallel tandem solar cell that exceeds 100% external quantum efficiency at the main absorption peak of pentacene, showing efficient photocurrent addition and proving this design as a realistic prospect for real-world applications.

cond-mat.other↗