Photodiodes based in La0.7Sr0.3MnO3/single layer MoS2 hybrid vertical heterostructures

The fabrication of artificial materials by stacking of individual two-dimensional (2D) materials is amongst one of the most promising research avenues in the field of 2D materials. Moreover, this strategy to fabricate new man-made materials can be further extended by fabricating hybrid stacks between 2D materials and other functional materials with different dimensionality making the potential number of combinations almost infinite. Among all these possible combinations, mixing 2D materials with transition metal oxides can result especially useful because of the large amount of interesting physical phenomena displayed separately by these two material families. We present a hybrid device based on the stacking of a single layer MoS2 onto a lanthanum strontium manganite (La0.7Sr0.3MnO3) thin film, creating an atomically thin device. It shows a rectifying electrical transport with a ratio of 103, and a photovoltaic effect with Voc up to 0.4 V. The photodiode behaviour arises as a consequence of the different doping character of these two materials. This result paves the way towards combining the efforts of these two large materials science communities.Comment: 1 table, 4 figures (+9 supp. info. figures

An all-glass microfluidic network with integrated amorphous silicon photosensors for on-chip monitoring of enzymatic biochemical assay

A lab-on-chip system, integrating an all-glass microfluidics and on-chip optical detection, was developed and tested. The microfluidic network is etched in a glass substrate, which is then sealed with a glass cover by direct bonding. Thin film amorphous silicon photosensors have been fabricated on the sealed microfluidic substrate preventing the contamination of the micro-channels. The microfluidic network is then made accessible by opening inlets and outlets just prior to the use, ensuring the sterility of the device. The entire fabrication process relies on conventional photolithographic microfabrication techniques and is suitable for low-cost mass production of the device. The lab-on-chip system has been tested by implementing a chemiluminescent biochemical reaction. The inner channel walls of the microfluidic network are chemically functionalized with a layer of polymer brushes and horseradish peroxidase is immobilized into the coated channel. The results demonstrate the successful on-chip detection of hydrogen peroxide down to 18 mu M by using luminol and 4-iodophenol as enhancer agent

Photo-FETs: phototransistors enabled by 2D and 0D nanomaterials

The large diversity of applications in our daily lives that rely on photodetection technology requires photodetectors with distinct properties. The choice of an adequate photodetecting system depends on its application, where aspects such as spectral selectivity, speed, and sensitivity play a critical role. High-sensitivity photodetection covering a large spectral range from the UV to IR is dominated by photodiodes. To overcome existing limitations in sensitivity and cost of state-of-the-art systems, new device architectures and material systems are needed with low-cost fabrication and high performance. Low-dimensional nanomaterials (0D, 1D, 2D) are promising candidates with many unique electrical and optical properties and additional functionalities such as flexibility and transparency. In this Perspective, the physical mechanism of photo-FETs (field-effect transistors) is described and recent advances in the field of low-dimensional photo-FETs and hybrids thereof are discussed. Several requirements for the channel material are addressed in view of the photon absorption and carrier transport process, and a fundamental trade-off between them is pointed out for single-material-based devices. We further clarify how hybrid devices, consisting of an ultrathin channel sensitized with strongly absorbing semiconductors, can circumvent these limitations and lead to a new generation of highly sensitive photodetectors. Recent advances in the development of sensitized low-dimensional photo-FETs are discussed, and several promising future directions for their application in high-sensitivity photodetection are proposed.Peer ReviewedPostprint (author's final draft

Machine Learning Optimization of p-Type Transparent Conducting Films

p-Type transparent conducting materials (p-TCMs) are important components of optoelectronic devices including solar cells, photodetectors, displays, and flexible sensors. Cu-Zn-S thin films prepared by chemical bath deposition (CBD) can have both high transparency in the visible range (>80%) as well as excellent hole conductivity (>1000 S cm-1). However, the interplay between the deposition parameters in the CBD process (metal and sulfur precursor concentrations, temperature, pH, complexing agents, etc.) creates a multidimensional parameter space such that optimization for a specific application is challenging and time-consuming. Here we show that strategic design of experiment combined with machine learning (ML) allows for the efficient optimization of p-TCM performance. The approach is guided by a figure of merit (FOM) calculated from the film conductivity and optical transmission in the desired spectral range. A specific example is shown using two steps of optimization using a selected subset of four experimental CBD factors. The ML model is based on support vector regression employing a radial basis function as the kernel function. 10-fold cross-validation was performed to mitigate overfitting. After the first round of optimization, predicted areas in the parameter space with maximal FOMs were selected for a second round of optimization. Films with optimal FOMs were incorporated into heterojunction solar cells and transparent photodiodes. The optimization approach shown here will be generally applicable to any materials synthesis process with multiple parameters

Organic Photodiodes with an Extended Responsivity using Ultrastrong Light-Matter Coupling

In organic photodiodes (OPDs) light is absorbed by excitons, which dissociate to generate photocurrent. Here, we demonstrate a novel type of OPD in which light is absorbed by polaritons, hybrid light-matter states. We demonstrate polariton OPDs operating in the ultra-strong coupling regime at visible and infrared wavelengths. These devices can be engineered to show narrow responsivity with a very weak angle-dependence. More importantly, they can be tuned to operate in a spectral range outside that of the bare exciton absorption. Remarkably, we show that the responsivity of a polariton OPD can be pushed to near infrared wavelengths, where few organic absorbers are available, with external quantum efficiencies exceeding those of a control OPD

Microfluidic cartridge with integrated array of amorphous silicon photosensors for chemiluminescence detection of viral DNA

Portable and simple analytical devices based on microfluidics with chemiluminescence detection are particularly attractive for point-of-care applications, offering high detectability and specificity in a simple and miniaturized analytical format. Particularly relevant for infectious disease diagnosis is the ability to sensitively and specifically detect target nucleic acid sequences in biological fluids. To reach the goal of real-life applications for such devices, however, several technological challenges related to full device integration are still to be solved, one key aspect regarding on-chip integration of the chemiluminescence signal detection device. Nowadays, the most promising approach is on-chip integration of thin-film photosensors. We recently proposed a portable cartridge with microwells aligned with an array of hydrogenated amorphous silicon (a-Si:H) photosensors, reaching attomole level limits of detection for different chemiluminescence model reactions. Herein, we explore its applicability and performance for multiplex and quantitative detection of viral DNA. In particular, the cartridge was modified to accommodate microfluidic channels and, upon immobilization of three oligonucleotide probes in different positions along each channel, each specific for a genotype of Parvovirus B19, viral nucleic acid sequences were captured and detected. With this system, taking advantage of oligoprobes specificity, chemiluminescence detectability, and photosensor sensitivity, accurate quantification of target analytes down to 70 pmol L-1 was obtained for each B19 DNA genotype, with high specificity and multiplexing ability. Results confirm the good detection capabilities and assay applicability of the proposed system, prompting the development of innovative portable analytical devices with enhanced sensitivity and multiplexed capabilities

Understanding and Engineering of Sub-gap States in Photodetection

Emerging applications for light sensing, including wearable electronics, internet of things and autonomous driving, are pushing conventional semiconductors technologies to their limits when it comes to ease of fabrication, power consumption and device design. Organic semiconductors are considered next-generation absorber materials for photodetection in the visible and near infrared part of the electromagnetic spectrum, which hold some promise of addressing the aforementioned problems of conventional materials. So far, only a handful of companies are putting organic semiconductors to the test for commercial photodetectors, however, research on organic photodetectors is thriving – in particular on photodetectors with a diode architecture called photodiodes. The goal is to make flexible, light-weight devices with improved performance metrics and high stability to realize viable alternatives to conventional photodiodes. The performance limits of organic photodiodes are often associated with the presence of electronic states with energies below the bandgap edge – the so-called sub-gap states. A powerful tool to study the properties of sub-gap states is to measure the external quantum efficiency (EQE), however, the subsequent analysis is complicated by the presence of static disorder and optical interference. In the first part of this work, it is shown how the true absorption coefficient can be extracted from a series of interference affected sub-gap EQE spectra of organic photodiodes with different thicknesses. In consequence, the effect of chemical structure modification on the absorption coefficient in the spectral range of charge transfer absorption is demonstrated. By adjusting the molecular energy levels through target chemical substitutions, a redshift and an increase of the oscillator strength are achieved. The increased spectral coverage in the near infrared is then exploited in micro-cavity photodiodes. The second part of this work deals with the sub-gap absorption coefficient of donor and acceptor materials and how it is affected by the molecular energy level offset. For materials with low energetic offset, it is shown that the sub-gap absorption coefficient follows the Urbach rule in the spectral range of excitonic absorption, dictating the broadening of the sub-gap absorption coefficient at energies right below the bandgap. Lastly, the origin of the high dark current in organic photodiodes is identified as non-radiative recombination via mid-gap trap states. An upper limit to the specific detectivity is calculated that is expected viable in organic photodiodes. The findings of this thesis contribute to the understanding of the sub-gap states by studying their absorption features and distinguishing them from the ubiquitous optical interference effects. The spectroscopic observation of mid-gap trap states is linked to the dark current generation dictating the upper performance limits of organic photodiodes