The rise of organometal halide perovskite materials with extremely intriguing properties have opened a new horizon in the design of high speed and low price optoelectronic devices. The bandgap in the crystalline structure of these materials can be easily tuned for various applications and their dominant non-excitonic dynamics eliminate the requirement of a bulk or heterostructure for charge carrier separation. These unique properties increase the photo-sensitivity of perovskite-based optoelectronics and provide them with a low time constant, resulting in high precision fast devices. Realization of perovskite-based devices translates directly to inexpensive and simplified architectures of optoelectronic systems. In perovskite-based devices, costly silicon or wide bandgap semiconductor fabrication technology is largely replaced by solution processable methods. Their bandgap tunability allows the reduction of the required optical accessories and interconnects in optoelectronic components. For instance, a tuned perovskite-based detector can substitute a narrowband detecting system consisting of a conventional detector and its required optical accessories such as lenses and color filters. These properties of perovskite-based devices lead to the realization of inexpensive, low power and high-performance optoelectronic systems. In this work, the design of a narrowband, low noise, high performance and stable photodetector based on organic-inorganic hybrid perovskite structure is proposed. The full width at half maximum (FWHM) of the device would be in the nanometer range. The response of the device can be tuned using either different ratios of the lead salts or synthetic dyes (macromolecules) in the crystalline structure for color discrimination in machine vision and imaging applications. Non-excitonic photocarrier generation, tunability of the optical bandgap and low voltage requirements for charge carrier generation are the keys to the utility of this optoelectronic device. The goals of this project were to identify the required functional materials (lead salts and synthetic dyes based on their molecular structures) and optimize their performance; the study of their effect on the charge collection narrowing mechanism and bandwidth specifications defined for detectivity, linear dynamic range (LDR) and photoresponse speed. To achieve these goals, it was proposed to study the light detection properties as well as spectroscopic and semiconductor parameter characteristics of fabricated devices. The design considerations of such devices are versatile and may be modulated for different applications.

Magister Scientiae - MSc (Chemistry) / Pollutants such as polycyclic aromatic hydrocarbons (PAHs) are known for their toxic effects which may lead to the cause of degenerative diseases in both humans and animals. PAHs are widespread in the environment, and may be found in water, food, automotive industry and petrochemical industries to name but a few sources. Literature reports have highlighted industrial workplace exposure to PAHs as a leading cause for development of cancer in workers. Particularly, workers in the petrochemical industry are adversely affected and the incidence of skin and lung cancer in this population group is high. The United States of America in its guidelines developed by environmental protection agency (EPA) has identified 18 PAHs as priority pollutants. Among these are anthracene, benzo[a]pyrene and pyrene which have been selected as the focal point of this study due to their significance in the petrochemical industry. Due to the carcinogenic and mutagenic properties reported in literature for certain PAHs, there have been monitoring procedures taken in most countries around the world. The commonly used analytical methods for the detection of PAHs from industrial samples are high performance liquid chromatography (HPLC) coupled to fluorescence detection, membrane filtration, ozonation and reverse osmosis. Analysis of PAHs from the petrochemical industry is typically performed by HPLC method as well as sono-degredation in the presence of oxygen and hydrogen peroxide.

Solution-processed lead sulfide quantum dots (PbS QDs) are an excellent candidate for photodetector applications because they exhibit broadband absorption, a wide range of tuneable bandgaps, high stability in air, and mechanical flexibility. However, a crucial criterion for the fabrication of high-performance photodetectors is the selection of the ligands, which can facilitate charge carrier transport between the PbS QDs and passivate the surface defects. In this work, the authors have studied the effect of traps on the performance of PbS QD photodetectors that are fabricated using different types of ligands, using intensity-dependent photoresponse dynamics. The best devices with lead halide ligands show a dark current density of 5 × 10−9 A cm−2 at −0.2 V, which is one of the lowest values reported thus far for solution-processed PbS QD-based photodetectors. Moreover, these devices show a high linear dynamic range (≈90 dB) and high detectivity (>1013 Jones), in addition to an f-3 dB of greater than 100 kHz without the application of an external voltage bias at a wavelength of 784 nm. These results suggest that with an appropriate selection of ligands, solution-processed photodetectors with a lower density of traps and a better device performance can be fabricated.