Thesis--Ph. D., University of Hong Kong. / Typewritten.

Photoelectrochemical cells (PEC) and microbial fuel cells (MFC) are two promising environmental technologies with the purposes of energy production and pollutant degradation. In this study, p-type Cu2O thin film electrodes were synthesized by electrodeposition on the ITO glass. The influences of various electrodeposition conditions, including the deposition potential, temperature, electrolyte pH, substrates and deposition duration on the morphology and the photoelectrochemical properties of the Cu2O films were investigated. The so-called p-type micro-crystal Cu2O thin film photocathodes were synthesized at -0.4 V, 70 °C and pH 10. An innovative composite Cu2O/TiO2 photoelectrode was developed by dip-coating TiO2 on the surface of the Cu2O film. The outer TiO2 layer would help reduce the electron-hole recombination and hence improve the catalyst stability. The photocatalyst was shown to be capable of photocatalytic degradation of model pollutants. Under simulated solar irradiation, methylene blue, acridine orange, and bromocresso brilliant blue G were effectively degraded in the Cu2O-based PEC. The composite Cu2O/TiO2 photoelectrode could further enhance the photodegradation of the dyes. For the study on MFC with the saline wastewater-inoculated MFCs, an electricity output of 581 mW/m2 could be achieved at a NaCl concentration of 200 mM. Based on the characterization of the bioande using the electrochemical impedance spectroscopy (EIS) technique, the R(QR)(QR) model, instead of the conventional R(QR) model, was found to fit well with the EIS data of the carbon cloth bioanode. The results support the two-interface-based physical model for the description of the bioanode, including an interface on the flat electrode and the other for the porous biofilm matrix. The new model was employed to monitor the biofilm formation and development on the carbon clothe anode during the MFC start-up. In addition, photocatalytic MFC was developed by using the Cu2O film as the photocathode for the MFC. With the simulated solar light illumination, the PMFC open circuit voltage could be increased by 200 mV comparing to the MFC test. Moreover, the cathode material (Cu2O) is much less expensive than Pt used by common MFCs. / published_or_final_version / Civil Engineering / Master / Master of Philosophy

With the growing needs for energy, photovoltaic solar cells have attracted increasing research interests owing to its potentially renewable, feasible and efficient applications. Compared to its inorganic counterparts, organic solar cell (OSC) is highly desirable due to the low-cost processing, light weight, and the capability of flexible applications. While rapid progress has been made with the conversion efficiency approaching 10%, challenges towards high performance OSCs remain, including further improving device efficiency, fully realizing flexible applications, achieving more feasible large-area solution process and extending the stability of organic device. Having understood the key technical issues of designing high performance OSCs, we focus our work on (1) introducing flexible graphene transparent electrodes into OSCs as effective anode and cathode; (2) interface engineering of metal oxide carrier transport layers (CTLs) in OSCs through incorporating plasmonic metal nanomaterials ;(3)proposing novel film formation approach for solution-processed CTLs in OSCs in order to improve the film quality and thus device performance. The detailed work is listed below: 1. Design of transparent graphene electrodes for flexible OSCs Flexible graphene films are introduced into OSCs as transparent electrodes, which complement the flexibility of organic materials. We demonstrate graphene can function effectively as both the anode and cathode in OSCs: a) Graphene anode: we propose an interface modification for graphene to function as anode as an alternative to using aconventional polymer CTL. Using the proposed interfacial modification, graphene OSCs show enhanced performance. Further analysis shows that our approach provides favorable energy alignment and improved interfacial contact. b) Graphene cathode: efficient OSCs using graphene cathode are demonstrated, using a new composite CTL of aluminum-titanium oxide (Al-TiO2).We show that the role of Al is two-fold: improving the wettability as well as reducing the work function of graphene. To facilitate electron extraction, self-assembledTiO2is employed on the Al-covered graphene, which exhibits uniform morphology. 2. Incorporation of plasmonic nanomaterialsinto the metal oxide CTLinOSCs By incorporating metallic nanoparticles (NPs) into the TiO2CTLin OSCs, we demonstrate the interesting plasmonic-electrical effect which leads to optically induced charge extraction enhancement. While OSCs using TiO2CTL can only operate by ultraviolet (UV)activation, NP-incorporated TiO2enables OSCs to perform efficiently at a plasmonic wavelength far longer than the UV light. In addition, the effciency of OSCs incorporated with NPs is notably enhanced. We attribute the improvement to the charge injection of plasmonically excited electrons from NPs into TiO2. 3. Formation of uniform TiO2CTLfor large area applications using a self-assembly approach A solution-processed self-assembly method is proposed for forming large-area high-quality CTL films. Owing to the careful control of solvent evaporation, uniform film is formed, leading to enhanced OSC performance. Meanwhile, our method is capable of forming large-area films. This approach can contribute to future low-cost, large-area applications. / published_or_final_version / Electrical and Electronic Engineering / Doctoral / Doctor of Philosophy

published_or_final_version / Chemistry / Master / Master of Philosophy

No description available.

No description available.

The direct methanol fuel cell (DMFC) is considered to be a promising power source for portable electronic applications and transportation. At present there are several challenges that need to be addressed before the widespread commercialization of the DMFC technology can be implemented. The methanol electro oxidation reaction is sluggish, mainly due to the strong adsorption of the reaction intermediate carbon monoxide on platinum. Further, methanol crosses over to the cathode, which decreases the fuel utilization and causes cathode catalyst poisoning. Another issue is the accumulation of the reaction product CO₂ (g) in the anode, which increases the Ohmic resistance and blocks reactant mass transfer pathways. A novel anode configuration is proposed to address the aforementioned challenges. An extended reaction zone (thickness = ∼100-300 µm) is designed to facilitate the oxidation of methanol on sites that are not close to the membrane-electrode interface. Thus, the fuel concentration near the membrane may decrease significantly, which may mitigate adverse effects caused by methanol cross-over. The structure of the fibrous electrode, with its high void space, is believed to aid the disengagement of CO₂ gas. In this thesis the first objective was to deposit dispersed nanoparticle PtRu(Mo) catalysts onto graphite felt substrates by surfactant mediated electrodeposition. Experiments, in which the surfactant concentration, current density, time and temperature were varied, were conducted with the objective of increasing the active surface area and thus improving the reactivity of the electrodes with respect to methanol electro-oxidation. The three-dimensional electrodes were characterized with respect to their deposit morphology, surface area, composition and catalytic activity. The second objective of this work was to utilize the catalyzed electrodes as anodes for direct methanol fuel cell operation. The fuel cell performance was studied as a function of methanol concentration, flow rate and temperature by using a single cell with a geometric area of 5 cm². Increased power densities were obtained with an in-house prepared 3D PtRu anode compared to a conventional PtRu catalyst coated membrane. Coating graphite felt substrates with catalytically active nanoparticles and the utilization of these materials, is a new approach to improve the performance of direct fuel cells.

L – Ascorbic acid is a compound of great importance as it is vital to immune response and wound healing but it cannot be synthesised by some mammals, including humans. L- Ascorbic acid was also found to play an important role in the body as a free – radical scavenger, which may help to prevent free – radical induced diseases such as cancer and Parkinson’s disease. In foods, it is found in many fruits, especially in citrus fruits and berries, in vegetables and in beverages, especially those derived from fruit juices. Despite its wide presence in vegetables, many people do not acquire much Vitamin C this way. So very important is vitamin C. PI–50-1 model potentiostat, connected to Epsilon EC-2000-XP ( Ver.1,50,69_XP) programmer, and computer. The experiments were performed in a three-electrode cell, containing glassy carbon working electrode and counter-electrode (A = 0,07 cm2). Saturated Ag/AgCl reference electrode. All potential values reported refer to this reference electrode. The electrochemical oxidation of ascorbic acid at poly(N-methylaniline) modified electrode has been studied. The proposed mechanism explains the ability of poly(N-methylaniline) to electro-catalyze the anodic oxidation of ascorbic acid. It has been shown that poly(N-methylaniline) modified electrodes can be used for ascorbic acid assay within a pH range of 4,41 – 6,70, operating potential window of 0,25 – 0,4 V vs. Ag/AgCl, showing a linear range of response up to 1 mM, and a lower detection... [to full text]

<p>In this work a modified polyol method was developed to synthesize in-house catalysts. The method was modified for maximum delivery of product and proved to be quick and efficient as well as cost effective. The series of IH catalysts were characterized using techniques such as UV-vis and FT-IR spectroscopy, TEM, XRD, ICP and CV.</p>

The dielectric properties of polymeric thin films (100-200 nm) are hard to measure with the standard approaches as the samples aren't free standing necessitating a supporting substrate. Consequently, a planar interdigitated sample holder has been designed to hold the thin film where the polymeric capacitance was derived from the passing fringing fields. The electrodes were fabricated by creating 120 nm trenches in a SiO2/Si wafer; 20 nm Cr was deposited as an adhesion layer prior to the deposition of Cu by thermal evaporation. The electrical measurements were implemented using HP 4294A and a probe station. Devices of 20 to 70 fingers were measured and the results were compared to the analytical and finite element simulation. At 10 KHz, the total measured capacitance of a 20-finger device was about 8 pF with 3 % represented the polymeric contribution. The measurements differed from the calculations or finite modeling results by about 12%.