Date of Award

Spring 5-10-2019

Document Type

Thesis

Degree Name

Master of Science (MS)

Department

Chemistry

First Advisor

Dr. Ram Gupta

Keywords

Perovskite, Water splitting, Supercapacitor, OER, HER, pseudocapacitance

Abstract

Recent changes in global weather patterns have accented the need a shift from fossil fuels to a cleaner energy option. As part of an overall plan, hydrogen production for fuel cells offer substantial power without carbon emissions. Overall water splitting, with the aid of a low cost electrocatalyst could prove to be an abundant green fuel source. Utilizing readily available transition metals, three perovskite nanostructures were studied as a multifunctional material for hydrogen production as well as an energy storage material. LaCoO3 (LCO), LaFeO3 (LFO), and LaMnO3 (LMO) were synthesized and characterized by X-ray diffraction (XRD) and then dip coated onto nickel foam as electrodes in a standard three electrode system. The electrochemical properties were analyzed with electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and cyclic voltammetry (CV) for its electro-catalytic activity towards both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) as well as its effectiveness as a supercapacitor. It was shown that electrocatalytic activity toward OER was highly dependent on the material composition. Accordingly, LFOhad the lowest overpotential voltage of 316 mV at 10 mA/cm2 compared with 376 mV (LCO) and 419 mV (LMO). Toward HER, LMOshowed overpotential voltage of 176 mV at 10 mA/cm2, while LCO and LFO showed 221 mV and 230 mV, respectively. Measured over a range of current densities, the specific capacitance of LCO remained higher (~100) F/g over LCO (~45 F/g) and LFO (~35 F/g). An altered synthetic method was employed to investigate the affects of structure directing (chelating) agents on electro-catalytic activity. Replacement of glycine with citric acid in the synthesis process was found to improve the structure characteristics and electrochemical properties of LFO. Structural improvements for LCO and LMO were unfavorable with alteration as shown by XRD. Further investigation and understanding of structure directing agents and oxygen vacancy manipulation is needed for greater material efficiency.

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