arXiv subjects

Jacob L. Poole

Publications and source records attributed to Jacob L. Poole.

3 recordsLinked to original sources

arXiv2020

In Situ characterization of the proton enhanced conductivity of 20nm TiO2 thin-films obtained on the surface of optical fiber

We report in situ characterized TiO2 thin-films deposited on optical fiber, having thicknesses in the 20-100nm range, and having enhanced conductivity values of 700S/cm upon interacting with hydrogen. This conductivity was achieved in pure hydrogen at 800-900C, having a measured activation energy of 0.26eV of the hopping type. Given the variability in the observed results, it is postulated that the highest conductivity achievable may be much greater than what is currently demonstrated. The conductivity is retained after cooling to ambient temperatures as confirmed by Hall measurements, and subsequent grazing-incidence x-ray diffraction and TEM measurements show the films to be in the rutile phase. The exceptional conductivity in these films is hypothesized to result from direct proton incorporation into the lattice populating the conduction band with excess electrons, or from altering the Titania lattice to form conductive Magneli phases. The films did not display any evidence of transformations, however formation of Magneli phases was confirmed for powders. These interesting results, observed by examining 20nm films on the surface of optical fiber in combination with the first impedance spectroscopy performed on films on optical fiber in high temperature Fuel Cell type environments, confirm hypotheses arrived at in prior publications where thin-films of Titania had optical properties which could only be explained by the current claim. Titania thin-films on optical-fiber are being explored for high temperature hydrogen derived energy generation, thermo-photonic energy conversion, and associated sensors due to their unique interactions with hydrogen.

cond-mat.mtrl-sci↗

arXiv2018

Near-Field Thermal Energy Conversion by Tunneling to a Waveguide

Energy is a vital resource and hence there is a continuous strive to improve upon existing technologies and to find new ones that address that basic need. The conversion of thermal energy is the primary method of generating electrical energy from a broad range of sources, for example fossil fuels, solar thermal, geothermal, and nuclear energy. A common need in all cases is the ability to efficiently extract the generated electromagnetic and thermal energy and to convert it to electricity. The current methods of thermal energy extraction are based on heat engines, thermoelectric and thermophotovoltaic conversion systems. In this report a method based on the direct extraction of Electromagnetic energy from the thermal near-field through tunneling and subsequent waveguiding, is presented.

cond-mat.mes-hall↗

arXiv2017

Probing the Hydrogen Enhanced Near-Field Emission of ITO without a Vacuum-Gap

Thermal fluctuations of charged particles, fluctuations akin to Brownian motion, can excite optical surface-states leading to the concept of the thermal near-field, which is a highly localized, and, therefore, evanescent optical density of states that exist at distances much less than the thermal emission wavelength. By tunneling the surface charge emitted photons into nearby waveguides, the thermally excitable near-field optical density of states can be enhanced, engineered, and efficiently extracted to the far-field for observation. With this technique, the plasmonic thermal near-field of a 10nm thick ITO film, known to have plasmonic activity in the 1500nm wavelength region, was probed under external illumination and by thermal excitation at 873K. The results confirm that waveguides provide a large density of optical channels with spatial overlap and k-vector matching to facilitate plasmon de-excitation in the near-field through photon tunneling for extraction into the far-field. Furthermore, it is shown that the thermal near-field can be observed without the introduction of a vacuum-gap, a feature unique to this particular method.

cond-mat.mes-hall↗