An automatic implantable cardiac defibrillator (AICD) is a device that is implanted in the chest to constantly monitor and, if necessary, correct episodes of arrhythmia. While the longevity of the average AICD patient has increased to 10 years after implantation, only 5% of implants functioned for seven years, and this mismatch poses a significant and ever growing clinical and economic burden. Moreover, there are now efforts to “piggyback” devices on AICDs and BVPs for additional functionality, all of which require more power. An innovative approach towards generating power for AICDs is to harness the energy of the heart by embedding energy generators in AICD leads. The cardiovascular system as a source generator is appealing due to its ability to continuously deliver mechanical energy as long as the patient is alive. Herein a device incorporating nanostructured piezoelectrics was developed as a means to harvest the energy of heart. The generator system integrates inorganic piezoelectric nanomaterials, including aligned arrays of nanowires of crystalline zinc oxide (ZnO), with elastomeric substrates. The design combines several innovative structural configurations including a “wavy” flexible electrode and a layout where the nanowires are near or on the neutral mechanical plane. A wet synthetic strategy to reliably prepare piezoelectric ZnO nanostructures directly onto the devices was also developed and optimized to produce nanowires with high densities, large aspect ratios and high orientation. The elastomeric support permits direct integration within AICD leads and is small and flexible enough to not add resistance in systole. The flexible devices were integrated into a testbed mimicking the input a failing right ventricle and the results demonstrate progress towards energy harvesting from the cardiovascular system. A model was developed to gain insight as to how to structure the nanowire array within the latitude of the synthesis to boost the energy production. To further improve the output, the nanowires were passivated with dipolar molecules to change their resistivities and the barrier height of the Schottky contact. A novel low photon energy photoelectron spectroscopy tool was developed to measure the effects of the molecules on the individual nanowire properties. This concept of using nanostructured piezoelectrics as a means to convert the energy of the body may in the coming years represent a paradigm shift from battery dependant AICD modules to completely autonomous functional systems. / text

FePt/B4C multilayer thin films are deposited on silicon substrates using magnetron sputtering with different B4C layer thickness. Experimental results suggest that the B4C layers effectively serve as spacers to separate the FePt layers, making the multilayer configuration stable even after film annealing at elevated temperatures. On the other hand, B and C are found to be incorporated into the FePt layer, which is responsible for the FePt grain growth confinement and grain separation, and eventually affects the properties of the composite film. Based on the experimental results of multilayer composite film, particle (FePt)/matrix (B4C) monolayer composite thin films on Si substrate are synthesized, in which a record coercivity of 2200 Oe is achieved compared to similar system. The size uniformity of the FePt nanoparticles, the well-defined particle-particle separation, together with the good magnetic property and high temperature thermal stability of the overall composite film, make it a very promising candidate for the ultrahigh density magnetic storage media. / Functional nanostructures serve as the basic building blocks for nanodevices and significant efforts have been devoted to their morphology control and properties optimization. In present study, four functional nanostructures, i.e., FePt/B4C multilayer composite film, particle (FePt)/matrix (B4C) monolayer composite film, Ga-doped ZnO nanowire arrays, and CdSe nanotube arrays are designed, synthesized and characterized in detail, in which the first two are expected to be prominent candidates for ultrahigh-density magnetic storage media while the later two have potential applications in solar energy conversion. / Semiconductor based one-dimensional nanostructures are investigated as promising building blocks for solar energy conversion devices. Two aspects are explored, aiming at increasing the energy conversion efficiency, i.e., facilitating electron transport and enhancing photon absorbing. In the first case, large area Ga-doped ZnO nanowire arrays are grown on transparent conducting substrate. Experimental results reveal the well-aligned array morphology and the uniform Ga concentration in these nanowires. In particular, direct I-V measurements performed on single nanowire-on-ITO substrate disclose its Ohmic contact with the conducting substrate and the significant conductivity improvement compared to undoped ZnO nanowire, In the second case, a novel synthesis strategy for nanotube arrays is developed and CdSe is used for demonstration, which material possessing more appropriate band gap as effective light harvester compared to that of materials for existing semiconductor nanotube arrays. The controllable tube wall thickness that can be increased until continuous CdSe porous network is obtained. The experimental results suggest a nanotube array formation mechanism that can be generally applied to a wide range of materials. / Zhou, Minjie = 功能纳米结构在磁性和能源方面的应用 / 周民杰. / Adviser: Li Quan. / Source: Dissertation Abstracts International, Volume: 72-11, Section: B, page: . / Thesis (Ph.D.)--Chinese University of Hong Kong, 2009. / Includes bibliographical references (leaves 91-100). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [201-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Abstract also in Chinese. / Zhou, Minjie = Gong neng na mi jie gou zai ci xing he neng yuan fang mian de ying yong / Zhou Minjie.