AVS 59th Annual International Symposium and Exhibition
    Energy Frontiers Focus Topic Thursday Sessions
       Session EN+NS-ThM

Paper EN+NS-ThM6
Engineering LixAlySizO Ionic Conductive Thin Films by Atomic Layer Deposition for Lithium-ion Battery Applications

Thursday, November 1, 2012, 9:40 am, Room 15

Session: Batteries and Fuel Cells
Presenter: Y.-C. Perng, University of California, Los Angeles
Authors: Y.-C. Perng, University of California, Los Angeles
J. Cho, University of California, Los Angeles
D. Membreno, University of California, Los Angeles
N. Cirigliano, University of California, Los Angeles
B. Dunn, University of California, Los Angeles
J.P. Chang, University of California, Los Angeles
Correspondent: Click to Email

Lithium (Li)-ion batteries have drawn much attention for their outstanding performance in portable electronics applications with the potentials to function as a power source for further minizaturized devices, including micro-systems through the utilization of 3-dimensional electrodes based on high aspect ratio pillars. To realize this potential, an ultra-thin and highly conformal electrolyte layer is needed to coat the 3D electrode array. The ionic conductor lithium aluminosilicate (LiAlSiO4) synthesized by atomic layer deposition (ALD) is a promising electrolyte material for 3D battery applications not only due to its high ionic conductivity along its c-axis resulting from channels formed by the alternating tetrahedra of aluminum-oxygen (Al-O) and silicon-oxygen (Si-O), but also expected to provide similar improved cell cyclability, as reported in the preliminary studies of ultra-thin metal-oxide ALD coatings on electrodes.

The self-limiting characteristic of ALD allows for precise control of thickness and composition of complex oxides and results in a highly conformal and pinhole-free coating suitable in 3D micro-battery applications or electrolyte surface coatings. The metal precursors used in this work are tetraethyl orthosilicate (TEOS), trimethylaluminum (TMA) and lithium t-butoxide (LTB). These precursors, along with water vapor as the oxidant, were used to deposit SiO2, Al2O3 and Li2O, with the deposition rates in the range of 0.8~2Å/cycle, respectively. The deposition rate of stoichiometric LiAlSiO4 was ~20Å/cycle at a temperature of 290°C. The concentration of each metal element in LixAlySizO (LASO) thin films was found to correlate closely to ALD cycles and the associated incubation times. The crystallinity of the films after post-deposition rapid thermal annealing (RTA) was a function of cation atomic percentage. Li-ionic conductivities and the activation energy of as-deposited LASO films with respect to lithium contents as well as their relation to the film thickness were studied. The LASO ALD coating on 3D features, such as NWs and nanopaticles (NPs), were confirmed to be conformal and uniform by transmission electron microscopy (TEM) imaging. The cell performance as well as cyclability enhancement from LixAlySizO was investigated for a silicon-nanowire 3D microbattery, where SiNW was used as an anode, to explore the potentials of a solid-state SiNW battery with a solid-oxide electrolyte.