Electrodes composed of silicon nanoparticles (SiNP) were prepared by slurry casting and then electrochemically tested in a fluoroethylene carbonate (FEC)-based electrolyte. The capacity retention after cycling was significantly improved compared to electrodes cycled in a traditional ethylene carbonate (EC)-based electrolyte.

Hydrothermally synthesized single-crystalline hematite (α-Fe 2 O 3 ) nanorods were investigated as an anode material for Li-ion batteries. Electrodes prepared with this material exhibited initial reversible capacities of 908 mAh g À1 at 0.2 C rate and 837 mAh g À1 at 0.5 C rate, and these capacities were completely retained after numerous cycles. The α-Fe 2 O 3 nanorods average ∼40 nm in diameter and ∼400 nm in length providing a short path for lithium-ion diffusion and effective accommodation of the strain generated from volume expansion during the lithiation/delithiation process.

Both silicon and germanium are leading candidates to replace the carbon anode of lithium ions batteries. Silicon is attractive because of its high lithium storage capacity while germanium, a superior electronic and ionic conductor, can support much higher charge/discharge rates. Here we investigate the electronic, electrochemical and optical properties of Si(1-x)Gex thin films with x = 0, 0.25, 0.5, 0.75, and 1. Glancing angle deposition provided amorphous films of reproducible nanostructure and porosity. The film's composition and physical properties were investigated by X-ray photoelectron spectroscopy, four-point probe conductivity, Raman, and UV-vis absorption spectroscopy. The films were assembled into coin cells to test their electrochemical properties as a lithium-ion battery anode material. The cells were cycled at various C-rates to determine the upper limits for high rate performance. Adjusting the composition in the Si(1-x)Gex system demonstrates a trade-off between rate capability and specific capacity. We show that high-capacity silicon anodes and high-rate germanium anodes are merely the two extremes; the composition of Si(1-x)Gex alloys provides a new parameter to use in electrode optimization.

Both nanocolumnar and dense germanium thin films, synthesized by evaporative deposition, were tested as a potential anode material for sodium-ion batteries. The reversible capacity of the nanocolumnar films was found to be 430 mAh/g, which is higher than the theoretical capacity of 369 mAh/g. The nanocolumnar films retained 88% of their initial capacity after 100 cycles at C/5, whereas the dense films began to deteriorate after ∼15 cycles. Additionally, the nanocolumnar films were stable at charge/discharge rates up to 27C (10 A/g). The diffusion coefficient for sodium in germanium was estimated, from impedance analysis of the dense films, to be ∼10 −13 cm 2 s −1 . Modeling of diffusion in the sodium-germanium system predicts that sodium diffusion in the near-surface layers of the material is significantly faster than in the bulk. These results show that small feature sizes are critical for rapid, reversible electrochemical sodiation of germanium.

Silicon and partially oxidized silicon thin films with nanocolumnar morphology were synthesized by evaporative deposition at a glancing angle, and their performance as lithium-ion battery anodes was evaluated. The incorporated oxygen concentration was controlled by varying the partial pressure of water during the deposition and monitored by quartz crystal microbalance, X-ray photoelectron spectroscopy. In addition to bulk oxygen content, surface oxidation and annealing at low temperature affected the cycling stability and lithium-storage capacity of the films. By simultaneously optimizing all three, films of ~2200 mAh/g capacity were synthesized. Coin cells made with the optimized films were reversibly cycled for ~120 cycles with virtually no capacity fade. After 300 cycles, 80% of the initial reversible capacity was retained.