2 research outputs found
Insight on the Failure Mechanism of Sn Electrodes for Sodium-Ion Batteries: Evidence of Pore Formation during Sodiation and Crack Formation during Desodiation
The
development of Sn based anode materials for sodium ion batteries
is mainly hindered by the limited understanding of sodiation/desodiation
mechanisms inside the active material, which typically results in
electrode damage. Herein, we report a post-mortem ex-situ scanning
electron microscopic analysis of Sn thin film motivated by the intention
to elucidate these structural mechanisms. Our results reveal for the
first time that the surface of Sn electrode film becomes highly porous
during sodiation with no presence of obvious cracks, a surprising
result when compared to previous reports performed on Sn particles.
Even more surprisingly, sequential ex-situ SEM observations demonstrate
that, once the desodiation starts and reaches the second desodiation
plateau (0.28 V), obvious cracks in the Sn film are instead observed
along with porous islands of active material. These islands appear
as aggregated particles which further split into smaller islands when
the desodiation potential reaches its maximum value (2.0 V). Finally,
for the first time, the experimental value of the sodium diffusion
coefficient inside Sn was measured (3.9 × 10–14 cm2 s–1) using electrochemical impedance
spectroscopy
Direct Synthesis of Carbon-Doped TiO<sub>2</sub>–Bronze Nanowires as Anode Materials for High Performance Lithium-Ion Batteries
Carbon-doped TiO<sub>2</sub>–bronze
nanowires were synthesized via a facile doping mechanism and were
exploited as active material for Li-ion batteries. We demonstrate
that both the wire geometry and the presence of carbon doping contribute
to the high electrochemical performance of these materials. Direct
carbon doping for example reduces the Li-ion diffusion length and
improves the electrical conductivity of the wires, as demonstrated
by cycling experiments, which evidenced remarkably higher capacities
and superior rate capability over the undoped nanowires. The as-prepared
carbon-doped nanowires, evaluated in lithium half-cells, exhibited
lithium storage capacity of ∼306 mA h g<sup>–1</sup> (91% of the theoretical capacity) at the current rate of 0.1<i>C</i> as well as excellent discharge capacity of ∼160
mAh g<sup>–1</sup> even at the current rate of 10 C after 1000
charge/discharge cycles
