The ε-LiVOPO4 cathode for Li-ion batteries
has
attracted wide attention with its multivalent electronic states and
improved discharge capacity of over 300 mAh/g. Oxygen loss stands
as a potential cause for structural degradations of the ε-LiVOPO4 cathode and its derivatives but has been barely studied.
Through in situ environmental transmission electron
microscopy, we probe lattice oxygen loss and the associated structural
degradations by spatially and temporally resolving the atomic-scale
structural dynamics and phase transformation pathways in ε-LiVOPO4. We demonstrate that the mild oxygen loss at 400 °C
induces a topotactic phase transformation of ε-LiVOPO4 → α-Li3V2(PO4)3 in the particle surface via a nucleation and growth mechanism,
leading to the formation of a core–shell configuration. The
phase transformation can be reversed by switching to an oxidizing
environment, in which the α-Li3V2(PO4)3 is reoxidized to ε-LiVOPO4.
By contrast, oxygen loss at higher temperatures of 500 and 600 °C
results in a high concentration of oxygen vacancies that subsequently
induces irreversible structural damages including lattice amorphization
and formation of nanocavities. This work illustrates the fundamental
mechanisms governing the structural failure of oxide cathodes and
underlines possible strategies to overcome such issues by exploiting
environmental constraints