The widespread popularity of lithium-ion full batteries
(LIFBs)
has gradually demonstrated the need for fast charge and discharge.
In this article, the application of microporous copper foil current
collector (MC) and microporous aluminum foil current collector (MA)
prepared by electrolytic etching in ultra-high rate LIFBs was studied.
Compared with conventional copper foil current collectors (CC) and
aluminum foil current collectors (CA), MC–MA has better electrical
performance and safety performance in an ultra-high-rate system. The
pore size of MC is mainly distributed in 2–10 μm, and
MA is mainly distributed in 1–15 μm. Scanning electron
microscope shows that the pore structure on MC–MA is a disordered
pore. The formation of micropores weakens mechanical strength and
elongation of the current collector. The strength of copper foil before
and after pore-forming decreased from 317.77 to 305.21 MPa, and the
elongation decreased from 5.4 to 2.26%. The strength of aluminum foil
before and after pore-forming decreased from 287.24 to 237.83 MPa,
and the elongation decreased from 3.16 to 1.74%. However, there was
no significant change in the thickness and areal density before and
after pore-forming. The formation of micropores increases the three-dimensional
interface contact sites of the current collector, thereby improving
adhesion strength and reducing the resistivity of the electrode. However,
too many contact interfaces also face more side reactions, which also
cause the self-discharge and high-temperature storage of MC–MA
(0.033) to be slightly worse than that of CC–CA (0.030). The
electrochemical results show that MC–MA has a larger specific
capacity, better rate performance, and lower electrochemical impedance.
The capacity retentions of MC–MA after 500 cycles at 5C and
10C were 84.81 and 76.96% and CC–CA were 81.85 and 62.43%,
respectively. The capacity retentions of MC–MA and CC–CA
are 84.20 and 73.78% after 500 cycles at 5C charge and 15C pulse discharge.
The cell disassembly found that lithium dendrites were the main cause
of the capacity decay. The excellent three-dimensional interface of
micropore provides more reaction sites, and two-dimensional surface
defects reduce current density distribution and realize uniform distribution
of lithium ions at different phase interfaces. The micropore provides
stress release space for volume expansion of charge and discharge
and improves voltage hysteresis caused by compressive stress at the
interface between the current collector and materials coating. In
addition, due to pore structure changes in the elastic deformation
ability and surface current density distribution of the current collector,
the safety performance of LIFBs is improved.