The use of high capacity electrode
materials based on alloying
and dealloying reactions with Na is very effective for improving energy
density of batteries. However, their application brings on electrical
isolation such as detachment of the electrode mixture layer from a
current collector, causing rapid capacity fading. We previously found
that Cu electrochemically grows in sheet form by electroplating in
a CuSO4-based aqueous solution with poly(acrylic acid)
(PAA). In the present study, our goal was to elucidate the formation
mechanism of Cu sheets by characterization using scanning transmission
electron microscopy (STEM), X-ray diffraction (XRD) analysis, and
electron scatter diffraction patterns (EBSD) mapping. Then, the cycling
performance of a Sn negative electrode for Na-ion batteries was significantly
upgraded by the application of a roughened-Cu substrate with optimized
sheet thickness. The STEM images and EBSD maps revealed that the Cu
sheet was a single crystal, and the results obtained from XRD and
the cathodic polarization behavior of Cu electrodeposition in PAA-containing
solutions suggested that PAA molecules adsorbed onto Cu (100) to suppress
the Cu growth on the plane, resulting in the formation of Cu sheets.
Although the initial reversible capacities of flat-Cu/Sn and roughened-Cu/Sn
electrodes were comparable, the developed Cu substrate (1.0 ×
10–4 M PAA) delivered a noticeable increase in the
reversible capacity by 210 mA h g–1 from the first
to the second cycle, whereas the flat-Cu remained the increase by
100 mA h g–1. In addition, the roughened-Cu substrate
suppressed the detachment of the active material layer to maintain
a high capacity of 685 mA h g–1 with good capacity
retention of more than 90% by the anchor effect. These results demonstrate
that the roughened-Cu substrate prepared in the present work is a
promising candidate as a current collector for rechargeable batteries.