The direct electrodeposition of crystalline ger
maniu
m (Ge) nanowire fil
m electrodes fro
m an aqueous solution of dissolved GeO
2 using discrete 鈥榝lux鈥?nanoparticles capable of dissolving Ge(s) has been de
monstrated. Electrodeposition of Ge at inert electrode substrates decorated with s
mall (<100 n
m), discrete indiu
m (In) nanoparticles resulted in crystalline Ge nanowire fil
ms with definable nanowire dia
meters and densities without the need for a physical or che
mical te
mplate. The Ge nanowires exhibited strong polycrystalline character as-deposited, with approxi
mate crystallite di
mensions of 20 n
m and a
mixed orientation of the crystallites along the length of the nanowire. Energy dispersive spectroscopic ele
mental
mapping of individual Ge nanowires showed that the In nanoparticles re
mained at the base of each nanowire, indicating good electrical co
mmunication between the Ge nanowire and the underlying conductive support. As-deposited Ge nanowire fil
ms prepared on Cu supports were used without further processing as Li
+ battery anodes. Cycling studies perfor
med at 1 C (1624
mA g
鈥?) indicated the native Ge nanowire fil
ms supported stable discharge capacities at the level of 973
mA h g
鈥?, higher than analogous Ge nanowire fil
m electrodes prepared through an energy-intensive vapor鈥搇iquid鈥搒olid nanowire growth process. The cu
mulative data show that ec-LLS is a viable
method for directly preparing a functional, high-activity nano
materials-based device co
mponent. The work presented here is a step toward the realization of si
mple processes that
make fully functional energy conversion/storage technologies based on crystalline inorganic se
miconductors entirely through benchtop, aqueous che
mistry and electroche
mistry without ti
me- or energy-intensive process steps.
Keywords:
manium+nanowires&qsSearchArea=searchText">Germanium nanowires; ec-LLS; electrodeposition; m%5C-ion+battery+anodes&qsSearchArea=searchText">lithium-ion battery anodes