We des
cribe the fabri
cation of arrays of nanowires on glass in whi
ch a gold
core nanowire is en
capsulated within a hemi
cylindri
cal shell of manganese dioxide. Arrays of linear gold (Au) nanowires are first prepared on glass using the lithographi
cally patterned nanowire ele
ctrodeposition (LPNE) method. These Au nanowires have a re
ctangular
cross-se
ction with a width and height of 鈮?00 and 40 nm, respe
ctively, and lengths in the 1 mm to 1
cm range. Au nanowires are then used to deposit MnO
2 by potentiostati
c ele
ctrooxidation from Mn
2+ solution, forming a
conformal, hemi
cylindri
cal shell with a
controllable diameter ranging from 50 to 300 nm surrounding ea
ch Au nanowire. This MnO
2 shell is 未-phase and mesoporous, as revealed by X-ray diffra
ction and Raman spe
ctros
copy. Transmission ele
ctron mi
cros
copy (TEM) analysis reveals that the MnO
2 shell is mesoporous (
mp-MnO
2),
consisting of a network of 鈮? nm fibrils. The spe
cifi
c capa
citan
ce,
Csp, of arrays of gold:
mp-MnO
2 nanowires is measured using
cy
cli
c voltammetry. For a
mp-MnO
2 shell thi
ckness of 68 卤 3 nm,
core:shell nanowires produ
ce a
Csp of 1020 卤 100 F/g at 5 mV/s and 450 卤 70 F/g at 100 mV/s. The
cy
cle stability of this
Csp, however, is extremely limited in aqueous ele
ctrolyte, de
caying by >90% in 100 s
cans, but after oven drying and immersion in dry 1.0 M LiClO
4, a
cetonitrile, dramati
cally improved
cy
cle stability is a
chieved
chara
cterized by the absen
ce of
Csp fade for 1000
cy
cles at 100 mV/s. Core:shell nanowires exhibit true hybrid energy storage, as revealed by de
convolution of
Csp into insertion and noninsertion
components.
Keywords:
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