posted on 2022-04-07, 19:41authored byZiyi Hu, Ben Breeze, Reza J. Kashtiban, Jeremy Sloan, James Lloyd-Hughes
Atomically thin nanowires
(NWs) can be synthesized inside single-walled
carbon nanotubes (SWCNTs) and feature unique crystal structures. Here
we show that HgTe nanowires formed inside small-diameter (<1 nm)
SWCNTs can advantageously alter the optical and electronic properties
of the SWCNTs. Metallic purification of the filled SWCNTs was achieved
by a gel column chromatography method, leading to an efficient extraction
of the semiconducting and metallic portions with known chiralities.
Electron microscopic imaging revealed that zigzag HgTe chains were
the dominant NW geometry in both the semiconducting and metallic species.
Equilibrium-state and ultrafast spectroscopy demonstrated that the
coupled electron–phonon system was modified by the encapsulated
HgTe NWs, in a way that varied with the chirality. For semiconducting
SWCNTs with HgTe NWs, Auger relaxation processes were suppressed,
leading to enhanced photoluminescence emission. In contrast, HgTe
NWs enhanced the Auger relaxation rate of metallic SWCNTs and created
faster phonon relaxation, providing experimental evidence that encapsulated
atomic chains can suppress hot carrier effects and therefore boost
electronic transport.