The lack of a sizeable
band gap has so far prevented graphene from
building effective electronic and optoelectronic devices despite its
numerous exceptional properties. Intensive theoretical research reveals
that a band gap larger than 1 eV can only be achieved in sub-3 nm
wide graphene nanoribbons (GNRs), but real fabrication of such ultranarrow
GNRs still remains a critical challenge. Herein, we demonstrate an
approach for the synthesis of ultranarrow and photoluminescent semiconducting
GNRs by longitudinally unzipping single-walled carbon nanotubes. Atomic
force microscopy reveals the unzipping process, and the resulting
2.2 nm wide GNRs are found to emit strong and sharp photoluminescence
at ∼685 nm, demonstrating a very desirable semiconducting nature.
This band gap of 1.8 eV is further confirmed by follow-up photoconductivity
measurements, where a considerable photocurrent is generated, as the
excitation wavelength becomes shorter than 700 nm. More importantly,
our fabricated GNR field-effect transistors (FETs), by employing the
hexagonal boron nitride-encapsulated heterostructure to achieve edge-bonded
contacts, demonstrate a high current on/off ratio beyond 105 and carrier mobility of 840 cm2/V s, approaching the
theoretical scattering limit in semiconducting GNRs at room temperature.
Especially, highly aligned GNR bundles with lengths up to a millimeter
are also achieved by prepatterning a template, and the fabricated
GNR bundle FETs show a high on/off ratio reaching 105,
well-defined saturation currents, and strong light-emitting properties.
Therefore, GNRs produced by this method open a door for promising
applications in graphene-based electronics and optoelectronics.