| 1. |
- Kim, Kyung Ho, 1984, et al.
(författare)
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Ambipolar charge transport in quasi-free-standing monolayer graphene on SiC obtained by gold intercalation
- 2020
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Ingår i: Physical Review B. - : American Physical Society. - 2469-9950 .- 2469-9969. ; 102:16
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Tidskriftsartikel (refereegranskat)abstract
- We present a study of quasi-free-standing monolayer graphene obtained by intercalation of Au atoms at the interface between the carbon buffer layer (Bu-L) and the silicon-terminated face (0001) of 4H-silicon carbide. Au intercalation is achieved by deposition of an atomically thin Au layer on the Bu-L followed by annealing at 850 °C in an argon atmosphere. We explore the intercalation of Au and decoupling of the Bu-L into quasi-free-standing monolayer graphene by surface science characterization and electron transport in top-gated electronic devices. By gate-dependent magnetotransport we find that the Au-intercalated buffer layer displays all properties of monolayer graphene, namely gate-tunable ambipolar transport across the Dirac point, but we find no observable enhancement of spin-orbit effects in the graphene layer, despite its proximity to the intercalated Au layer.
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| 2. |
- Kim, Kyung Ho, 1984, et al.
(författare)
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Chemical Sensing with Atomically Thin Platinum Templated by a 2D Insulator
- 2020
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Ingår i: Advanced Materials Interfaces. - : Wiley. - 2196-7350. ; 7:12
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Tidskriftsartikel (refereegranskat)abstract
- Boosting the sensitivity of solid‐state gas sensors by incorporating nanostructured materials as the active sensing element can be complicated by interfacial effects. Interfaces at nanoparticles, grains, or contacts may result in nonlinear current–voltage response, high electrical resistance, and ultimately, electric noise that limits the sensor read‐out. This work reports the possibility to prepare nominally one atom thin, electrically continuous platinum layers by physical vapor deposition on the carbon zero layer (also known as the buffer layer) grown epitaxially on silicon carbide. With a 3–4 Å thin Pt layer, the electrical conductivity of the metal is strongly modulated when interacting with chemical analytes, due to charges being transferred to/from Pt. The strong interaction with chemical species, together with the scalability of the material, enables the fabrication of chemiresistor devices for electrical read‐out of chemical species with sub part‐per‐billion (ppb) detection limits. The 2D system formed by atomically thin Pt on the carbon zero layer on SiC opens up a route for resilient and high sensitivity chemical detection, and can be the path for designing new heterogenous catalysts with superior activity and selectivity.
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| 3. |
- Sheng, C. X., et al.
(författare)
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Ultrafast Transient Spectroscopy of Trans-Polyacetylene in the Midinfrared Spectral Range
- 2020
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Ingår i: Physical Review Letters. - 1079-7114 .- 0031-9007. ; 124:1
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Tidskriftsartikel (refereegranskat)abstract
- Trans-polyacetylene [t-(CH)(x)] possesses twofold ground state degeneracy. Using the Su-Schrieffer-Heeger Hamiltonian, scientists predicted charged solitons to be the primary photoexcitations in t-(CH)(x); this prediction, however, has led to sharp debate. To resolve this saga, we use subpicosecond transient photomodulation spectroscopy in the mid-IR spectral range (0.1-1.5 eV) in neat t-(CH)(x) thin films. We show that odd-parity singlet excitons are the primary photoexcitations in t-(CH)(x), similar to many other nondegenerate pi-conjugated polymers. The exciton transitions are characterized by two photoinduced absorption (PA) bands at 0.38 and 0.6 eV, and an associated photoluminescence band at similar to 1.5 eV having similar polarization memory. The primary excitons undergo internal conversion within similar to 100 fs to an even parity (dark) singlet exciton with a PA band at similar to 1.4 eV. We also find ultrafast photogeneration of charge polarons when pumping deep into the polymer continuum band, which are characterized by two other PA bands in the mid-IR and associated photoinduced IR vibrational modes.
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