We report the synthesis and systematic Raman study of twisted bilayer graphene (tBLG) with rotation angles from below 10° to nearly 30°. Chemical vapor deposition was used to grow hexagon-shaped tBLG with a rotation angle that can be conveniently determined by relative edge misalignment. Rotation dependent G-line resonances and folded phonons were observed by selecting suitable energies of excitation lasers. The observed phonon frequencies of the tBLG superlattices agree well with our ab initio calculation.

Highly crystalline and emissive carbon dots (CDs) are firstly synthesized via an ionothermal method in organic solvents. ZnCl 2 is utilized as the pyrolysispromoting agent to prepare emissive CDs with tunable wavelengths, directly by carbonization from different O and N precursors under a mild reaction condition. Excellent synthetic yield and photoluminescent quantum yield are obtained. The resulting CDs exhibit excellent capability to photogenerate superoxide radical anion (O 2 ,-), which can be exemplified by both photodynamic therapy and photooxidative cyclization reactions.

Quantum technologies require robust and photostable single-photon emitters. Here, room temperature operated single-photon emissions from isolated defects in aluminum nitride (AlN) films are reported. AlN films were grown on nanopatterned sapphire substrates by metal organic chemical vapor deposition. The observed emission lines range from visible to near-infrared, with highly linear polarization characteristics. The temperature-dependent line width increase shows T3 or single-exponential behavior. First-principle calculations based on density functional theory show that point defect species, such as antisite nitrogen vacancy complex (NAlVN) and divacancy (VAlVN) complexes, are considered to be an important physical origin of observed emission lines ranging from approximately 550 to 1000 nm. The results provide a new platform for on-chip quantum sources.

Symmetric and nonsymmetric diarylethenes with a 2,5-dihydropyrrole bridging unit have been prepared, and the photochromic properties are investigated. Both symmetric and nonsymmetric diarylethenes with 2,5-dihydropyrrole bridging units undergo reversible ring-opening and ring-closing photoisomerization reactions in nonpolar solvents with UV/vis light, and some of them exhibit good fatigue resistance and no marked degradation detected after 10 cycles via an on/off switch. In polar solvents, however, photochromic diarylethenes with 2,5-dihydropyrrole bridging units produce 3,4-diarylpyrrole derivatives instead of the ring-closing isomer of diarylethenes with UV light irradiation. A class of N-substituted 3,4-diphenylethenes with 2,5-dihydropyrrole bridging units were prepared and used as templates to investigate the conversion reactions. The mechanism of photoconversion of 3,4-diaryl-2,5-dihydropyrroles to 3,4-diarylpyrroles was explored as well.