Nanoimprinted substrates for high-yield production of topological insulator nanoribbons

We present a growth process mediated by nanoimprinted nanostructures specifically for producing bismuth selenide (Bi₂Se₃) topological insulator nanoribbons with a high yield. In this process, topological insulator nanostructures are grown on nanoimprinted gratings by using a nanoparticle-catalyzed vapor–liquid–solid mechanism. In comparison with the growth processes performed on flat and randomly rough substrates, such a nanograting-mediated growth method produces topological insulator nanoribbons with a higher yield (～15?000 nanoribbons/mm²), a narrower average ribbon width (w _avg<60 nm), and a higher uniformity in ribbon width (σ<30 nm); effectively suppresses the formation of other unwanted morphologies; and also results in the axial growth of nanoribbons along specific in-plane directions relative to pre-structured gratings. Such technical merits of nanograting-mediated growth are attributed to the preferential nucleation of Bi₂Se₃ crystal seeds and the concomitant pinning of catalytic nanoparticles at ordered grating edges. Finally, Aharonov–Bohm interference oscillations in the magnetoresistance were observed and demonstrated the coherent transport of electrons through topological surface states of Bi₂Se₃ nanoribbons. This growth process in combination with large-area nanoimprint lithography could serve as an important foundation for nanomanufacturing topological insulator nanoribbons with controllable feature size, large-area uniformity, and ordering, suitable for applications in future low-dissipation nanoelectronics.     

Reactivity of cyano- and isothiocyanatoborylenes: metal coordination,one-electron oxidation and boron-centred Brønsted basicity

Doubly base-stabilised cyano- and isothiocyanatoborylenes of the form LL′BY (L = CAAC = cyclic alkyl(amino)carbene; L′ = NHC = N-heterocyclic carbene; Y = CN, NCS) coordinate to group 6 carbonyl complexes via the terminal donor of the pseudohalide substituent and undergo facile and fully reversible one-electron oxidation to the corresponding boryl radical cations [LL′BY]˙⁺. Furthermore, calculations show that the borylenes have very similar proton affinities, both to each other and to NHC superbases. However, while the protonation of LL′B(CN) with PhSH yielding [LL′BH(CN)⁺][PhS⁻] is fully reversible, that of LL′B(NCS) is rendered irreversible by a subsequent B-to-C_CAAC hydrogen shift and nucleophilic attack of PhS⁻ at boron.

Borylenes of the form (CAAC)(NHC)BY (Y = CN, NCS; CAAC = cyclic alkyl(amino)carbene; NHC = N-heterocyclic carbene) coordinate to group 6 carbonyl complexes via Y, and show reversible boron-centered Brønsted basicity and one-electron oxidation.