Unzipping multiwall carbon nanotubes (MWCNTs) attracted great interest as a method for producing graphene nanoribbons (GNRs). However, depending on the production method, the GNRs have been proposed to form by different mechanisms. Here, we demonstrate that the oxidative unzipping of MWCNTs is intercalation-driven, not oxidative chemical-bond cleavage as was formerly proposed. The unzipping mechanism involves three consecutive steps: intercalation-unzipping, oxidation, and exfoliation. The reaction can be terminated at any of these three steps. We demonstrate that even in highly oxidative media one can obtain nonoxidized GNR products. The understanding of the actual unzipping mechanism lets us produce GNRs with hybrid properties varying from nonoxidized through heavily oxidized materials. We answer several questions such as the reason for the innermost walls of the nanotubes remaining zipped. The intercalation-driven reaction mechanism provides a rationale for the difficulty in unzipping single-wall and few-wall CNTs and aids in a reevaluation of the data from the oxidative unzipping process.
Single crystals of the ternary iron selenide RbFeSe 2 have been investigated by means of x-ray diffraction, magnetic susceptibility, magnetization, and specific-heat measurements as well as by Mössbauer spectroscopy. Built up from linear chains of edge-sharing FeSe 4 tetrahedra, RbFeSe 2 represents a quasi-one-dimensional antiferromagnet. Below T N = 248 K three-dimensional antiferromagnetic collinear magnetic order sets in, with the magnetic moments oriented perpendicularly to the chain direction. The hyperfine fields determined from our Mössbauer studies reveal strongly reduced magnetic moments. The high-temperature susceptibility data of RbFeSe 2 suggest a one-dimensional metallic character along the chains.
SrEr 2 O 4 is a geometrically frustrated magnet which demonstrates rather unusual properties at low temperatures including a coexistence of long-and short-range magnetic order, characterized by two different propagation vectors. In the present work, the effects of crystal fields (CFs) in this compound containing four magnetically inequivalent erbium sublattices are investigated experimentally and theoretically. We combine the measurements of the CF levels of the Er 3+ ions made on a powder sample of SrEr 2 O 4 using neutron spectroscopy with site-selective optical and electron paramagnetic resonance measurements performed on single-crystal samples of the lightly Er-doped nonmagnetic analog, SrY 2 O 4 . Two sets of CF parameters corresponding to the Er 3+ ions at the crystallographically inequivalent lattice sites are derived which fit all the available experimental data well, including the magnetization and dc susceptibility data for both lightly doped and concentrated samples.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.