Block copolymer self-assembly–directed synthesis of mesoporous gyroidal superconductors

Block copolymer self-assembly is used to synthesize three-dimensionally continuous gyroidal mesoporous superconductors of niobium nitride. Superconductors with periodically ordered mesoporous structures are expected to have properties very different from those of their bulk counterparts. Systematic...

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Published inScience advances Vol. 2; no. 1; p. e1501119
Main Authors Robbins, Spencer W., Beaucage, Peter A., Sai, Hiroaki, Tan, Kwan Wee, Werner, Jörg G., Sethna, James P., DiSalvo, Francis J., Gruner, Sol M., Van Dover, Robert B., Wiesner, Ulrich
Format Journal Article
LanguageEnglish
Published United States AAAS 01.01.2016
American Association for the Advancement of Science
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Summary:Block copolymer self-assembly is used to synthesize three-dimensionally continuous gyroidal mesoporous superconductors of niobium nitride. Superconductors with periodically ordered mesoporous structures are expected to have properties very different from those of their bulk counterparts. Systematic studies of such phenomena to date are sparse, however, because of a lack of versatile synthetic approaches to such materials. We demonstrate the formation of three-dimensionally continuous gyroidal mesoporous niobium nitride (NbN) superconductors from chiral ABC triblock terpolymer self-assembly–directed sol-gel–derived niobium oxide with subsequent thermal processing in air and ammonia gas. Superconducting materials exhibit a critical temperature ( T c ) of about 7 to 8 K, a flux exclusion of about 5% compared to a dense NbN solid, and an estimated critical current density ( J c ) of 440 A cm −2 at 100 Oe and 2.5 K. We expect block copolymer self-assembly–directed mesoporous superconductors to provide interesting subjects for mesostructure-superconductivity correlation studies.
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USDOE Office of Science (SC), Basic Energy Sciences (BES)
SC0001086; FG02-11ER16210
These authors contributed equally to this work.
Present address: Low Energy Electronic Systems IRG, Singapore-MIT Alliance for Research and Technology, Singapore 138602, Singapore.
Present address: Simpson Querrey Institute for Bionanotechnology, Northwestern University, Evanston, IL 60208, USA.
ISSN:2375-2548
2375-2548
DOI:10.1126/sciadv.1501119