A modular synthetic approach for band-gap engineering of armchair graphene nanoribbons
暂无分享,去创建一个
Gang Li | Guangbin Dong | J. Wen | X. Zhu | J. Guest | Rui Zhang | Ki-Young Yoon | Jianchun Wang | Xinjue Zhong
[1] M. Turner,et al. Borylated Arylamine–Benzothiadiazole Donor–Acceptor Materials as Low-LUMO, Low-Band-Gap Chromophores , 2017 .
[2] T. Herng,et al. Rylene Ribbons with Unusual Diradical Character , 2017 .
[3] Dongqing Wu,et al. Poly(ethylene oxide) Functionalized Graphene Nanoribbons with Excellent Solution Processability. , 2016, Journal of the American Chemical Society.
[4] M. Tommasini,et al. Bottom-Up Synthesis of Soluble and Narrow Graphene Nanoribbons Using Alkyne Benzannulations. , 2016, Journal of the American Chemical Society.
[5] T. Michinobu,et al. Benzothiadiazole and its π-extended, heteroannulated derivatives: useful acceptor building blocks for high-performance donor–acceptor polymers in organic electronics , 2016 .
[6] Gang Li,et al. Efficient Bottom-Up Preparation of Graphene Nanoribbons by Mild Suzuki-Miyaura Polymerization of Simple Triaryl Monomers. , 2016, Chemistry.
[7] G. M. e Silva,et al. Polaron Properties in Armchair Graphene Nanoribbons. , 2016, The journal of physical chemistry. A.
[8] A. Ferrari,et al. Raman Fingerprints of Atomically Precise Graphene Nanoribbons , 2016, Nano letters.
[9] Kenichiro Itami,et al. Structurally uniform and atomically precise carbon nanostructures , 2016 .
[10] Ari Harju,et al. Ultra-narrow metallic armchair graphene nanoribbons , 2015, Nature Communications.
[11] K. Müllen,et al. New advances in nanographene chemistry. , 2015, Chemical Society reviews.
[12] M. Turner,et al. Enhancing electron affinity and tuning band gap in donor–acceptor organic semiconductors by benzothiadiazole directed C–H borylation , 2015, Chemical science.
[13] K. Sun,et al. On-surface synthesis of rylene-type graphene nanoribbons. , 2015, Journal of the American Chemical Society.
[14] K. Müllen,et al. Bottom-up synthesis of chemically precise graphene nanoribbons. , 2015, Chemical record.
[15] Ting Cao,et al. Molecular bandgap engineering of bottom-up synthesized graphene nanoribbon heterojunctions. , 2015, Nature nanotechnology.
[16] D. Fang,et al. Silicane nanoribbons: electronic structure and electric field modulation , 2014 .
[17] K. Müllen. Evolution of graphene molecules: structural and functional complexity as driving forces behind nanoscience. , 2014, ACS nano.
[18] H. Sakaguchi,et al. Width‐Controlled Sub‐Nanometer Graphene Nanoribbon Films Synthesized by Radical‐Polymerized Chemical Vapor Deposition , 2014, Advanced materials.
[19] R. Sundaram,et al. Graphene nanoribbon blends with P3HT for organic electronics. , 2014, Nanoscale.
[20] Xinliang Feng. Synthesis of Structurally Well‐Defined and Liquid‐Phase‐Processable Graphene Nanoribbons. , 2014 .
[21] Juanxia Wu,et al. Raman spectroscopy of graphene , 2014 .
[22] A. Sinitskii,et al. Large-scale solution synthesis of narrow graphene nanoribbons , 2014, Nature Communications.
[23] K. Kim,et al. Charge-Transport Tuning of Solution-Processable Graphene Nanoribbons by Substitutional Nitrogen Doping , 2013 .
[24] F. Fischer,et al. Tuning the band gap of graphene nanoribbons synthesized from molecular precursors. , 2013, ACS nano.
[25] Zhirong Liu,et al. Inverse relationship between carrier mobility and bandgap in graphene. , 2013, The Journal of chemical physics.
[26] K. Schanze,et al. It takes more than an imine: the role of the central atom on the electron-accepting ability of benzotriazole and benzothiadiazole oligomers. , 2012, Journal of the American Chemical Society.
[27] G. Hilt,et al. Understanding the regioselectivity in Scholl reactions for the synthesis of oligoarenes. , 2012, Chemical communications.
[28] H. Bock,et al. Highly twisted arenes by Scholl cyclizations with unexpected regioselectivity. , 2011, Angewandte Chemie.
[29] Dustin K. James,et al. Graphene Chemistry: Synthesis and Manipulation , 2011 .
[30] L. Toppare,et al. Benzotriazole containing conjugated polymers for multipurpose organic electronic applications , 2011 .
[31] K. Müllen,et al. Graphene nanoribbons by chemists: nanometer-sized, soluble, and defect-free. , 2011, Angewandte Chemie.
[32] A. Seitsonen,et al. Atomically precise bottom-up fabrication of graphene nanoribbons , 2010, Nature.
[33] J. Maultzsch,et al. Symmetry properties of vibrational modes in graphene nanoribbons , 2010, 1003.0328.
[34] J. Tour,et al. Longitudinal unzipping of carbon nanotubes to form graphene nanoribbons , 2009, Nature.
[35] Edwin C. Kan,et al. Armchair graphene nanoribbons: Electronic structure and electric-field modulation , 2008, 0803.1233.
[36] Klaus Müllen,et al. Two-dimensional graphene nanoribbons. , 2008, Journal of the American Chemical Society.
[37] H. Dai,et al. Chemically Derived, Ultrasmooth Graphene Nanoribbon Semiconductors , 2008, Science.
[38] L. Novotný,et al. Optical Measurement of the Phase-Breaking Length in Graphene , 2008, 1008.1563.
[39] Jian Zhou,et al. Vibrational property and Raman spectrum of carbon nanoribbon , 2007 .
[40] M. Rooks,et al. Graphene nano-ribbon electronics , 2007, cond-mat/0701599.
[41] Hans-Joachim Egelhaaf,et al. Optical Bandgaps of π‐Conjugated Organic Materials at the Polymer Limit: Experiment and Theory , 2007 .
[42] S. Louie,et al. Energy gaps in graphene nanoribbons. , 2006, Physical review letters.
[43] Dmitri E. Nikonov,et al. Analysis of graphene nanoribbons as a channel material for field-effect transistors , 2006 .
[44] S. Konchenko,et al. Cyclic aryleneazachalcogens: Synthesis, vibrational spectra, and π-electron structures , 1990 .
[45] I. K. Korobeinicheva,et al. On the ``selenation'' method of assignment of organic sulphur compounds vibrational spectra , 1990 .
[46] M. Tommasini,et al. Helically Coiled Graphene Nanoribbons. , 2017, Angewandte Chemie.
[47] L. Novotný,et al. Low temperature raman study of the electron coherence length near graphene edges. , 2011, Nano letters.
[48] H. Dai,et al. Narrow graphene nanoribbons from carbon nanotubes , 2009, Nature.
[49] J. Bell,et al. Experiment and Theory , 1968 .