Zigzag sp2 Carbon Chains Passing through an sp3 Framework: A Driving Force toward Room-Temperature Ferromagnetic Graphene

被引:19
作者
Tucek, Jiri [1 ]
Hola, Katrina [1 ]
Zoppellaro, Giorgio [1 ]
Blonski, Piotr [1 ]
Langer, Rostislav [1 ]
Medved', Miroslav [1 ]
Susi, Toma [2 ]
Otyepka, Michal [1 ]
Zboril, Radek [1 ]
机构
[1] Palacky Univ Olomouc, Fac Sci, Dept Phys Chem, Reg Ctr Adv Technol & Mat, Slechtitelu 27, Olomouc 78371, Czech Republic
[2] Univ Vienna, Fac Phys, Boltzmanngasse 5, A-1090 Vienna, Austria
基金
奥地利科学基金会; 欧洲研究理事会; 欧盟地平线“2020”;
关键词
hydroxofluorographene; fluorographene; magnetic carbon; hydroxyl; DFT calculations; density of states; 2D magnets; spintronics; ELECTRON-SPIN-RESONANCE; BIRCH REDUCTION; BASIS-SETS; MAGNETISM; CHEMISTRY; GRAPHITE; DERIVATIVES; FAMILY; FUNCTIONALIZATION; FLUOROGRAPHENE;
D O I
10.1021/acsnano.8b08052
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Stabilization of ferromagnetic ordering in graphene-based systems up to room temperature remains an important challenge owing to the huge scope for applications in electronics, spintronics, biomedicine, and separation technologies. To date, several strategies have been proposed, including edge engineering, introduction of defects and dopants, and covalent functionalization. However, these techniques are usually hampered by limited temperature sustainability of ferromagnetic ordering. Here, we describe a method for the well-controlled spa functionalization of graphene to synthesize zigzag conjugated sp(2) carbon chains that can act as communication pathways among radical motifs. Zigzag sp(2)/sp(3) patterns in the basal plane were clearly observed by high-resolution scanning transmission electron microscopy and provided a suitable matrix for stabilization of ferromagnetic ordering up due to combined contributions of itinerant pi-electrons and superexchange interactions. The results highlight the principal role of sp(2)/sp(3) ratio and superorganization of radical motifs in graphene for generating room-temperature nonmetallic magnets. to room temperature
引用
收藏
页码:12847 / 12859
页数:13
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