Wafer-scale synthesis of monolayer two-dimensional porphyrin polymers for hybrid superlattices

被引:211
|
作者
Zhong, Yu [1 ]
Cheng, Baorui [1 ]
Park, Chibeom [1 ,2 ]
Ray, Ariana [3 ]
Brown, Sarah [1 ,2 ]
Mujid, Fauzia [1 ]
Lee, Jae-Ung [4 ,5 ]
Zhou, Hua [6 ]
Suh, Joonki [1 ]
Lee, Kan-Heng [4 ,7 ]
Mannix, Andrew J. [2 ]
Kang, Kibum [1 ,2 ,8 ]
Sibener, S. J. [1 ,2 ]
Muller, David A. [7 ]
Park, Jiwoong [1 ,2 ,4 ]
机构
[1] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
[2] Univ Chicago, James Franck Inst, 5640 S Ellis Ave, Chicago, IL 60637 USA
[3] Cornell Univ, Dept Phys, Ithaca, NY 14853 USA
[4] Univ Chicago, Pritzker Sch Mol Engn, Chicago, IL 60637 USA
[5] Ajou Univ, Dept Phys, Suwon 16499, South Korea
[6] Argonne Natl Lab, Adv Photon Source, Lemont, IL 60439 USA
[7] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
[8] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Daejeon 34141, South Korea
基金
美国国家科学基金会;
关键词
ELECTRONIC-STRUCTURE; CHEMISTRY; POLYMERIZATION; SHEETS;
D O I
10.1126/science.aax9385
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The large-scale synthesis of high-quality thin films with extensive tunability derived from molecular building blocks will advance the development of artificial solids with designed functionalities. We report the synthesis of two-dimensional (2D) porphyrin polymer films with wafer-scale homogeneity in the ultimate limit of monolayer thickness by growing films at a sharp pentane/water interface, which allows the fabrication of their hybrid superlattices. Laminar assembly polymerization of porphyrin monomers could form monolayers of metal-organic frameworks with Cu2+ linkers or covalent organic frameworks with terephthalaldehyde linkers. Both the lattice structures and optical properties of these 2D films were directly controlled by the molecular monomers and polymerization chemistries. The 2D polymers were used to fabricate arrays of hybrid superlattices with molybdenum disulfide that could be used in electrical capacitors.
引用
收藏
页码:1379 / +
页数:42
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