Alkali-Metal-Intercalated Percolation Network Regulates Self-Assembled Electronic Aromatic Molecules

被引:11
|
作者
Hu, Yong [1 ]
Zhong, Guohua [2 ]
Guan, Ying-Shi [1 ]
Lee, Nam Hoon [1 ]
Zhang, Yuan [3 ]
Li, Yang [3 ]
Mitchell, Travis [4 ]
Armstrong, Jason N. [1 ]
Benedict, Jason [4 ]
Hla, Saw-Wai [3 ]
Ren, Shenqiang [1 ]
机构
[1] Univ Buffalo State Univ New York, Res & Educ Energy Environm & Water RENEW Inst, Dept Mech & Aerosp Engn, Buffalo, NY 14260 USA
[2] Chinese Acad Sci, Shenzhen Inst Adv Technol, Shenzhen 518055, Peoples R China
[3] Argonne Natl Lab, Nanosci & Technol Div, Ctr Nanoscale Mat, Lemont, IL 60439 USA
[4] Univ Buffalo State Univ New York, Dept Chem, Buffalo, NY 14260 USA
基金
美国国家科学基金会;
关键词
aromatic molecule; charge-transfer; molecular self-assembly; percolation network; P-TERPHENYL; RAMAN CHARACTERIZATION; ORGANIC CONDUCTORS; X-RAY; BIPOLARONS; POLARONS; SUPERCONDUCTIVITY; TRANSITION; SOLITONS; STATE;
D O I
10.1002/adma.201807178
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the continuously growing field of correlated electronic molecular crystals, there is significant interest in addressing alkali-metal-intercalated aromatic hydrocarbons, in which the possibility of high-temperature superconductivity emerges. However, searching for superconducting aromatic molecular crystals remains elusive due to their small shielding fraction volume. To exploit this potential, a design principle for percolation networks of technologically important film geometry is indispensable. Here the effect of potassium-intercalation is shown on the percolation network in self-assembled aromatic molecular crystals. It is demonstrated that one-dimensional (1D) dipole pairs, induced by dipole interaction, regulate the conductivity, as well as the electronic and optical transitions, in alkalimetal-intercalated molecular electronic crystals. A solid-solution growth methodology of aromatic molecular films with a broad range of stability is developed to uncover electronic and optical transitions of technological importance. The light-induced electron interactions enhance the charge-carrier itinerancy, leading to a switchable metal-to-insulator transition. This discovery opens a route for the development of aromatic molecular electronic solids and long-term modulation of electronic efficacy in nano-technologically important thin films.
引用
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页数:9
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