Nanopatterning Graphite Surface by Diazoniums Using Electrochemical Method

2021 ◽  
Vol 11 (1) ◽  
pp. 44-48
Author(s):  
Hai Phan Thanh ◽  
Hieu Vo Minh ◽  
Dien Nguyen Duy ◽  
Tinh Hoang Van ◽  
Trung Huynh Thi Mien

Molecular functionalization of graphitic surfaces with nanopatterned structures is regarded as one of the effective bottom-up techniques to tune their electronic properties towards electronics applications. Diazonium molecules have been often employed to covalently functionalize graphene and highly oriented pyrolytic graphite (HOPG) substrates. However, controlling the structure of the molecular adlayers is still challenging. In this contribution, we demonstrated an inconventional approach for covalent functionalization the HOPG surface by using mixture of 4-nitrobenzenediazonium (4-NBD) and 3,5-bis-tert-butylbenzenediazonium (3,5-TBD) molecules in which the former tends to polimezise and physisorb while the later chemically anchors on surface. The physisorbed features can be removed by washing with hot toluene and water. As a result, the HOPG surface is patterned in a quasi-periodic fashion. The efficiency of this development was verified by a combination of cyclic voltametry (CV) and atomic force microscopy (AFM) methods. This finding represents a convenient strategy for creating nanoconfined templates that might serve as nano-playgrounds for further supramolecular self-assembly and other on-surface reactions.




Scanning ◽  
2015 ◽  
Vol 37 (2) ◽  
pp. 158-164 ◽  
Author(s):  
XIAO Peng ◽  
HAORAN Fu ◽  
Ruisi Liu ◽  
Lin Zhao ◽  
Yuangang Zu ◽  
...  


Nanoscale ◽  
2017 ◽  
Vol 9 (36) ◽  
pp. 13707-13716 ◽  
Author(s):  
Anna D. Protopopova ◽  
Rustem I. Litvinov ◽  
Dennis K. Galanakis ◽  
Chandrasekaran Nagaswami ◽  
Nikolay A. Barinov ◽  
...  

High-resolution atomic force microscopy imaging reveals the role of fibrinogen αC regions in the early stages of fibrin self-assembly.



1997 ◽  
Vol 12 (8) ◽  
pp. 1942-1945 ◽  
Author(s):  
H. J. Gao ◽  
H. X. Zhang ◽  
Z. Q. Xue ◽  
S. J. Pang

Scanning tunneling microscopy (STM) and atomic force microscopy (AFM) investigation of tetracyanoquinodimethane (TCNQ) and the related C60-TCNQ thin films is presented. Periodic molecular chains of the TCNQ on highly oriented pyrolytic graphite (HOPG) substrates were imaged, which demonstrated that the crystalline (001) plane was parallel to the substrate. For the C60-TCNQ thin films, we found that there were grains on the film surface. STM images within the grain revealed that the well-ordered rows and terraces, and the parallel rows in different grains were generally not in the same orientation. Moreover, the grain boundary was also observed. In addition, AFM was employed to modify the organic TCNQ film surface for the application of this type of materials to information recording and storage at the nanometer scale. The nanometer holes were successfully created on the TCNQ thin film by the AFM.







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