Molecular vs. inorganic spintronics: the role of molecular materials and single molecules

2009 ◽  
Vol 19 (12) ◽  
pp. 1678 ◽  
Author(s):  
Julio Camarero ◽  
Eugenio Coronado
2004 ◽  
Vol 37 (16) ◽  
pp. 6132-6140 ◽  
Author(s):  
Pradeep Kumar ◽  
Adosh Mehta ◽  
Shannon M. Mahurin ◽  
Sheng Dai ◽  
Mark D. Dadmun ◽  
...  

2009 ◽  
Vol 9 (2) ◽  
pp. 982-990 ◽  
Author(s):  
Theresa Bullard ◽  
Kristin L. Wustholz ◽  
Eric D. Bott ◽  
Miranda Robertson ◽  
Philip J. Reid ◽  
...  

2015 ◽  
Vol 44 (4) ◽  
pp. 920-942 ◽  
Author(s):  
Edmund Leary ◽  
Andrea La Rosa ◽  
M. Teresa González ◽  
Gabino Rubio-Bollinger ◽  
Nicolás Agraït ◽  
...  

Constructing electronic circuits containing singly wired molecules is at the frontier of electrical device miniaturisation. Understanding the behaviour of different anchoring groups is key to this goal because of their significant role in determining the properties of the junction.


2016 ◽  
Vol 94 (19) ◽  
Author(s):  
T. K. Yamada ◽  
Y. Yamagishi ◽  
S. Nakashima ◽  
Y. Kitaoka ◽  
K. Nakamura
Keyword(s):  

2011 ◽  
Vol 40 (41) ◽  
pp. 10843 ◽  
Author(s):  
R. A. Allão ◽  
A. K. Jordão ◽  
J. A. L. C. Resende ◽  
A. C. Cunha ◽  
V. F. Ferreira ◽  
...  

2016 ◽  
Vol 88 (10-11) ◽  
pp. 1063-1071 ◽  
Author(s):  
Jacek Waluk

AbstractResults of thorough investigations of tautomerism in the ground and excited electronic states performed for various organic molecules under different regimes: condensed phases, isolated and single molecules, with a special emphasis on porphycene, a porphyrin isomer, demonstrate that, in order to precisely describe the proton/hydrogen transfer path, one has to explicitly consider tunneling. Tautomerization is a multidimensional process, controlled by excitation of specific vibrational modes. Vibrational excitation can both enhance or hinder the reaction. The role of specific vibrational modes can now be assessed, even at the level of single molecules.


2021 ◽  
Vol 11 (15) ◽  
pp. 6937
Author(s):  
Hidemasa Yamane ◽  
Nobuhiko Yokoshi ◽  
Hajime Ishihara

Near-field interactions between metallic surfaces and single molecules play an essential role in the application of metamaterials. To reveal the near-field around a photo-irradiated single molecule on the metallic surface, high-resolution photo-assisted scanning microscopy is required. In this study, we theoretically propose photoinduced force microscopy (PiFM) measurements of single molecules at the atomic resolution. For experimental demonstration, we performed a numerical calculation of PiFM images of various transition states, including optical forbidden transitions, and interpreted them in terms of the interaction between the molecular internal polarization structures and localized plasmon. We also clarified the critical role of atomic-scale structures on the tip surface for high-resolution PiFM measurements.


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