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Single molecule's conductance depending on its orientation
KTH, Skolan för bioteknologi (BIO), Teoretisk kemi (stängd 20110512).
KTH, Skolan för bioteknologi (BIO), Teoretisk kemi (stängd 20110512).
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2009 (Engelska)Ingår i: The Journal of Physical Chemistry C, ISSN 1932-7447, E-ISSN 1932-7455, Vol. 113, nr 1, s. 26-30Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Single molecules of 1,1,2,3,4,5-hexaphenylsilole adsorbed on Cu(111) have been investigated using low-temperature scanning tunneling microscopy, scanning tunneling spectroscopy, and quantum chemistry calculations. Two adsorption states have been identified, showing distinctive tunneling conductance. The molecules can switch their states under tip influence. Theoretical calculations indicate that the two states are associated with molecules adsorbed at two 90°-rotated orientations, and the tunneling conductance is attributed to molecular orbitals that spatially bridge tip-to-substrate gap. Our findings demonstrate a decisive dependence of single-molecule conductance on the molecular orientation with respect to electrodes.

Ort, förlag, år, upplaga, sidor
2009. Vol. 113, nr 1, s. 26-30
Nyckelord [en]
transport-properties, junction conductance, electron-transport, surface, atom, 2, 3, 4, 5-tetraphenylsiloles, conductivity, gold
Nationell ämneskategori
Kemi
Identifikatorer
URN: urn:nbn:se:kth:diva-33364DOI: 10.1021/jp8089215ISI: 000262168000006Scopus ID: 2-s2.0-65249167503OAI: oai:DiVA.org:kth-33364DiVA, id: diva2:414686
Tillgänglig från: 2011-05-04 Skapad: 2011-05-04 Senast uppdaterad: 2017-12-11Bibliografiskt granskad
Ingår i avhandling
1. Understanding the Structure and Reaction of Single Molecules on Metal surfaces from First Principles
Öppna denna publikation i ny flik eller fönster >>Understanding the Structure and Reaction of Single Molecules on Metal surfaces from First Principles
2011 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

The study of surface adsorption and reaction is not only interesting from a scientific point of view, but also important in many application fields such as energy, environment, catalysis, corrosion, electronic device, and sensor. Theoretical calculations are essential in these studies.

In this thesis, first principles studies for the structure and reaction of some important single molecules on the surface are presented. Dehydrogenation of single trans-2-butene molecule on a Pd(110) surface is the first example. The adsorption configurations of both reactant and produce are assigned and the whole dehydrogenation pathway is revealed. Our calculations show that the reactant, i.e. trans-2-butene molecule, undergoes a rotation before dehydrogenation occurs, which is an important detail that cannot be observed directly in scanning tunneling microscopy (STM) experiments. The dissociation and rotation processes of single oxygen molecule on a Pt(111) surface have been a subject of extensive studies in the past. A new intermediate state with a peculiar configuration is identified. The puzzled adsorption site is well explained. The calculated energy barriers agree well with experimental results for both dissociation and rotation processes.

Another aspect addressed in this thesis is the mechanism of molecular electronic switches induced by molecular structural changes. By carefully examining the tautomerization process of a naphthalocyanine molecule, an intermediate state is located on the potential surface of the tautomerization. Our calculations indicate that the experimentally observed switching involves four-states, rather than the two-state as proposed by the experimentalists. In a joint experimental and theoretical study the dehydrogenation, tautomerization, and mechanical switching processes of a single melamine molecule on a Cu(100) surface have been comprehensively examined. A new dual-functional molecular device with integrated rectifying and switching functions is made for the first time. In collaborating with another experimental group, we have simulated the switching process of a single 1,1,2,3,4,5-hexaphenylsilole molecule on a Cu(111) surface. The role of the orientation of the molecule is carefully examined and a new switching mechanism is proposed.

Switching processes are strongly associated with the inelastic electron tunneling. We have proposed a statistical model that allows explaining the non-integer exponent in the power-law relationship between the switching rate and tunneling current. In this model, the importance of the randomness in inelastic electron excitations and the lifetime of the immediate state are emphasized. It has shown that the inelastic electron tunneling is a collection of various n-electron processes with different statistical weight.

Ort, förlag, år, upplaga, sidor
Stockholm: KTH Royal Institute of Technology, 2011. s. xii, 72
Serie
Trita-BIO-Report, ISSN 1654-2312 ; 2011:16
Nationell ämneskategori
Teoretisk kemi
Identifikatorer
urn:nbn:se:kth:diva-33565 (URN)978-91-7415-978-3 (ISBN)
Disputation
2011-06-10, FA32, AlbaNova University Center, Roslagstullsbacken 21, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning
QC 20110524Tillgänglig från: 2011-05-24 Skapad: 2011-05-10 Senast uppdaterad: 2011-05-24Bibliografiskt granskad

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Yi, Luo

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Jun, JiangQiang, FuYi, Luo
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The Journal of Physical Chemistry C
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Totalt: 101 träffar
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