Counterintuitive issues in the charge transport through molecular junctions
Literature Information
Ioan Bâldea
Whether at phenomenological or microscopic levels, most theoretical approaches to charge transport through molecular junctions postulate or attempt to justify microscopically the existence of a dominant molecular orbital (MO). Within such single level descriptions, experimental current–voltage I–V curves are sometimes/often analyzed by using analytical formulas expressing the current as a cubic expansion in terms of the applied voltage V, and the possible V-driven shifts of the level energy offset relative to the metallic Fermi energy ε0 are related to the asymmetry of molecule–electrode couplings or an asymmetric location of the “center of gravity” of the MO with respect to electrodes. In this paper, we present results demonstrating the failure of these intuitive expectations. For example, we show how typical data processing based on cubic expansions yields a value of ε0 underestimated by a typical factor of about two. When compared to theoretical results of DFT approaches, which typically underestimate the HOMO–LUMO gap by a similar factor, this may create the false impression of “agreement” with experiments in situations where this is actually not the case. Furthermore, such cubic expansions yield model parameter values dependent on the bias range width employed for fitting, which is unacceptable physically. Finally, we present an example demonstrating that, counter-intuitively, the bias-induced change in the energy of an MO located much closer to an electrode can occur in a direction that is opposite to the change in the Fermi energy of that electrode. This is contrary to what one expects based on a “lever rule” argument, according to which the MO “feels” the local value of the electric potential, which is assumed to vary linearly across the junction and is closer to the potential of the closer electrode. This example emphasizes the fact that screening effects in molecular junctions can have a subtle character, contradicting common intuition.
Related Literature
UV induced local heating effects in TiO2nanocrystals
Thomas Berger, Oliver Diwald, Erich Knözinger, Martin Sterrer, John T. Yates Jr
DOI: 10.1039/B517107E
Urethane cross-linked poly(oxyethylene)/siliceous nanohybrids doped with Eu3+ ions Part 2. Ionic association
Verónica de Zea Bermudez, Denis Ostrovskii, Sergei Lavoryk, M. Cristina Gonçalves, Luís D. Carlos
DOI: 10.1039/B308202D
A comparison of water adsorption on ordered and disordered silica substrates
Joël Puibasset, Roland J.-M. Pellenq
DOI: 10.1039/B313001K
The role of FA:K+ and FA:Na+ defects in laser light generation and color image formation at the (100) and (110) surface sites of AgCl and AgBr. First principles calculations
A. S. Shalabi, I. A. Z. Al-Ansari, K. Kh. Al-Naimi, M. A. Kamel, A. M. El-Mahdy, H. O. Taha, M. M. Shalaby
DOI: 10.1039/B311839H
Investigation of interparticle interactions of larger (4.63 nm) monolayer protected gold clusters during quantized double layer charging
Nirmalya Kumar Chaki, Bhalchandra Kakade, Kunjukrishna Pillai Vijayamohanan, Poonam Singh, C. V. Dharmadhikari
DOI: 10.1039/B516650K
Modeling fluid diffusion using the lattice density functional theory approach: counterdiffusion in an external field
Daniel Matuszak, Gregory L. Aranovich, Marc D. Donohue
DOI: 10.1039/B516036G
Dynamic mobility of concentrated suspensions. Comparison between different calculations
F. J. Arroyo, F. Carrique, S. Ahualli, A. V. Delgado
DOI: 10.1039/B312839C
Heterogeneous reaction of ozone with hydrocarbon flame soot
Stéphane Lelièvre, Yuri Bedjanian, Nicolas Pouvesle, Jean-Louis Delfau, Christian Vovelle, Georges Le Bras
DOI: 10.1039/B316895F
You might also like
Is 6-(3-Fluorophenyl)picolinic acid (CAS: 887982-40-3) safe?
6-(3-Fluorophenyl)picolinic acid is generally considered safe for laboratory use...
What industries use (3R)-3-Pyrrolidinol (CAS: 2799-21-5)?
(3R)-3-Pyrrolidinol is used in the pharmaceutical industry as a precursor for dr...
What precautions should be taken when handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-8)?
When handling (4R,5R)-4,5-Diethoxycarbonyl-2,2-dimethyldioxolane (CAS: 59779-75-...
How is 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone (CAS: 90734-71-7) typically synthesized?
1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone is often synthesized via a mult...
What is the market or research trend for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1)?
The market for N-Ethyl-3,4-dimethylbenzylamine (CAS: 39180-83-1) remains steady,...
What is Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate (CAS: 1019008-21-9)?
Tert-butyl 3-(pyrrolidin-1-yl)azetidine-1-carboxylate is a chemical compound wit...
What regulatory guidelines apply to 1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1)?
1-Bromo-3-chloro-2,4-dimethoxybenzene (CAS: 1228956-93-1) falls under the classi...
Is 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07-4) safe?
The safety of 8-Bromo-2-methyl-3,4-dihydroisoquinolin-1(2H)-one (CAS: 1368622-07...
Is Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate (CAS: 22785-43-9) safe?
Benzyl [(3S)-2,6-dioxo-3-piperidinyl]carbamate is generally safe when handled wi...
How should 1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine (CAS: 928657-21-0) be stored?
1-{[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]sulfonyl}pyrrolidine s...
Source Journal
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.










![2-Methyl-2-propanyl [(2S)-1-hydroxy-3-(4-hydroxyphenyl)-2-propanyl]carbamate structure 2-Methyl-2-propanyl [(2S)-1-hydroxy-3-(4-hydroxyphenyl)-2-propanyl]carbamate structure](https://static.chemtradehub.com/structs/833/83345-46-4-eec2.webp)

![2-[({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)methyl]isonicotinic acid structure 2-[({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)methyl]isonicotinic acid structure](https://static.chemtradehub.com/structs/473/473924-63-9-973b.webp)

