Recently, we investigated the adsorption of octachloro zinc phthalocyanine (ZnPcCl(8)) on Ag(111) by scanning tunneling microscopy. Compared to the standard phthalocyanine, halogenated phthalocyanine molecules show a much more complex binding behavior, which results in the formation of three different structural phases. These phases follow from the ordering process with the formation of 8, 4 and 0 intermolecular hydrogen-halogen bonds (Abel et al 2006 ChemPhysChem 7 82). In the present work we investigate these phases by Kelvin probe force microscopy in order to quantitatively deduce the electric interface barrier of the first monolayer. Our measurements reveal that the binding behavior does not only affect the structural ordering but also the interface dipole formation, which leads to different work functions. The fact that we observe interface barriers of opposite signs between ordered and disordered molecular layers underlines the importance of exactly knowing the molecular arrangement at the interface when assembling organic molecule devices.

Download full-text PDF

Source
http://dx.doi.org/10.1088/0957-4484/19/30/305501DOI Listing

Publication Analysis

Top Keywords

interface dipole
8
dipole formation
8
kelvin probe
8
probe force
8
force microscopy
8
binding behavior
8
interface
5
formation
4
formation znpccl8
4
phases
4

Similar Publications

Structural Basis of Ultralow Capacitances at Metal-Nonaqueous Solution Interfaces.

J Am Chem Soc

January 2025

State Key Laboratory of Materials-Oriented Chemical Engineering, College of Chemical Engineering, Nanjing Tech University, Nanjing 211816, China.

Metal-nonaqueous solution interfaces, a key to many electrochemical technologies, including lithium metal batteries, are much less understood than their aqueous counterparts. Herein, on several metal-nonaqueous solution interfaces, we observe capacitances that are 2 orders of magnitude lower than the usual double-layer capacitance. Combining electrochemical impedance spectroscopy, atomic force microscopy, and physical modeling, we ascribe the ultralow capacitance to an interfacial layer of 10-100 nm above the metal surface.

View Article and Find Full Text PDF

Asymmetric electronic distribution induced enhancement in photocatalytic CO-to-CH conversion via boron-doped covalent triazine frameworks.

J Colloid Interface Sci

January 2025

Department of Environmental Science and Engineering, Fuzhou University, Minhou, Fujian 350108, China; State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Minhou, Fujian 350108, China. Electronic address:

Covalent triazine frameworks (CTFs) are emerging as promising platform for photocatalysis, yet their highly symmetric structure leads to significant charge recombination. Herein, we employed a facile non-metallic boron (B) modification with precisely controlled doping site to introduce asymmetric local electron distribution in CTFs, achieving a 15-fold activity enhancement for CO-to-CH conversion. Calculations including frontier orbitals, dipole moments and molecular electrostatic potentials firmly demonstrated the formation of localized polarized electron regions in CTF-1 via B doping.

View Article and Find Full Text PDF

A cross-domain-based channel selection method for motor imagery.

Med Biol Eng Comput

January 2025

State Key Laboratory of Power Transmission Equipment Technology, School of Electrical Engineering, Chongqing, University, Chongqing, 400044, People's Republic of China.

Selecting channels for motor imagery (MI)-based brain-computer interface (BCI) systems can not only enhance the portability of the systems, but also improve the decoding performance. Hence, we propose a cross-domain-based channel selection (CDCS) approach, which effectively minimizes the number of EEG channels used while maintaining high accuracy in MI recognition. The EEG source imaging (ESI) technique is employed to map scalp EEG into the cortical source domain.

View Article and Find Full Text PDF

Enhancing ionic conductivity and expanding the electrochemical window in polymer electrolytes via ferroelectric-metal-organic-frameworks to manipulate charge spatial distribution.

J Colloid Interface Sci

January 2025

National Local Joint Engineering Research Center for Lithium-ion Batteries and Materials Preparation Technology, Key Laboratory of Advanced Batteries Materials of Yunnan Province, Faculty of Metallurgical and Energy Engineering, Kunming University of Science and Technology, Kunming 650093 China. Electronic address:

Poly (ethylene oxide) (PEO)-based polymer electrolytes have promising applications in all-solid-state lithium metal batteries. However, their wide range of practical applications is severely limited by their relatively low room temperature lithium ion conductivity and narrow electrochemical window. In this paper, based on the ability of spontaneous polarization of ferroelectric materials to generate polarization field under applied electric field and the characteristics of Metal-Organic-Frameworks (MOFs) materials with regular adjustable pore structure, a Nano material combining ferroelectric materials and MOF (NUS-6(Hf)-MOF) was first proposed to be added to PEO polymer electrolyte as a filler.

View Article and Find Full Text PDF

The effective collection of interfacial tribo-charges and an increase in load voltage are two essential factors that improve the output energy of triboelectric nanogenerators. However, some tribo-charges are hardly collected through one or multiple integrated side electrodes based on corona discharge, and their load voltages are limited by air breakdown in adjacent electrodes. In this study, a dynamic quasi-dipole potential distribution model is proposed to systematically reveal the mechanisms of interfacial tribo-charge loss.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!