International audienceUsing an ab initio electrochemical approach, we show that the water monolayer on Pd(111) undergoes a first order transition as the surface charge is tuned, with a phase equilibrium between two modified ice structures on opposite charged substrates. These findings refine the classical H-down and H-up configurations by invoking a permanent charged surface. We explore the experimental consequences of this phase behaviour on scanning tunneling microscopy (STM) with STM simulations. A strong dependence of the topographic contrast with surface charge (or equivalently STM potential) is exhibited allowing to reinterprete recent experimental observations
The structure and properties of water films in contact with metal surfaces are crucial to understand...
The comprehension of the mechanisms underlying the charge distribution at the electrochemical interf...
The interface between an electrode and an electrolyte is where electrochemical processes take place ...
International audienceWe present a theoretical study of the structural response of model water monol...
The mass and charge distribution at electrochemical interfaces plays a key role in driving electroch...
Interactions between molecules and electrode surfaces play a key role in electrochemical processes a...
Adenine and 2-2\u27 bipyridine monolayer films adsorbed on Au (111) have been studied by Scanning Tu...
Atomically flat, single-crystal solid-liquid interfaces attract considerable interest through their ...
Crystal surfaces which generate polar repeat units are fundamentally unstable on electrostatic groun...
An extensive amount of literature can be found containing experimental and theoretical studies of wa...
We perform atomistic simulations of nanometer-separated charged surfaces in the presence of monovale...
Potential-induced structural change in a self-assembled monolayer (SAM) of 4-methylbenzenethiol (4-M...
We present a detailed voltage-dependent scanning tunneling microscopy study of a single phosphorus a...
The results of molecular dynamics simulations of the properties of water in an aqueous ionic solutio...
The structure and properties of water films in contact with metal surfaces are crucial to understand...
The structure and properties of water films in contact with metal surfaces are crucial to understand...
The comprehension of the mechanisms underlying the charge distribution at the electrochemical interf...
The interface between an electrode and an electrolyte is where electrochemical processes take place ...
International audienceWe present a theoretical study of the structural response of model water monol...
The mass and charge distribution at electrochemical interfaces plays a key role in driving electroch...
Interactions between molecules and electrode surfaces play a key role in electrochemical processes a...
Adenine and 2-2\u27 bipyridine monolayer films adsorbed on Au (111) have been studied by Scanning Tu...
Atomically flat, single-crystal solid-liquid interfaces attract considerable interest through their ...
Crystal surfaces which generate polar repeat units are fundamentally unstable on electrostatic groun...
An extensive amount of literature can be found containing experimental and theoretical studies of wa...
We perform atomistic simulations of nanometer-separated charged surfaces in the presence of monovale...
Potential-induced structural change in a self-assembled monolayer (SAM) of 4-methylbenzenethiol (4-M...
We present a detailed voltage-dependent scanning tunneling microscopy study of a single phosphorus a...
The results of molecular dynamics simulations of the properties of water in an aqueous ionic solutio...
The structure and properties of water films in contact with metal surfaces are crucial to understand...
The structure and properties of water films in contact with metal surfaces are crucial to understand...
The comprehension of the mechanisms underlying the charge distribution at the electrochemical interf...
The interface between an electrode and an electrolyte is where electrochemical processes take place ...