Creazzo, FabrizioKetkaew, RangsimanSivula, KevinLuber, Sandra2022-09-122022-09-122022-09-122022-11-0110.1016/j.apsusc.2022.154203https://infoscience.epfl.ch/handle/20.500.14299/190633WOS:000848099600003An extensive understanding of WO3 and WSe2 bulk crystalline structures and explicit solvent effects on (001)-WO3 and (100)-WSe2 facets are essential for design of efficient (photo) electrocatalysts. The atomistic level understanding of both WO(3 )and WSe2 bulk solids and how water solvation processes occur on WO3 and WSe2 facets are nowadays characterized by a noticeable lack of knowledge. Herein, forefront Density Functional Theory-based molecular dynamics have been conducted for assessing the role of an explicit water environment in the characterization of solid surfaces. Water at the interface and H-bonds environment, as well as WO3 and WSe2 surface activity, will be described in terms of surface wettability and interfacial water dynamics, revealing the relevance of treating explicitly liquid water and its dynamics in assessing catalytic features. We provide pieces of evidence of the hydrophobic character shown by (001)-WO3 and (100)-WSe2 facets. A preferential in-plane hydration structure of the first water layer has been detected at both (001)-WO3 and (100)-WSe2 water interface, in which the electric dipole moment of water molecules is re-oriented in a sort of 2-dimensional H-bond network. Bulk property calculations of WO3 and WSe2 are also provided.Chemistry, PhysicalMaterials Science, Coatings & FilmsPhysics, AppliedPhysics, Condensed MatterChemistryMaterials SciencePhysicsdft-mdtungsten oxide wo3tungsten selenide wse2waterx-ray absorption spectroscopyx-ray-diffractionab-initioelectronic-structurehydrogen evolutiontungsten trioxideoptical-propertieswse2 nanosheetsband-gapwo3text::journal::journal article::research article