“…Based on electrospray ionisation [4], HV-ESD gives the possibility to study complex or fragile molecules that are impossible to safely deposit onto surfaces with traditional deposition techniques. So far, using HV-ESD, numerous molecular species with potential applications in biology and photovoltaics, or with magnetic or thermal expansion properties have been deposited on a variety of materials, ranging from metal surfaces [5][6][7][8][9][10][11][12][13], over metal oxides [14] and insulating substrates [15] to graphene monolayers on metals [16]. In HV-ESD-based devices, a solution containing the molecules reaches an emitter located in front of the entrance capillary, as shown in Figure 1a.…”
Maintaining clean conditions for samples during all steps of preparation and investigation is important for scanning probe studies at the atomic or molecular level. For large or fragile organic molecules, where sublimation cannot be used, high-vacuum electrospray deposition is a good alternative. However, because this method requires the introduction into vacuum of the molecules from solution, clean conditions are more difficult to be maintained. Additionally, because the presence of solvent on the surface cannot be fully eliminated, one has to take care of its possible influence. Here, we compare the high-vacuum electrospray deposition method to thermal evaporation for the preparation of C60 on different surfaces and compare, for sub-monolayer coverages, the influence of the deposition method on the formation of molecular assemblies. Whereas the island location is the main difference for metal surfaces, we observe for alkali halide and metal oxide substrates that the high-vacuum electrospray method can yield single isolated molecules accompanied by surface modifications.
“…Based on electrospray ionisation [4], HV-ESD gives the possibility to study complex or fragile molecules that are impossible to safely deposit onto surfaces with traditional deposition techniques. So far, using HV-ESD, numerous molecular species with potential applications in biology and photovoltaics, or with magnetic or thermal expansion properties have been deposited on a variety of materials, ranging from metal surfaces [5][6][7][8][9][10][11][12][13], over metal oxides [14] and insulating substrates [15] to graphene monolayers on metals [16]. In HV-ESD-based devices, a solution containing the molecules reaches an emitter located in front of the entrance capillary, as shown in Figure 1a.…”
Maintaining clean conditions for samples during all steps of preparation and investigation is important for scanning probe studies at the atomic or molecular level. For large or fragile organic molecules, where sublimation cannot be used, high-vacuum electrospray deposition is a good alternative. However, because this method requires the introduction into vacuum of the molecules from solution, clean conditions are more difficult to be maintained. Additionally, because the presence of solvent on the surface cannot be fully eliminated, one has to take care of its possible influence. Here, we compare the high-vacuum electrospray deposition method to thermal evaporation for the preparation of C60 on different surfaces and compare, for sub-monolayer coverages, the influence of the deposition method on the formation of molecular assemblies. Whereas the island location is the main difference for metal surfaces, we observe for alkali halide and metal oxide substrates that the high-vacuum electrospray method can yield single isolated molecules accompanied by surface modifications.
We present a thorough soft x-ray photoelectron spectroscopy (XPS) study of a mesoporous titanium dioxide electrode sensitized with the dye 4-(diphenylamino)phenylcyanoacrylic acid, referred to as “L0.” Supported by calculations, the suite of XPS, x-ray absorption spectroscopy, and resonant photoelectron spectroscopy allows us to examine bonding interactions between the dye and the surface and the frontier electronic structure at the molecule–oxide interface. While placing these measurements in the context of existing literature, this paper is intended as a useful reference for further studies of more complex triphenylamine based sensitizers.
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