Publications by authors named "Cesar D Mendoza"

Article Synopsis
  • * Density functional theory (DFT) calculations indicate negative binding energies for these metal ions on the heterostructures, confirmed by Surface Plasmon Resonance (SPR) spectroscopy, which measures strong binding in water according to a Langmuir isotherm model.
  • * Among the metal ions tested, mercury (Hg) displays the highest affinity and sensitivity, with impressive detection limits, and results suggest that electron transfer plays a crucial role in enhancing the performance of SPR sensors in detecting heavy metal ions.
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Understanding the interfacial electronic structures of organic semiconductor phthalocyanines (MePc) and graphene is essential for their practical application in various fields. In this study, we investigated the electronic structure and the tuning of the work function of free metal phthalocyanine (Pc4), cobalt phthalocyanine (CoPc), and copper phthalocyanine (CuPc) molecules deposited on a graphene monolayer using X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS). We found that the functionalization of MePc molecules induces p-doping to the graphene substrate due to the charge transfer mechanism with the MePc molecule.

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We investigated the interfacial electronic structure of the bidimensional interface of single-layer graphene on a germanium substrate. The procedure followed a well-established approach using ultraviolet (UPS) and X-ray (XPS) photoelectron spectroscopy. The direct synthesis of the single-layer graphene on the surface of (110) undoped Ge substrates was conducted via chemical vapor deposition (CVD).

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Organic/inorganic van der Waals heterojunctions formed by a combination of 2D materials with semiconductor polymer films enable the fabrication of new device architectures that are interesting for electronic and optoelectronic applications. Here, we investigated the charge-transfer dynamics at the interface between 2D layered franckeite (Fr) and two thiophene-based conjugated polymers (PFO-DBT and P3HT) from the resonantly core-excited electron. The unoccupied electronic states of PFO-DBT/Fr and P3HT/Fr heterojunctions were studied using near-edge X-ray absorption fine structure (NEXAFS) and resonant Auger (RAS) synchrotron-based spectroscopies.

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Hybrid van der Waals heterojunctions based on organic polymers and 2D materials have emerged as a promising solution for developing more efficient optoelectronic devices. Herein, we investigated the charge transfer (CT) dynamics at the interface of the poly[3-hexylthiophene-2,5-diyl] (P3HT) organic polymer and a MoS monolayer. A global picture of the charge transfer dynamics of a P3HT/MoS/SiO heterojunction was elucidated from photoluminescence (PL) spectroscopy and the fluorescence lifetime decay profile.

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Graphene grown directly on germanium is a possible route for the integration of graphene into nanoelectronic devices as well as it is of great interest for materials science. The morphology of the interface between graphene and germanium influences the electronic properties and has not already been completely elucidated at atomic scale. In this work, we investigated the morphology of the single-layer graphene grown on Ge substrates with different crystallographic orientations.

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