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Giacomo Giorgi

Publications and source records attributed to Giacomo Giorgi.

13 recordsLinked to original sources
arXiv2025

Suppressing metal molecule charge transfer with a phosphorus interlayer

Porphyrins are organic molecules that exhibit excellent opto-electronics properties, making them suitable for a variety of applications. Nevertheless, their functionality strongly depends on the surface onto which they are deposited, and on the interaction between the molecules and the substrate itself, which often leads to an undesired alteration in their electronic properties. In this study, we use a phosphorus interlayer on a Cu(110) surface as a buffer layer for the electronic decoupling of Zinc-TetraPhenylPorphyrin (ZnTPP) molecules. Using a combination of complementary techniques, such as Near Edge X-ray Absorption Fine Structure (NEXAFS), X-ray and Ultraviolet Photoemission Spectroscopy (XPS, UPS) as well as Scanning Tunneling Spectroscopy (STS) techniques, it is shown how the charge transfer from the metal, responsible for quenching the ZnTPP lowest unoccupied molecular level (LUMO) levels, is effectively prevented by the presence of a phosphorus reconstruction in between.

cond-mat.mes-hall↗
arXiv2025

A conformal approach to matter coupled Aristotelian gravity

We show how to take the first step in the conformal program for constructing general matter couplings to Aristotelian gravity with arbitrary $p$-brane foliation. For this purpose we extend the $p$-brane Aristotelian algebra to the direct sum of two conformal algebras: one with Minkowski signature for the longitudinal directions and a second one with Euclidean signature for the transverse directions. For some cases, it is sufficient to work with a subalgebra of this conformal extension that, instead of two dilatations that are isotropic in either the longitudinal or transverse directions, contains a single dilatation that acts on the longitudinal and transverse directions in an an-isotropic way. Using this conformal extension we show how different electric and magnetic versions of Aristotelian gravity can be constructed that all have the distinguishing property that they are not invariant under any (Galilean or Carrollian) boost symmetry. We next consider several matter couplings both for quadratic-derivative models as well as for some higher-derivative models that have recently been considered in connection with studies on fractons.

hep-th↗
arXiv2025

CO$_2$ adsorption and photocatalytic reduction mechanisms on Ti-terminated CaTiO$_3$ (100) surface: a DFT study

Photoreduction of CO$_2$ is an important alternative approach aimed to reduce the CO$_2$ atmospheric content which is responsible of the global warming. The development of an efficient photocatalyst can strongly improve the efficiency and selectivity of the by-products of such a process. Recently, CaTiO$_3$ has been used as an alternative semiconductor catalyst due to its attractive properties. In this study, we use calculations of the electronic structure of first principles to investigate for the first time the general reaction mechanism that leads to the main value-added by-products of HCOOH, CO, H$_3$COH and CH$_4$ byproducts, focusing on the reactions of adsorption, activation and reduction reactions of CO$_2$ molecules on the Ti-terminated CaTiO$_3$ (100) surface. We compute adsorption energies of the various intermediate configurations and activation energy barriers of the chemical reaction pathways. Our results show that CO$_2$ can be activated by charge transfer of excess electrons leading to a CO$_2$ anion that probably gives HCOO by the first reduction; however, the second hydrogenation to HCOOH is impeded by the prohibitive energy barrier. In particular, activated CO$_2$ can also easily undergo decomposition, which facilitates CO production. Afterwards, we discuss the possible reaction mechanisms of CO photoreduction towards H$_3$COH and CH$_4$ value-added products, taking into account the experimental evidence that only CO and CH$_4$ have been detected. The reaction pathway generally follows the most energetically convenient routes characterized by activated intermediates. Even though H$_3$COH could be finally produced, its strong adsorption ($E_{ads}$ of -0.93 eV) and its promoted decomposition to H$_3$CO+H on the surface could explain why it has not been detected, as opposed to CH$_4$ whose $E_{ads}$ is only -0.22 eV due to its non-polar nature.

cond-mat.mtrl-sci↗
arXiv2024

From Relativistic Gravity to the Poisson Equation

We consider the non-relativistic limit of general relativity coupled to a $(p+1)$-form gauge field and a scalar field in arbitrary dimensions and investigate under which conditions this gives rise to a Poisson equation for a Newton potential describing Newton-Cartan gravity outside a massive $p$-dimensional extended object, a so-called $p$-brane. Given our Ansatz, we show that not all the $p$-branes satisfy the required conditions. We study theories whose dynamics is defined by a Lagrangian as well as systems that are defined by a set of equations of motion not related to a Lagrangian. We show that, within the Lagrangian approach, a Poisson equation can be obtained provided that the coupling of the scalar field is fine-tuned such that the non-relativistic Lagrangian is invariant under an emerging local dilatation symmetry. On the other hand, we demonstrate that in the absence of a Lagrangian a Poisson equation can be obtained from a set of equations of motion that is not dilatation invariant. We discuss how our Ansatz could be generalized such as to include more $p$-branes giving rise to a Poisson equation.

hep-th↗
arXiv2024

On Non Invertible Symmetries in Type IIB Supergravity

In this work, we uncover a collection of non invertible topological operators linked to the 0-, 2-, 4- and 6-form symmetries related to the type IIB superstring effective theory. By pinpointing the $\text{SL}(2,\mathbb{Z})$-covariant conserved currents corresponding to these symmetries, we first derive a set of $\text{SL}(2,\mathbb{Z})$ invariant invertible topological operators that encapsulate the integer BPS charges inherent to the theory. Moving forward, by incorporating fractional charges while maintaining gauge invariance, we introduce the non invertible topological operators for each generalized symmetry, and in particular for the $\text{SL}(2,\mathbb{Z})$ 0-form symmetry. Identifying them as a novel kind of symmetries reminiscent of fractional quantum Hall effect (FQHE)-like non invertible operators, we study their action on charged objects and their associated SymTFTs obtained via half (higher) gauging.

hep-th↗
arXiv2024

Democratic actions with scalar fields: symmetric sigma models, supergravity actions and the effective theory of the type IIB superstring

The dualization of the scalar fields of a theory into (d-2)-form potentials preserving all the global symmetries is one of the main problems in the construction of democratic pseudoactions containing simultaneously all the original fields and their duals. We study this problem starting with the simplest cases and we show how it can be solved for scalars parametrizing Riemannian symmetric sigma-models as in maximal and half-maximal supergravities. Then, we use this result to write democratic pseudoactions for theories in which the scalars are non-minimally coupled to (p+1)-form potentials in any dimension. These results include a proposal of democratic pseudoaction for the generic bosonic sector of 4-dimensional maximal and half-maximal ungauged supergravities. Furthermore, we propose a democratic pseudoaction for the bosonic sector of N=2B,d=10 supergravity (the effective action of the type IIB superstring theory) containing two 0-, two 2-, one 4-, two 6- and three 8-forms which is manifestly invariant under global SL(2,R) transformations.

hep-th↗
arXiv2022

Exciton ground state fine structure and excited states landscape in layered halide perovskites from combined BSE simulations and symmetry analysis

Layered halide perovskites are solution-processed natural heterostructures where quantum and dielectric confinement effects down to the nanoscale strongly influence the optical properties, leading to stabilization of bound excitons. Achieving a detailed understanding of the exciton properties is crucial to boost the exploitation of these materials in energy conversion and light emission applications, with current on-going debate related to the energy order of the four components of the most stable exciton. To provide theoretical feedback and solve among contrasting literature reports, we perform here ab-initio solution of the Bethe Salpeter Equation (BSE), with detailed interpretation of the spectroscopic observables based on symmetry-analysis. We confirm the Edark < Ein plane < Eout-of-plane fine-structure assignment, as from recent magneto-absorption experiments. We further suggest that polar distortions may lead to stabilization of the in-plane component and ultimately end-up in a bright lowest exciton component. Also, we discuss the exciton landscape over a broad energy range and clarify the exciton spin-character, when large spin-orbit coupling is in play, to rationalize the potential of halide perovskites as triplet sensitizers in combination with organic dyes. In addition to contributing to the current understanding of the exciton properties of layered halide perovskites, the work further evidence the in-depth knowledge gained by combining advanced ab-initio simulations and group theory.

cond-mat.mtrl-sci↗
arXiv2018

Role of Quantum-Confinement in Anatase Nanosheets

Despite most of the applications of anatase nanostructures rely on photoexcited charge processes, yet profound theoretical understanding of fundamental related properties is lacking. Here, by means of ab initio ground and excited-state calculations, we reveal, in an unambiguous way, the role of quantum confinement effect and of the surface orientation, on the electronic and optical properties of anatase nanosheets (NSs). The presence of bound excitons extremely localized along the (001) direction, whose existence has been recently proven also in anatase bulk, explains the different optical behavior found for the two orientations (001) and (101) when the NS thickness increases. We suggest also that the almost two-dimensional nature of these excitons can be related to the improved photoconversion efficiency observed when a high percentage of (001) facet is present in anatase nanocrystals.

cond-mat.mtrl-sci↗
arXiv2016

A Novel Nanoporous Graphite Based on Graphynes: First Principles Structure and Carbon Dioxide Preferential Physisorption

Ubiquitous graphene is a stricly 2D material representing an ideal adsorbing platform due to its large specific surface area as well as its mechanical strength and resistance to both thermal and chemical stresses. However, graphene as a bulk material has the tendency to form irreversible agglomerates leading to 3D graphitic structures with a significant decrease of the area available for adsorption and no room for gas intercalation. In this paper a novel nanoporous graphite formed by graphtriyne sheets is introduced: its 3D structure is theoretically assessed by means of electronic structure and molecular dynamics computations within the DFT level of theory. It is found that the novel layered carbon allotrope is almost as compact as pristine graphite but the inherent porosity of the 2D graphyne sheets and its relative stacking leads to nanochannels that cross the material and whose sub-nanometer size could allow the diffusion and storage of gas species. A molecular prototype of the nanochannel is used to accurately determine first principles adsorption energies and enthalpies for CO2, N2, H2O and H2 within the pores. The proposed porous graphite presents no significant barrier for gas diffusion and it shows a high propensity for CO2 physisorption with respect to the other relevant components in both pre- and post-combustion gas streams.

cond-mat.mtrl-sci↗
arXiv2015

First Principles Investigation of Hydrogen Physical Adsorption on Graphynes' layers

Graphynes are 2D porous structures deriving from graphene featuring triangular and regularly distributed subnanometer pores, which may be exploited to host small gaseous species. First principles adsorption energies of molecular hydrogen (H2) on graphene, graphdiyne and graphtriyne molecular prototypes are obtained at the MP2C level of theory. First, a single layer is investigated and it is found that graphynes are more suited than graphene for H2 physical adsorption since they provide larger binding energies at equilibrium distances much closer to the 2D plane. In particular, for graphtriyne a flat minimum located right in the geometric center of the pore is identified. A novel graphite composed of graphtriyne stacked sheets is then proposed and an estimation of its 3D arrangement is obtained at the DFT level of theory. In contrast to pristine graphite this new carbon material allow both H2 intercalation and out-of-plane diffusion by exploiting the larger volume provided by its nanopores. Related H2 binding energies for intercalation and in-pore adsorption are around 0.1 eV and they could lead to high storage capacities. The proposed carbon-based layered material could represent a safer and potentially cheaper alternative for hydrogen on-board storage than conventional solutions based on cryogenic liquefaction and/or high compression.

physics.chem-ph↗
arXiv2014

Graphdiyne based membranes: exceptional performances for helium separation applications

Graphdiyne is a novel two-dimensional material deriving from graphene that has been recently synthesized and featuring uniformly distributed sub-nanometer pores. We report accurate calculations showing that graphdiyne pores permit an almost unimpeded helium transport which can be used for its chemical and isotopic separation. Exceptionally high He/CH_4 selectivities are found which largely exceed the performance of the best membranes used to date for extraction from natural gas. Moreover, by exploiting slight differences in the tunneling probabilities of ^3He and ^4He, we also find promising results for the separation of the Fermionic isotope at low temperature.

cond-mat.mes-hall↗
arXiv2014

The penetration barrier of water through graphynes' pores: first-principles predictions and force field optimization

Graphynes are novel two-dimensional carbon-based materials that -due to their nanoweb-like structure- have been proposed as molecular filters, especially for water purification technologies. In this work we carry out first principles electronic structure calculations at the MP2C level of theory to assess the interaction between water and graphyne, graphdiyne and graphtriyne pores. The computed penetration barriers suggest that water transport is unfeasible through graphyne while being unimpeded for graphtriyne. Nevertheless, for graphdiyne, which presents a pore size almost matching that of water, a low barrier is found which in turn disappears if an active hydrogen bond with an additional water molecule on the opposite side of the opening is taken into account. These results support the possibility of using graphtriyne as an efficient membrane for water filtration but, in contrast with previous determinations, they do not exclude graphdiyne. In fact, the related first principles penetration barrier leads to water permeation probabilities which are at least two order of magnitude larger than those estimated by employing commonly used force fields. A new pair potential for the water--carbon non-covalent component of the interaction has been built and it is recommended for molecular dynamics simulation involving graphdiyne and water.

physics.chem-ph↗