Alessia Provino
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Alessia Provino has a total of 1000 co-authors. Here are the top co-authors by number of shared publications:
P. Manfrinetti
Department of Chemistry, University of Genova, Via Dodecaneso 31, 16146, Genova, Italy
32 shared publications- Pietro Manfrinetti
Consiglio Nazionale delle Ricerche
22 shared publications Pietro Manfrinetti
Univ Genoa, Dept Chem, Genoa, Italy
12 shared publications- Volodymyr Smetana
Department of Materials and Environmental Chemistry, Stockholm University, Svante Arrhenius väg 16c, 10691 Stockholm, Sweden
11 shared publications A.V. Morozkin
Department of Chemistry, Moscow State University, Leninskie Gory, House 1, Building 3, GSP-2, Moscow 119992, Russia
9 shared publicationsSudesh K. Dhar
8 shared publications
Latest Publications
- Open Access
- 18 August 2026
- Published by Elsevier in Acta Materialia
- Vol. 320
UNi4Mn: A non-centrosymmetric uranium intermetallic exhibiting room-temperature ferromagnetism
- 18 August 2026
- Published by Elsevier in Acta Materialia
- Vol. 320
Open AccessUNi4Mn: A non-centrosymmetric uranium intermetallic exhibiting room-temperature ferromagnetism
- Open Access
- 21 July 2026
- Published by Springer Nature in The European Physical Journal C
- Vol. 86 (7)
Erratum to: Future Circular Collider Feasibility Study Report
- 21 July 2026
- Published by Springer Nature in The European Physical Journal C
- Vol. 86 (7)
Open AccessErratum to: Future Circular Collider Feasibility Study Report
- Open Access
Phase Stability and Competing Crystal Structures in the Formation of the Intermetallic Compounds Cu5As2 and Cu5(As,Sb)2
An experimental investigation of the Cu-As-Sb ternary system in the Cu-rich region led to the identification of a new intermetallic phase, Cu5(As,Sb)2. The compound crystallizes in the orthorhombic Mg5Ga2-type structure (oI28, Ibam), analogous to the binary parent phase Cu5As2, with lattice parameters a = 5.968–5.977(1) Å, b = 11.550–11.565(3) Å, c = 5.530–5.573(3) Å. Similar to the parent Cu5As2 phase, the ternary compound forms with slight Cu under stoichiometry and exhibits a limited compositional range, with no continuous solid solubility between the binary and ternary phases. The phase formation, compositional stability, and decomposition behavior were systematically studied using a combination of powder and single-crystal X-ray diffraction (XRD, including Rietveld refinement), metallographic analysis with optical and scanning electron microscopy with energy-dispersive X-ray spectroscopy (LOM, SEM-EDXS), electron backscatter diffraction (EBSD) and thermal analysis (DTA, DSC). The results reveal that Cu5(As,Sb)2 is a high-temperature phase forming peritectically at 650–635 °C and stable only within a limited temperature interval. No continuous solid solubility exists between the ternary compound and the parent binary phase Cu5As2. Its formation occurs in strong competition with that of two other close neighboring solid-solution compounds, [Cu3−x(As1−ySby) (Cu3P-type; hP24, P63cm) and Cu3−x(As,Sb) (Cu9TeSb2-type; cP32, Pm−3n)], reflecting a complex interplay between composition, solubility ranges and thermal history. No evidence for the existence of high-temperature (HT) and low-temperature (LT) polymorphic phases was found for either the binary compound Cu5As2 or the ternary compound Cu5(As,Sb)2. Electrical resistivity measurements on a quenched sample indicate metallic behavior. These findings provide new insight into phase stability and structure–property relationships in Cu-As-Sb alloys and contribute to the understanding of competing intermetallic phases in this system.
Open AccessPhase Stability and Competing Crystal Structures in the Formation of the Intermetallic Compounds Cu5As2 and Cu5(As,Sb)2
An experimental investigation of the Cu-As-Sb ternary system in the Cu-rich region led to the identification of a new intermetallic phase, Cu5(As,Sb)2. The compound crystallizes in the orthorhombic Mg5Ga2-type structure (oI28, Ibam), analogous to the binary parent phase Cu5As2, with lattice parameters a = 5.968–5.977(1) Å, b = 11.550–11.565(3) Å, c = 5.530–5.573(3) Å. Similar to the parent Cu5As2 phase, the ternary compound forms with slight Cu under stoichiometry and exhibits a limited compositional range, with no continuous solid solubility between the binary and ternary phases. The phase formation, compositional stability, and decomposition behavior were systematically studied using a combination of powder and single-crystal X-ray diffraction (XRD, including Rietveld refinement), metallographic analysis with optical and scanning electron microscopy with energy-dispersive X-ray spectroscopy (LOM, SEM-EDXS), electron backscatter diffraction (EBSD) and thermal analysis (DTA, DSC). The results reveal that Cu5(As,Sb)2 is a high-temperature phase forming peritectically at 650–635 °C and stable only within a limited temperature interval. No continuous solid solubility exists between the ternary compound and the parent binary phase Cu5As2. Its formation occurs in strong competition with that of two other close neighboring solid-solution compounds, [Cu3−x(As1−ySby) (Cu3P-type; hP24, P63cm) and Cu3−x(As,Sb) (Cu9TeSb2-type; cP32, Pm−3n)], reflecting a complex interplay between composition, solubility ranges and thermal history. No evidence for the existence of high-temperature (HT) and low-temperature (LT) polymorphic phases was found for either the binary compound Cu5As2 or the ternary compound Cu5(As,Sb)2. Electrical resistivity measurements on a quenched sample indicate metallic behavior. These findings provide new insight into phase stability and structure–property relationships in Cu-As-Sb alloys and contribute to the understanding of competing intermetallic phases in this system.
- Top Cited PapersOpen Access
- 24 December 2025
- Published by Springer Nature in The European Physical Journal C
- Vol. 85 (12)
Future Circular Collider Feasibility Study Report
Volume 1 of the FCC Feasibility Report presents an overview of the physics case, experimental programme, and detector concepts for the Future Circular Collider (FCC). This volume outlines how FCC would address some of the most profound open questions in particle physics, from precision studies of the Higgs and EW bosons and of the top quark, to the exploration of physics beyond the Standard Model. The report reviews the experimental opportunities offered by the staged implementation of FCC, beginning with an electron-positron collider (FCC-ee), operating at several centre-of-mass energies, followed by a hadron collider (FCC-hh). Benchmark examples are given of the expected physics performance, in terms of precision and sensitivity to new phenomena, of each collider stage. Detector requirements and conceptual designs for FCC-ee experiments are discussed, as are the specific demands that the physics programme imposes on the accelerator in the domains of the calibration of the collision energy, and the interface region between the accelerator and the detector. The report also highlights advances in detector, software and computing technologies, as well as the theoretical tools/reconstruction techniques that will enable the precision measurements and discovery potential of the FCC experimental programme. The content and structure of this report are guided by the scope and priorities defined in the mandate of the FCC Feasibility Study. It is therefore not intended to serve as an exhaustive review of the full physics potential of FCC. Several topics, already covered in earlier reports such as the FCC CDR, are not reiterated here or are addressed only briefly, in alignment with the study’s focus. This volume reflects the outcome of a global collaborative effort involving hundreds of scientists and institutions, aided by a dedicated community-building coordination, and provides a targeted assessment of the scientific opportunities and experimental foundations of the FCC programme.
- 24 December 2025
- Published by Springer Nature in The European Physical Journal C
- Vol. 85 (12)
Top Cited PapersOpen AccessFuture Circular Collider Feasibility Study Report
Volume 1 of the FCC Feasibility Report presents an overview of the physics case, experimental programme, and detector concepts for the Future Circular Collider (FCC). This volume outlines how FCC would address some of the most profound open questions in particle physics, from precision studies of the Higgs and EW bosons and of the top quark, to the exploration of physics beyond the Standard Model. The report reviews the experimental opportunities offered by the staged implementation of FCC, beginning with an electron-positron collider (FCC-ee), operating at several centre-of-mass energies, followed by a hadron collider (FCC-hh). Benchmark examples are given of the expected physics performance, in terms of precision and sensitivity to new phenomena, of each collider stage. Detector requirements and conceptual designs for FCC-ee experiments are discussed, as are the specific demands that the physics programme imposes on the accelerator in the domains of the calibration of the collision energy, and the interface region between the accelerator and the detector. The report also highlights advances in detector, software and computing technologies, as well as the theoretical tools/reconstruction techniques that will enable the precision measurements and discovery potential of the FCC experimental programme. The content and structure of this report are guided by the scope and priorities defined in the mandate of the FCC Feasibility Study. It is therefore not intended to serve as an exhaustive review of the full physics potential of FCC. Several topics, already covered in earlier reports such as the FCC CDR, are not reiterated here or are addressed only briefly, in alignment with the study’s focus. This volume reflects the outcome of a global collaborative effort involving hundreds of scientists and institutions, aided by a dedicated community-building coordination, and provides a targeted assessment of the scientific opportunities and experimental foundations of the FCC programme.
- 22 September 2025
- Published by American Physical Society (APS) in Physical Review B
- Vol. 112 (12)
Leading role of Dirac cones in transport properties of LaFeAsO
- 22 September 2025
- Published by American Physical Society (APS) in Physical Review B
- Vol. 112 (12)
Leading role of Dirac cones in transport properties of LaFeAsO
- 8 February 2025
- Published by Springer Nature in Journal of Materials Science
- Vol. 60 (8) , 3940-3956
The new PrNi6Si6 intermetallic: from crystal structure to thermal and electrical transport properties across a wide temperature range (2–900 K)
- 8 February 2025
- Published by Springer Nature in Journal of Materials Science
- Vol. 60 (8) , 3940-3956
The new PrNi6Si6 intermetallic: from crystal structure to thermal and electrical transport properties across a wide temperature range (2–900 K)
- 3 December 2024
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 36 (24) , 11833-11851
Zn2MnSbO6 and Zn2FeSbO6: Two New Polar High-Pressure Ordered Corundum-Type Compounds
- 3 December 2024
- Published by American Chemical Society (ACS) in Chemistry of Materials
- Vol. 36 (24) , 11833-11851
Zn2MnSbO6 and Zn2FeSbO6: Two New Polar High-Pressure Ordered Corundum-Type Compounds
- Open Access
- 31 October 2023
- Published by Elsevier in Journal of Alloys and Compounds
- Vol. 972
Magnetic structures and properties of new 1:1 MoB-type RCo0.6Ni0.4 and RCo0.5Ni0.5 (R = Tb, Dy, Ho): Structural transition induced by magnetic ordering
- 31 October 2023
- Published by Elsevier in Journal of Alloys and Compounds
- Vol. 972
Open AccessMagnetic structures and properties of new 1:1 MoB-type RCo0.6Ni0.4 and RCo0.5Ni0.5 (R = Tb, Dy, Ho): Structural transition induced by magnetic ordering
- Open Access
Cu3As: Uncommon Crystallographic Features, Low-Temperature Phase Transitions, Thermodynamic and Physical Properties
The formation and crystal structure of the binary Cu3As phase have been re-investigated. Some physical properties were then measured on both single crystal and polycrystalline bulk. Cu3As melts congruently at 835 °C. At room temperature (RT), this compound has been found to crystallize in the hexagonal Cu3P prototype (hP24, P63cm) with lattice parameters: a = 7.1393(1) Å and c = 7.3113(1) Å, rather than in the anti HoH3-type (hP24, P–3c1) as indicated in literature. A small compositional range of 74.0–75.5 at.% Cu (26.0–24.5 at.% As) was found for samples synthesized at 300 and 400 °C; a corresponding slight understoichiometry is found in one out of the four Cu atomic sites, leading to the final refined composition Cu2.882(1)As. The present results disprove a change in the crystal structure above RT actually reported in the phase diagram (from γ’ to γ on heating). Instead, below RT, at T = 243 K (−30 °C), a first-order structural transition to a trigonal low-temperature superstructure, LT-Cu3−xAs (hP72, P–3c1) has been found. The LT polymorph is metrically related to the RT one, having the c lattice parameter three times larger: a = 7.110(2) Å and c = 21.879(4) Å. Both the high- and low-temperature polymorphs are characterized by the presence of a tridimensional (3D) uncommon and rigid Cu sublattice of the lonsdaleite type (Cu atoms tetrahedrally bonded), which remains almost unaffected by the structural change(s), and characteristic layers of triangular ‘Cu3As’-units (each hosting one As atom at the center, interconnected each other by sharing the three vertices). The first-order transition is then followed by an additional structural change when lowering the temperature, which induces doubling of also the lattice parameter a. Differential scanning calorimetry nicely detects the first low-temperature structural change occurring at T = 243 K, with an associated enthalpy difference, ΔH(TR), of approximately 2 J/g (0.53 kJ/mol). Low-temperature electrical resistivity shows a typical metallic behavior; clear anomalies are detected in correspondence to the solid-state transformations. The Seebeck coefficient, measured as a function of temperature, highlights a conduction of n-type. The temperature dependence of the magnetic susceptibility displays an overall constant diamagnetic response.
Open AccessCu3As: Uncommon Crystallographic Features, Low-Temperature Phase Transitions, Thermodynamic and Physical Properties
The formation and crystal structure of the binary Cu3As phase have been re-investigated. Some physical properties were then measured on both single crystal and polycrystalline bulk. Cu3As melts congruently at 835 °C. At room temperature (RT), this compound has been found to crystallize in the hexagonal Cu3P prototype (hP24, P63cm) with lattice parameters: a = 7.1393(1) Å and c = 7.3113(1) Å, rather than in the anti HoH3-type (hP24, P–3c1) as indicated in literature. A small compositional range of 74.0–75.5 at.% Cu (26.0–24.5 at.% As) was found for samples synthesized at 300 and 400 °C; a corresponding slight understoichiometry is found in one out of the four Cu atomic sites, leading to the final refined composition Cu2.882(1)As. The present results disprove a change in the crystal structure above RT actually reported in the phase diagram (from γ’ to γ on heating). Instead, below RT, at T = 243 K (−30 °C), a first-order structural transition to a trigonal low-temperature superstructure, LT-Cu3−xAs (hP72, P–3c1) has been found. The LT polymorph is metrically related to the RT one, having the c lattice parameter three times larger: a = 7.110(2) Å and c = 21.879(4) Å. Both the high- and low-temperature polymorphs are characterized by the presence of a tridimensional (3D) uncommon and rigid Cu sublattice of the lonsdaleite type (Cu atoms tetrahedrally bonded), which remains almost unaffected by the structural change(s), and characteristic layers of triangular ‘Cu3As’-units (each hosting one As atom at the center, interconnected each other by sharing the three vertices). The first-order transition is then followed by an additional structural change when lowering the temperature, which induces doubling of also the lattice parameter a. Differential scanning calorimetry nicely detects the first low-temperature structural change occurring at T = 243 K, with an associated enthalpy difference, ΔH(TR), of approximately 2 J/g (0.53 kJ/mol). Low-temperature electrical resistivity shows a typical metallic behavior; clear anomalies are detected in correspondence to the solid-state transformations. The Seebeck coefficient, measured as a function of temperature, highlights a conduction of n-type. The temperature dependence of the magnetic susceptibility displays an overall constant diamagnetic response.
- 11 March 2023
- Published by Elsevier in Journal of Alloys and Compounds
- Vol. 948
Solubility limits, magnetic and magnetocaloric properties of MoB-type GdCoxNi1−x (0.47 ≤ x ≤ 0.72)
- 11 March 2023
- Published by Elsevier in Journal of Alloys and Compounds
- Vol. 948
Solubility limits, magnetic and magnetocaloric properties of MoB-type GdCoxNi1−x (0.47 ≤ x ≤ 0.72)