Umberto Anselmi-Tamburini

Prof. Umberto Anselmi-Tamburini

University of Pavia
orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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30 October 2020 in ACS Applied Materials & Interfaces
Verified
Journal Article
Open access
PGPaolo Ghigna
Paolo Ghigna
LAL. Airoldi
L. Airoldi
MFMartina Fracchia
Martina Fracchia
DCDaniele Callegari
Daniele Callegari
Umberto Anselmi-TamburiniUmberto Anselmi-Tamburini
Umberto Anselmi-Tamburini
Eliana  QuartaroneEliana Quartarone
Eliana Quartarone
High-entropy oxides based on transition metals, such as Mg0.2Co0.2Ni0.2Cu0.2Zn0.2O (TM-HEO), have recently drawn special attention as potential anodes in lithium-ion batteries due to high specific capacity and cycling reversibility. However, the lithiation/delithiation mechanism of such systems is still controversial and not clearly addressed. Here, we report on an operando XAS investigation into TM-HEO-based anodes for lithium-ion cells during the first lithiation/delithiation cycle. This material showed a high specific capacity exceeding 600 mAh g–1 at 0.1 C and Coulombic efficiency very close to unity. The combination of functional and advanced spectroscopic studies revealed complex charging mechanisms, developing through the reduction of transition-metal (TM) cations, which triggers the conversion reaction below 1.0 V. The conversion is irreversible and incomplete, leading to the final collapse of the HEO rock-salt structure. Other redox processes are therefore discussed and called to account for the observed cycling behavior of the TM-HEO-based anode. Despite the irreversible phenomena, the HEO cubic structure remains intact for ∼60% of lithiation capacity, so proving the beneficial role of the configuration entropy in enhancing the stability of the HEO rock-salt structure during the redox phenomena.

20 April 2020 in The Journal of Physical Chemistry Letters
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Journal Article
Open access
MFMartina Fracchia
Martina Fracchia
PGPaolo Ghigna
Paolo Ghigna
TPTommaso Pozzi
Tommaso Pozzi
Umberto Anselmi-TamburiniUmberto Anselmi-Tamburini
Umberto Anselmi-Tamburini
VCValentina Colombo
Valentina Colombo
PTPiero Torelli
Piero Torelli
The mechanisms of CO oxidation on the Mg0.2Co0.2Ni0.2Cu0.2Zn0.2O high entropy oxide were studied by means of operando soft X-ray absorption spectroscopy. We found that Cu is the active metal, and that Cu(II) can be rapidly reduced to Cu(I) by CO when the temperature is larger than 130 °C. Co and Ni do not have any role in this respect. The Cu(II) oxidation state can be easily but slowly recovered by treating the sample in O2 at ca. 250 °C. However, it should be noted that CuO is readily and irreversibly reduced to Cu(I) if treated in CO at T>100 °C. Thus, the main conclusion of this work is that the high configurational entropy of Mg0.2Co0.2Ni0.2Cu0.2Zn0.2O stabilizes the rock-salt structure and permits the oxidation/reduction of Cu to be reversible, thus permitting the catalytic cycle to take place.

23 June 2017 in Materials Science and Technology
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Journal Article
Open access
Umberto Anselmi-TamburiniUmberto Anselmi-Tamburini
Umberto Anselmi-Tamburini
JGJ. R. Groza
J. R. Groza
The interest towards field-assisted sintering techniques has been growing rapidly in the last 20 years, particularly in applications involving hard to sinter materials, such as nanocrystalline, refractory, and metastable materials. These techniques, in fact, allow obtaining the densification in conditions that are considerably milder than in traditional pressureless sintering or in hot-pressing. Despite this success, there is still a poor understanding of the involved basic mechanisms. In this assessment, all the main aspects associated with the use of these technique will be presented and discussed, with particular emphasis on spark plasma sintering.

26 February 2021 in Biology
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Journal Article
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IPIan Postuma
Ian Postuma
SGSara González
Sara González
MHMaria S Herrera
Maria S Herrera
LPLucas Provenzano
Lucas Provenzano
MFMichele Ferrarini
Michele Ferrarini
Silva BortolussiSilva Bortolussi
Silva Bortolussi
(1) Background:The quality of neutron beams for Boron Neutron Capture Therapy (BNCT) is currently defined by its physical characteristics in air. Recommendations exist to define whether a designed beam is useful for clinical treatment. This work presents a new way to evaluate neutron beams based on their clinical performance and on their safety, employing radiobiological quantities. (2) Methods: The case study is a neutron beam for deep-seated tumors from a 5 MeV proton beam coupled to a beryllium target. Physical Figures of Merit were used to design five beams; however, they did not allow a clear ranking of their quality in terms of therapeutic potential. The latter was then evaluated based on in-phantom dose distributions and on the calculation of the Uncomplicated Tumor Control Probability (UTCP). The safety of the beams was also evaluated calculating the in-patient out-of-beam dosimetry. (3) Results: All the beams ensured a UTCP comparable to the one of a clinical beam in phantom; the safety criterion allowed to choose the best candidate. When this was tested in the treatment planning of a real patient treated in Finland, the UTCP was still comparable to the one of the clinical beam. (4) Conclusions: Even when standard physical recommendations are not met, radiobiological and dosimetric criteria demonstrate to be a valid tool to select an effective and safe beam for patient treatment.

15 April 2020 in Batteries & Supercaps
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Journal Article
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LALorenzo Airoldi
Lorenzo Airoldi
Umberto Anselmi-TamburiniUmberto Anselmi-Tamburini
Umberto Anselmi-Tamburini
BVBarbara Vigani
Barbara Vigani
Silvia RossiSilvia Rossi
Silvia Rossi
Piercarlo MustarelliPiercarlo Mustarelli
Piercarlo Mustarelli
Eliana  QuartaroneEliana Quartarone
Eliana Quartarone

1 August 2002 in Journal of Materials Research
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Journal Article
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FMFilippo Maglia
Filippo Maglia
Chiara MilaneseChiara Milanese
Chiara Milanese
Umberto Anselmi-TamburiniUmberto Anselmi-Tamburini
Umberto Anselmi-Tamburini
SDStefania Doppiu
Stefania Doppiu
GCGiorgio Cocco
Giorgio Cocco