Natalia Martsinovich

Dr. Natalia Martsinovich

Department of Chemistry, The University of Sheffield, Sheffield, UK
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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2 June 2017 in Energy & Environmental Science
Verified
Journal Article
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YWYiou Wang
Yiou Wang
MBMustafa Kemal Bayazit
Mustafa Kemal Bayazit
SMSavio J. A. Moniz
Savio J. A. Moniz
QRQiushi Ruan
Qiushi Ruan
CLChi Ching Lau
Chi Ching Lau
JTJunwang Tang
Junwang Tang
A linker-controlled strategy has been demonstrated to synthesize polymeric photocatalysts for efficient H 2 evolution by UV-Vis-IR with benchmark quantum yields.

21 September 2011 in Energy & Environmental Science
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Journal Article
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NMNatalia Martsinovich
Natalia Martsinovich
ATAlessandro Troisi
Alessandro Troisi
A full understanding of the elementary processes taking place in dye-sensitised solar cells requires an accurate description of the electronic structure of the dyes, the semiconductor surface, the electrolyte and their interactions. This review describes how electronic structure calculations have contributed to the field since its first steps and what methodologies have been adopted to study the charge transfer processes at the interface. Not all properties are equally predictable with electronic structure methods, and this work highlights the main success areas (e.g. the rationalization of the optical properties of the dyes), the recent developments (e.g. the improved description of the dye–semiconductor interaction) and the key challenges for the future (e.g. the calculation of charge recombination rate).

22 May 2012 in The Journal of Physical Chemistry Letters
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FAFrancesco Ambrosio
Francesco Ambrosio
NMNatalia Martsinovich
Natalia Martsinovich
ATAlessandro Troisi
Alessandro Troisi

6 December 2010 in The Journal of Physical Chemistry C
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Journal Article
Closed access
NMNatalia Martsinovich
Natalia Martsinovich
DJDaniel R. Jones
Daniel R. Jones
ATAlessandro Troisi
Alessandro Troisi

8 July 2005 in Science
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Pavel TroshinPavel Troshin
Pavel Troshin
AAAnthony G. Avent
Anthony G. Avent
ADAdam D. Darwish
Adam D. Darwish
NMNatalia Martsinovich
Natalia Martsinovich
AAAla'A K. Abdul-Sada
Ala'A K. Abdul-Sada
RTRoger Taylor
Roger Taylor
Fluorination of C 60 at 550°C leads to milligram quantities of two stable fullerene derivatives with 58-carbon cage structures: C 58 F 18 and C 58 F 17 CF 3 . The compounds were characterized by mass spectrometry and fluorine nuclear magnetic resonance spectroscopy, and the data support a heptagonal ring in the framework. The resulting strain, which has hindered past attempts to prepare these smaller quasi-fullerenes, is mitigated here by hybridization change of some of the carbons in the pentagons from sp 2 to sp 3 because of fluorine addition. The loss of carbon from C 60 is believed to occur via sequential fluorine addition to a C–C single bond and an adjacent C[dbond]C bond, followed by loss of a :CF 2 carbene.

20 May 2011 in The Journal of Physical Chemistry C
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Journal Article
Closed access
NMNatalia Martsinovich
Natalia Martsinovich
ATAlessandro Troisi
Alessandro Troisi