Joanna Kuncewicz

Dr. Joanna Kuncewicz


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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31 October 2014 in Chemical Communications
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JKJoanna Kuncewicz
Joanna Kuncewicz
Bunsho OhtaniBunsho Ohtani
Bunsho Ohtani
Titania particles modified with an extremely small amount (<0.01 mol%) of a rhodium species exhibited photocatalytic activity for the oxidative decomposition of acetaldehyde in air under visible-light irradiation. The reaction proceeded via a two-photon band-gap excitation mechanism with a built-in Rh(III)–Rh(IV) redox couple.

15 August 2016 in RSC Advances
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JKJoanna Kuncewicz
Joanna Kuncewicz
Bunsho OhtaniBunsho Ohtani
Bunsho Ohtani
Visible light-induced redox reactions of low-concentration rhodium-introduced titania proceeded through two photoexcitation of rhodium(iii) to the conduction band of titania and an electron in the valence band to thus-generated rhodium(iv).

5 June 2025 in ACS Applied Energy Materials
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MPMilda Petruleviciene
Milda Petruleviciene
KSKaja Spilarewicz
Kaja Spilarewicz
ISIrena Savickaja
Irena Savickaja
JJJurga Juodkazyte
Jurga Juodkazyte
JKJoanna Kuncewicz
Joanna Kuncewicz
Arũnas RamanavičiusArũnas Ramanavičius
Arũnas Ramanavičius

6 July 2020 in The Analyst
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PLPieter van Dalen Luna
Pieter van Dalen Luna
LMLukasz Majchrzak
Lukasz Majchrzak
Kamilla MalekKamilla Malek
Kamilla Malek
JKJoanna Kuncewicz
Joanna Kuncewicz
PMPawel Miskowiec
Pawel Miskowiec
In the pre-Hispanic Central Andes, the mummified bodies of ancestors stood as the basis for the social and cosmic order. This work discusses chemical compositions of the bodies determined by using molecular and elemental analytical methods.

15 February 2020 in Catalysts
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AJAgnieszka Jarosz-Duda
Agnieszka Jarosz-Duda
POPaulina O’callaghan
Paulina O’callaghan
JKJoanna Kuncewicz
Joanna Kuncewicz
PŁPrzemysław Łabuz
Przemysław Łabuz
WMWojciech Macyk
Wojciech Macyk
The core-shell NaYb0.99F4:Tm0.01@NaYF4 upconverting particles (UCPs) with a high UV emission to apply in NIR-driven photocatalysis were synthesized. The influence of the Yb3+ doping concentration in NaYxF4:Yb0.99−xTm0.01 core particles, and the role of the NaYF4 shell on the upconversion emission intensity of the UCPs were studied. The absorption of NIR light by the obtained UCPs was maximized by increasing the Yb3+ concentration in the core, reaching the maximum for Y3+-free particles (NaYb0.99F4:Tm0.01). Additionally, covering the NaYb0.99F4:Tm0.01 core with a protective layer of NaYF4 minimized the surface luminescence quenching, which significantly improved the efficiency of upconversion emission. The high intensity of the UV light emitted by the NaYb0.99F4:Tm0.01@NaYF4 under NIR irradiation resulted in a high photocatalytic activity of TiO2 (P25) mixed with the synthesized material.

19 November 2024 in RSC Advances
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POPaulina O'CAllaghan
Paulina O'CAllaghan
AJAgnieszka Jarosz-Duda
Agnieszka Jarosz-Duda
JKJoanna Kuncewicz
Joanna Kuncewicz
KDKrzysztof Dzierzega
Krzysztof Dzierzega
WMWojciech Macyk
Wojciech Macyk
Preparation of highly active core–shell/hybrid materials based on up-converting particles combined with semiconductors for photocatalytic application usually requires sophisticated and multi-step synthesis procedures. We propose a new design of a highly efficient NIR-driven photocatalytic system composed of spatially separated thin films of upconverting NaYF4:Yb,Tm particles (UCPs), and TiO2. Several samples of UCPs were prepared in the form of thin films and suspensions, directly coated with a titania layer or mixed with P25. Photocatalytic and photoelectrochemical studies have shown that thin film samples achieved significantly higher photocatalytic activity than their suspended counterparts. Moreover, the sample consisting of spatially separated layers of UCPs and P25 presented a significant photocatalytic activity and generated the highest photocurrent intensity. Separating the photocatalyst and upconverter layers allows for an interchangeable photocatalytic system active in a wide range of light.