Przemyslaw Data

Prof. Dr. Przemyslaw Data

orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

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

Representative Publications

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18 July 2016 in Advanced Science
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Journal Article
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Fernando B. DiasFernando B. Dias
Fernando B. Dias
JSJose Santos
Jose Santos
DGDavid R. Graves
David R. Graves
PDPrzemyslaw Data
Przemyslaw Data
RJRoberto Shigueru Nobuyasu Jr
Roberto Shigueru Nobuyasu Jr
AMAndrew P. Monkman
Andrew P. Monkman
Here, a comprehensive photophysical investigation of a the emitter molecule DPTZ‐DBTO2, showing thermally activated delayed fluorescence (TADF), with near‐orthogonal electron donor (D) and acceptor (A) units is reported. It is shown that DPTZ‐DBTO2 has minimal singlet–triplet energy splitting due to its near‐rigid molecular geometry. However, the electronic coupling between the local triplet (3LE) and the charge transfer states, singlet and triplet, (1CT, 3CT), and the effect of dynamic rocking of the D–A units about the orthogonal geometry are crucial for efficient TADF to be achieved. In solvents with low polarity, the guest emissive singlet 1CT state couples directly to the near‐degenerate 3LE, efficiently harvesting the triplet states by a spin orbit coupling charge transfer mechanism (SOCT). However, in solvents with higher polarity the emissive CT state in DPTZ‐DBTO2 shifts below (the static) 3LE, leading to decreased TADF efficiencies. The relatively large energy difference between the 1CT and 3LE states and the extremely low efficiency of the 1CT to 3CT hyperfine coupling is responsible for the reduction in TADF efficiency. Both the electronic coupling between 1CT and 3LE, and the (dynamic) orientation of the D–A units are thus critical elements that dictate reverse intersystem crossing processes and thus high efficiency in TADF.

11 January 2017 in Chemical Science
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Journal Article
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MOMasato Okazaki
Masato Okazaki
YTYouhei Takeda
Youhei Takeda
PDPrzemyslaw Data
Przemyslaw Data
PPPiotr Pander
Piotr Pander
HHHeather Higginbotham
Heather Higginbotham
SMSatoshi Minakata
Satoshi Minakata
Novel U-shaped donor–acceptor–donor (D–A–D) π-conjugated multi-functional molecules comprising dibenzo[a,j]phenazine (DBPHZ) as an acceptor and phenothiazines (PTZ) as donors have been developed. Most importantly, the D–A–D compounds exhibit not only distinct tricolor-changeable mechanochromic luminescence (MCL) properties but also efficient thermally activated delayed fluorescence (TADF). Quantum chemical calculations, X-ray diffraction analysis, and systematic studies on the photophysical properties indicated that the “two-conformation-switchable” PTZ units play a highly important role in achieving multi-color-changing MCL. Time-resolved photophysical measurements revealed that the developed D–A–D compounds also exhibit efficient orange-TADF. Furthermore, organic light-emitting diode (OLED) devices fabricated with the new TADF emitters have achieved high external quantum efficiencies (EQEs) up to 16.8%, which significantly exceeds the theoretical maximum (∼5%) of conventional fluorescent emitters.

6 April 2016 in Angewandte Chemie International Edition
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Journal Article
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PDPrzemyslaw Data
Przemyslaw Data
PPPiotr Pander
Piotr Pander
MOMasato Okazaki
Masato Okazaki
YTYouhei Takeda
Youhei Takeda
SMSatoshi Minakata
Satoshi Minakata
AMAndrew P. Monkman
Andrew P. Monkman

8 August 2014 in Advanced Functional Materials
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Journal Article
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VJVygintas Jankus
Vygintas Jankus
PDPrzemyslaw Data
Przemyslaw Data
DGDavid Graves
David Graves
CMCallum McGuinness
Callum McGuinness
JSJose Santos
Jose Santos
AMAndrew P. Monkman
Andrew P. Monkman

13 April 2017 in Nature Communications
Verified
Journal Article
Open access
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MEMarc K. Etherington
Marc K. Etherington
FFFlavio Franchello
Flavio Franchello
JGJamie Gibson
Jamie Gibson
TNThomas Northey
Thomas Northey
JSJose Santos
Jose Santos
AMAndrew P. Monkman
Andrew P. Monkman
Regio- and conformational isomerization are fundamental in chemistry, with profound effects upon physical properties, however their role in excited state properties is less developed. Here two regioisomers of bis(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene-S,S-dioxide, a donor–acceptor–donor (D–A–D) thermally-activated delayed fluorescence (TADF) emitter, are studied. 2,8-bis(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene-S,S-dioxide exhibits only one quasi-equatorial conformer on both donor sites, with charge-transfer (CT) emission close to the local triplet state leading to efficient TADF via spin-vibronic coupling. However, 3,7-bis(10H-phenothiazin-10-yl)dibenzo[b,d]thiophene-S,S-dioxide displays both a quasi-equatorial CT state and a higher-energy quasi-axial CT state. No TADF is observed in the quasi-axial CT emission. These two CT states link directly to the two folded conformers of phenothiazine. The presence of the low-lying local triplet state of the axial conformer also means that this quasi-axial CT is an effective loss pathway both photophysically and in devices. Importantly, donors or acceptors with more than one conformer have negative repercussions for TADF in organic light-emitting diodes.

12 January 2016 in Advanced Optical Materials
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Journal Article
Closed access
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RJRoberto Shigueru Nobuyasu Jr
Roberto Shigueru Nobuyasu Jr
ZRZhongjie Ren
Zhongjie Ren
GGGareth C. Griffiths
Gareth C. Griffiths
ABAndrei S. Batsanov
Andrei S. Batsanov
PDPrzemyslaw Data
Przemyslaw Data
Fernando B. DiasFernando B. Dias
Fernando B. Dias