Andrew Clive Grimsdale

Dr. Andrew Clive Grimsdale

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Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

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

Representative Publications

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2 March 1998 in Angewandte Chemie International Edition
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Journal Article
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AKArno Kraft
Arno Kraft
AGAndrew Clive Grimsdale
Andrew Clive Grimsdale
AHAndrew B. Holmes
Andrew B. Holmes

19 February 2009 in Chemical Reviews
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Journal Article
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AGAndrew Clive Grimsdale
Andrew Clive Grimsdale
KCKhai Leok Chan
Khai Leok Chan
RMRainer E. Martin
Rainer E. Martin
PJPawel G. Jokisz
Pawel G. Jokisz
AHAndrew B. Holmes
Andrew B. Holmes

16 January 2001 in Journal of the American Chemical Society
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Journal Article
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SSSepas Setayesh
Sepas Setayesh
AGAndrew Clive Grimsdale
Andrew Clive Grimsdale
TWTanja Weil
Tanja Weil
VEVolker Enkelmann
Volker Enkelmann
KMKlaus Müllen
Klaus Müllen
GLGünther Leising
Günther Leising

18 December 2014 in Journal of Materials Chemistry A
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Journal Article
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TSTeddy Salim
Teddy Salim
SSShuangyong Sun
Shuangyong Sun
YAYuichiro Abe
Yuichiro Abe
AKAnurag Krishna
Anurag Krishna
AGAndrew Clive Grimsdale
Andrew Clive Grimsdale
YLYeng-Ming Lam
Yeng-Ming Lam
This review provides an overview of factors affecting film morphology and how together with device architecture they impact perovskite cell performance.

3 July 2015 in Journal of Materials Chemistry A
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Journal Article
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TKTeck Ming Koh
Teck Ming Koh
TKThirumal Krishnamoorthy
Thirumal Krishnamoorthy
NYNatalia Yantara
Natalia Yantara
CSChen Shi
Chen Shi
WLWei Lin Leong
Wei Lin Leong
NMNripan Mathews
Nripan Mathews
A lead-free low bandgap organic–inorganic hybrid perovskite, formamidinium tin iodide, is utilized as a light absorbing layer in photovoltaics. This material has a bandgap of 1.41 eV which allows light harvesting from the near infrared region, making high photocurrents achievable. A power conversion efficiency of 2.10% was accomplished upon incorporating SnF2.

2 February 2010 in Chemical Society Reviews
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Journal Article
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JLJiaoli Li
Jiaoli Li
AGAndrew Clive Grimsdale
Andrew Clive Grimsdale
Polymers based upon 2,7-disubstituted carbazole have recently become of great interest as electron-donating materials in organic photovoltaic devices. In this tutorial review the synthesis of such polymers and their relative performances in such devices are surveyed. In particular structure–property relationships are investigated and the potential for the rational design of materials for high efficiency solar cells is discussed. In the case of the 2,7-carbazole homopolymer it has been found that electron acceptors other than fullerenes produce higher energy conversion efficiencies. To get around possible problems with the build-up of charge density at the 3- and 6-positions and to improve the solar light harvesting ability of the polymers by reducing the bandgap, ladder- and step-ladder type 2,7-carbazole polymers have been synthesised. The fully ladderised polymers gave very poor results in devices, but efficiencies of over 1% have been obtained from a step-ladder polymer with a diindenocarbazole monomer unit. Donor–acceptor copolymers containing 2,7-carbazole donors and various electron-accepting comonomer units have been prepared. An efficiency of 6% has been reported from a device using such a copolymer and by suitable choice of the acceptor comonomer, polymers can be designed with potential theoretical power conversion efficiencies of 10%. While such efficiencies remain to be obtained, the results to date certainly suggest that carbazole-based polymers and copolymers are among the most promising materials yet proposed for obtaining high efficiency organic solar cells.