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Cite this: Dalton Trans., 2012, 41, 10497
www.rsc.org/dalton PERSPECTIVE
Single source molecular precursor routes to lead chalcogenides†
Nathaniel Owusu Boadi,
a,b
Mohammad Azad Malik,
a
Paul O’Brien*
a
and Johannes A. M. Awudza
b
Received 18th April 2012, Accepted 20th June 2012
DOI: 10.1039/c2dt30849e
The use of single-source molecular precursors for lead chalcogenide thin films by CVD or as
nanoparticles by solution methods is reviewed. The potential applications of these materials in solar
energy are discussed along with the relative advantages of the various methods.
1. Introduction
There is considerable current interest in metal chalcogenides
(sulfides, selenides or tellurides) stemming from their useful
properties as thin films or in highly dispersed form.
1
Potential
applications of these materials are in devices such as solar cells
(II–VI and III–VI), infrared detectors (IV–VI) and in room-temp-
erature thermoelectric generators (V–VI). Simple, inexpensive
and environmentally benign protocols are needed that also
provide control over issues such as composition, size and mor-
phology; facilitating the use of these materials in light emitting
diodes, non-linear optics, lasers or solar cells.
2
Lead is classified as a borderline soft metal in the hard/soft
acid–base concept of Pearson
3
and shows a wide variety of
coordination numbers. Lead(IV) compounds are known to have
coordination numbers between 4 and 8, but the majority of them
have the coordination number four. Lead(II) can bind as few as
two and as many as 10 ligands, with preferred coordination
numbers of 4 or 6.
4
Lead(II) forms stable complexes with both
soft and hard donor atom ligands. In similar coordination
environments, the affinity of lead(II) towards sulfur-based
ligands tends to be higher than for harder oxygen- or nitrogen-
donor groups. Despite considerable study of the coordination
chemistry of lead(II) with S- or Se-donor atom ligands
5
the
rational design of complexes remains a challenge. Tuning of the
structure of the ligands to satisfy the coordination preferences
and requirements of the lead(II) atom is still not that well under-
stood;
6
the same is true in design of precursors for chalcogen-
ides. Lead(II) complexes with sulfur, selenium or tellurium donor
atom ligands have been studied widely during the last few
decades.
5
The reason for the sustained interest in these com-
pounds lies in their significant structural diversity and potential
for applications.
6
Lead chalcogenides in various forms with critical dimensions
on the order of nanometers have attracted considerable interest
because of their unique physical and chemical properties and
Nathaniel Owusu Boadi
Nathaniel Owusu Boadi is a
Lecturer of Inorganic and
Environmental Chemistry at the
Kwame Nkrumah University of
Science and Technology,
Kumasi, Ghana. He is currently
a beneficiary of the Royal
Society, Leverhulme Africa
Award Grant Scheme, pursuing
a collaborative research with
the School of Chemistry, Uni-
versity of Manchester, United
Kingdom, on synthesis of
new precursor materials for the
production of solar cells under the supervision of Prof.
Paul O’Brien.
Mohammad Azad Malik
Mohammad Azad Malik com-
pleted his PhD Degree at Uni-
versity of London in 1990 and
then worked as a research
fellow with Prof. Paul O’Brien
initially at Queen Mary Univer-
sity of London (1990–1995),
then at Imperial College
(1995–2000) and currently as a
senior research fellow in The
University of Manchester
(2000–). He has a wide range
of experience in designing and
synthesis of single source mol-
ecular precursors for II/VI, III/V, III/VI, and IV/VI semiconduc-
tors and preparation and characterization of thin films and
nanoparticles.
† Dedicated to Professor David Cole-Hamilton on the occasion of his
retirement and for his outstanding contribution to transition metal
catalysis.
a
Schools of Chemistry and Materials, The University of Manchester,
Oxford Road, Manchester, M13 9PL, UK.
E-mail: paul.obrien@manchester.ac.uk
b
Department of Chemistry, Kwame Nkrumah University of Science and
Technology, Kumasi, Ghana
This journal is © The Royal Society of Chemistry 2012 Dalton Trans., 2012, 41, 10497–10506 | 10497