Use of an ionic liquid [bmim][BF4] (bmim = 1-butyl-3-methylimidazolium) as solvent has resulted in the first extended coordination structure, the two-dimensional network [Cu(bpp)]BF4 [bpp = 1,3-bis(4-pyridyl)propane], produced via a solvothermal route.
Single
crystals of heterovalent Bi-doped CH3NH3PbCl3 perovskite have been successfully grown through
the inverse temperature crystallization method. Bandgap narrowing
of 300 meV (a 55 nm red-shifting absorption edge) is obtained for
the nominal 20% Bi-doped crystal with the host structure and the energy
at the top of the valence band invariable. It is observed that the
contact between the Au electrodes and single crystals transforms from
Ohmic to Schottky, and the conductivity increases with increasing
Bi doping level. By contrast, the Bi-doped CH3NH3PbCl3 thin films are also prepared, and the similar bandgap
narrowing is found, although the narrowing degree is less than that
in single crystals. This work has a comprehensive understanding of
Bi-doped single crystals and thin films, providing further optoelectronic
applications for these promising solution-processed hybrid perovskite
semiconductor materials.
Organic–inorganic
perovskites have attracted increasing
attention in recent years owing to their excellent optoelectronic
properties and photovoltaic performance. In this work, the prototypical
hybrid perovskite CH3NH3PbI3 is turned
into a ferromagnetic material by doping Mn, which enables simultaneous
control of both charge and spin of electrons. The room-temperature
ferromagnetism originates from the double exchange interaction between
Mn2+–I––Mn3+ ions. Furthermore, it is discovered that the magnetic field can
effectively modulate the photovoltaic properties of Mn-doped perovskite
films. The photocurrent of Mn-doped perovskite solar cells increases
by 0.5% under a magnetic field of 1 T, whereas the photocurrent of
undoped perovskite decreases by 3.3%. These findings underscore the
potential of Mn-doped perovskites as novel solution-processed ferromagnetic
material and promote their application in multifunctional photoelectric-magnetic
devices.
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