Dye-sensitized solar cells fabricated using ordered arrays of titania nanotubes (tube lengths 5, 10, and 20 microm) grown on titanium have been characterized by a range of experimental methods. The collection efficiency for photoinjected electrons in the cells is close to 100% under short circuit conditions, even for a 20 microm thick nanotube array. Transport, trapping, and back transfer of electrons in the nanotube cells have been studied in detail by a range of complementary experimental techniques. Analysis of the experimental results has shown that the electron diffusion length (which depends on the diffusion coefficient and lifetime of the photoinjected electrons) is of the order of 100 microm in the titania nanotube cells. This is consistent with the observation that the collection efficiency for electrons is close to 100%, even for the thickest (20 microm) nanotube films used in the study. The study revealed a substantial discrepancy between the shapes of the electron trap distributions measured experimentally using charge extraction techniques and those inferred indirectly from transient current and voltage measurements. The discrepancy is resolved by introduction of a numerical factor to account for non-ideal thermodynamic behavior of free electrons in the nanostructured titania.
The performance of perovskite solar cells recently exceeded 15% solar-to-electricity conversion efficiency for small-area devices. The fundamental properties of the active absorber layers, hybrid organic-inorganic perovskites formed from mixing metal and organic halides [e.g., (NH4)PbI3 and (CH3NH3)PbI3], are largely unknown. The materials are semiconductors with direct band gaps at the boundary of the first Brillouin zone. The calculated dielectric constants and band gaps show an orientation dependence, with a low barrier for rotation of the organic cations. Due to the electric dipole of the methylammonium cation, a photoferroic effect may be accessible, which could enhance carrier collection
We have developed a charge transport model that explicitly accounts for ion migration. This model has been used to interpret measured current–voltage characteristics that show hysteresis.
Thin
film lead halide perovskite cells, where the perovskite layer is deposited
directly onto a flat titania blocking layer, have reached AM 1.5 efficiencies
of over 15%, showing that the mesoporous
scaffold used in early types of perovskite solar cells is not essential.
We used a variety of techniques to gain a better understanding of
thin film perovskite cells prepared by a solution-based method. Twelve
cells were studied, which showed AM 1.5 efficiencies of ∼11%.
The properties of the cells were investigated using impedance spectroscopy,
intensity-modulated photovoltage spectroscopy (IMVS), intensity-modulated
photocurrent spectroscopy (IMPS), and open-circuit photovoltage decay
(OCVD). Despite the fact that all 12 cells were prepared at the same
time under nominally identical conditions, their behavior fell into
two distinct groups. One half of the cells exhibited ideality factors of m ≈
2.5, and the other half showed ideality factors of m ≈ 5. Impedance spectroscopy carried out under illumination
at open circuit for a range of intensities showed that the cell capacitance
was dominated by the geometric capacitance of the perovskite layer
rather than the chemical or diffusion capacitance due to photogenerated
carriers. The voltage dependence of the recombination resistance gave
ideality factors similar to those derived from the intensity dependence
of the open-circuit voltage. The IMVS time constant was determined
by the product of the geometric capacitance and the recombination
resistance. The two types of cells gave very different OCVD responses.
The cells with m ≈ 2.5 showed a persistent
photovoltage effect that was absent in the case of the cells with
higher ideality factors. The IMPS responses provide evidence of minor
efficiency losses by recombination under short-circuit conditions.
We present a dynamical Monte Carlo study of the dependence of the internal quantum efficiency (IQE) of an organic bulk heterojunction solar cell on the device morphology. The IQE is found to be strongly sensitive to the scale of phase separation in the morphology, with a peak at approximately 20 nm for the PFB/F8BT system studied. An ordered, checkered morphology exhibits a peak IQE 1.5 times higher than a disordered blend.
A greater
understanding of the structure–property relationships
of hybrid perovskites for solar cells is crucial for enhancing their
performance. The low-temperature phases of formamidinium lead iodide
(FAPbI3) have been investigated using rapid neutron powder
diffraction. On cooling, the metastable α-polymorph descends
in symmetry from the cubic unit cell phase present at room temperature
through two successive phase transitions. Between 285 and 140 K a
tetragonal phase, adopting the space group P4/mbm, is confirmed and the orientation of the disordered
FA cation over this temperature range determined. The cation dynamics
have also been investigated, over the same temperature range, at the
atomic scale by using ab initio molecular dynamics
simulations, which indicate contrasting FA motion in the cubic and
tetragonal structures. Below 140 K the neutron powder diffraction
data display weak Bragg scattering intensities not immediately indexable
to a related unit cell. Data collected at 100 K from N-deuterated
FAPbI3 did not reveal any indication of the fundamental
Bragg reflections at high d-spacing expected for
an expanded supercell model as previously reported. Other hypotheses
of a mixture of phases or a simple tetragonal cell below 140 K are
also rejected on the basis of the observed data, and our observations
are consistent with a locally disordered low-temperature γ-phase.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.