Structural Dynamics of Metal Halide Perovskites during Photoinduced Halide Segregation.

Despite substantial research effort, photoinduced halide segregation in mixed halide perovskites continues to limit the available perovskite chemistries for use in optoelectronic applications. In this study, we present new insights into halide-segregation process through in situ X-ray diffraction measurements that reveal substantial structural changes in mixed-halide perovskites under excitation. We observe that photoinduced halide segregation leads to the formation of one iodide-rich and one bromide-rich perovskite composition whose Br:I ratios are the same (at 20 and 93% bromine, respectively), for a range of compositions of the pristine initial perovskite phase.

In Situ Measurement of Electric-Field Screening in Hysteresis-Free PTAA/FACsPb(IBr)/C60 Perovskite Solar Cells Gives an Ion Mobility of ∼3 × 10 cm/(V s), 2 Orders of Magnitude Faster than Reported for Metal-Oxide-Contacted Perovskite Cells with Hysteresis.

We apply a series of transient measurements to operational perovskite solar cells of the architecture ITO/PTAA/FACsPb(IBr)/C60/BCP/Ag, and similar cells with FAMA. The cells show no detectable JV hysteresis. Using photocurrent transients at applied bias we find a ∼1 ms time scale for the electric field screening by mobile ions in these cells.

Terahertz Emission from Hybrid Perovskites Driven by Ultrafast Charge Separation and Strong Electron-Phonon Coupling.

Unusual photophysical properties of organic-inorganic hybrid perovskites have not only enabled exceptional performance in optoelectronic devices, but also led to debates on the nature of charge carriers in these materials. This study makes the first observation of intense terahertz (THz) emission from the hybrid perovskite methylammonium lead iodide (CH NH PbI ) following photoexcitation, enabling an ultrafast probe of charge separation, hot-carrier transport, and carrier-lattice coupling under 1-sun-equivalent illumination conditions. Using this approach, the initial charge separation/transport in the hybrid perovskites is shown to be driven by diffusion and not by surface fields or intrinsic ferroelectricity.

Perovskite-perovskite tandem photovoltaics with optimized band gaps.

We demonstrate four- and two-terminal perovskite-perovskite tandem solar cells with ideally matched band gaps. We develop an infrared-absorbing 1.2-electron volt band-gap perovskite, FACsSnPbI, that can deliver 14.

Cesium Lead Halide Perovskites with Improved Stability for Tandem Solar Cells.

A semiconductor that can be processed on a large scale with a bandgap around 1.8 eV could enable the manufacture of highly efficient low cost double-junction solar cells on crystalline Si. Solution-processable organic-inorganic halide perovskites have recently generated considerable excitement as absorbers in single-junction solar cells, and though it is possible to tune the bandgap of (CH3NH3)Pb(BrxI1-x)3 between 2.

Transparency and damage tolerance of patternable omniphobic lubricated surfaces based on inverse colloidal monolayers.

A transparent coating that repels a wide variety of liquids, prevents staining, is capable of self-repair and is robust towards mechanical damage can have a broad technological impact, from solar cell coatings to self-cleaning optical devices. Here we employ colloidal templating to design transparent, nanoporous surface structures. A lubricant can be firmly locked into the structures and, owing to its fluidic nature, forms a defect-free, self-healing interface that eliminates the pinning of a second liquid applied to its surface, leading to efficient liquid repellency, prevention of adsorption of liquid-borne contaminants, and reduction of ice adhesion strength.

Liquid-infused structured surfaces with exceptional anti-biofouling performance.

Bacteria primarily exist in robust, surface-associated communities known as biofilms, ubiquitous in both natural and anthropogenic environments. Mature biofilms resist a wide range of antimicrobial treatments and pose persistent pathogenic threats. Treatment of adherent biofilm is difficult, costly, and, in medical systems such as catheters or implants, frequently impossible.