Bulk IrOOH can be chemically exfoliated into single layers, which act as highly active and stable electrocatalysts for oxygen evolution from water under acidic conditions.
Solid oxides with transition-metal ions in unusual oxidation states attract enormous attention due to their electronic, magnetic, and catalytic properties. Yet, no crystalline oxide compounds based on purely trivalent iridium have been characterized to date. Here, we present the synthesis and thorough investigation of the properties of the compounds K 0.75 Na 0.25 IrO 2 and IrOOH, both containing trivalent iridium on a triangular lattice in layers of [IrO 2 ] − . K 0.75 Na 0.25 IrO 2 crystallizes in a P2-structure with the space group P6 3 /mmc, while the crystal structure of IrOOH adopts the direct maximal subgroup P3̅ m1. The trivalent state of the iridium ion is discussed with regards to the iridium−oxygen bond length from X-ray diffraction, the chemical composition, the electronic and magnetic behavior of the material, and X-ray photoemission spectroscopy. The discovery of a new valence state in ternary crystalline iridium oxides is not only of interest from a fundamental perspective, but also has far-reaching implications for such diverse fields as electrochromism, solid-state magnetism, and especially heterogeneous catalysis.
A fibrillar, polymeric intermediate (Cd2Se)n was isolated from the synthesis of CdSe nanorods, which suggests that the reactants themselves can template anisotropic growth. It is shown that high monomer concentration is the principal factor favouring this reaction pathway. The intermediate is distinct from crystalline semiconductor or small clusters and is surprisingly temperature-stable below 250 °C.
Despite their outstanding photovoltaic performance, organic–inorganic perovskite solar cells still face severe stability issues and limitations in their device dimension. Further development of perovskite solar cells therefore requires a deeper understanding of loss mechanisms, in particular, concerning the origin and impact of trap states. Here, different surface properties of submicrometer sized CH3NH3PbI3 particles are studied as a model system by photoluminescence spectroscopy to investigate the impact of the perovskite crystal surface on photoexcited states. Comparison of single crystals with either isolating or electron‐rich surface passivation indicates the presence of positively charged surface trap states that can be passivated in case of the latter. These surface trap states cause enhanced nonradiative recombination at room temperature, which is a loss mechanism for solar cell performance. In the orthorhombic phase, the origin of multiple emission peaks is identified as the recombination of free and bound excitons, whose population ratio critically depends on trap state properties. The dynamics of exciton trapping at 50 K are observed on a time‐scale of tens of picoseconds by a simultaneous population decrease and increase of free and bound excitons, respectively. These results emphasize the potential of surface passivation to further improve the performance of perovskite solar cells.
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