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Organic metal halide hybrids with low-dimensional structures at the molecular level have received great attention recently for their exceptional structural tunability and unique photophysical properties. Here we report for the first time the synthesis and characterization of a one-dimensional (1D) organic metal halide hybrid, which contains metal halide nanoribbons with a width of three octahedral units. It is found that this material with a chemical formula C 8 H 28 N 5 Pb 3 Cl 11 shows a dual emission with a photoluminescence quantum efficiency (PLQE) of around 25%. Photophysical studies and density functional theory (DFT) calculations suggest the coexisting of delocalized free excitons and localized self-trapped excitons in metal halide nanoribbons leading to the dual emission. 

A supercapacitor requires two electronic conductors with large surface areas, separated by an ionic conductor. Here we demonstrate a method to print a highly stretchable supercapacitor. We formulate an ink by mixing graphene flakes and carbon nanotubes with an organic solvent, and use the ink to print two interdigitated electronic conductors on the surface of a dielectric elastomer. We then submerge the printed electronic conductors in an aqueous solution of monomer, photoinitiator, crosslinker, and salt. The organic solvent and water form a binary solvent in which the ions are mobile. Upon UV irradiation, a polymer network forms. In each printed electrode, the graphene flakes and carbon nanotubes form a percolating network, which interpenetrates the polymer network. The electronic and ionic conductors form large interfacial areas. When the supercapacitor is stretched, the graphene flakes and carbon nanotubes slide relative to one another, and the polymer network deforms by entropic elasticity. The polymer network traps individual graphene flakes and carbon nanotubes, so that repeated stretch neither breaks the percolating network nor shorts the two electrodes. The supercapacitor maintains 88% the initial capacitance after 1600 cycles of stretch to five times its initial dimension. The interpenetration of a covalent network of elastic polymer chains and a percolating network of conductive particles is generally applicable for making stretchable ionotronic devices. 

The photophysical properties of square planar Pt(II) complexes are often strongly dependent on their self‐assembly modes and intermolecular Pt⋯Pt interactions. Controlling these interactions is important to achieve valuable properties for various applications, such as light‐emitting diodes and environmental sensing devices. Herein, a series of highly luminescent ionic Pt(II) complexes with tunable emission colors are reported, by controlling the molecular structures and interactions in solid state. Four ionic Pt(II) complexes, with a general formula [Pt(C^{^}N)(N^{^}N)]⁺X⁻(C^{^}N = 2‐phenylpyridine or 2‐(2,4‐difluorophenyl)pyridine; N^{^}N = 2,2′‐bipyridine; X⁻= chloride (Cl⁻) or tetraphenylborate (BPh₄⁻), are designed, synthesized, and characterized. Due to the presence of intermolecular Pt⋯Pt interactions, strong metal–metal‐to‐ligand charge transfer (MMLCT) emissions are recorded in all four complexes with color changing from green to deep red in solid state. A high photoluminescence quantum efficiency (PLQE) of 81% is achieved for one of the complexes containing large BPh₄⁻anions, due to the site isolation effects. Detailed structural and photophysical characterizations reveal a clear correlation between the stacking of these Pt(II) complexes and their photophysical properties, which can be well regulated by the molecular structures and counter‐anions.