We describe the structural and chemical properties of gold halide perovskites (Cs2AuIAuIIIX6, X = I, Br, Cl) synthesized at low temperatures. Photoluminescence shows bandgaps (1–1.4 eV), highlighting their potential for optoelectronic devices.
This study introduces a novel approach for developing DNA-functionalized gold nanoparticles (AuNPs) that respond to disease-specific factors and microenvironmental changes, achieving an effective anti-tumor effect through photothermal therapy.
Inorganic gold halide perovskites, owing to their excellent stability and tunable bandgaps, are poised to serve as environmentally benign alternatives to lead halide perovskites in the field of energy conversion applications.
This perspective highlights the potential of gold(II) complexes in catalysis, shedding light on the pivotal roles played by mononuclear and dinuclear gold(II) complexes, whether as isolated entities or proposed intermediates, in catalytic reactions.
Regular and robust 2D conjugated organogold networks with anthra-tetrathiophene repeat units are synthesized by debrominative coupling on iodine-passivated Au(111). Dynamic error correction becomes feasibly through iodine-induced bond reversibility.