As the biocompatible materials, hydrogels have been widely used in three- dimensional (3D) bioprinting/organ printing to load cell for tissue engineering. It is important to precisely control hydrogels deposition during printing the mimic organ structures. However, the printability of hydrogels about printing parameters is seldom addressed. In this paper, we systemically investigated the printability of hydrogels from printing lines (one dimensional, 1D structures) to printing lattices/films (two dimensional, 2D structures) and printing 3D structures with a special attention to the accurate printing. After a series of experiments, we discovered the relationships between the important factors such as air pressure, feedrate, or even printing distance and the printing quality of the expected structures. Dumbbell shape was observed in the lattice structures printing due to the hydrogel diffuses at the intersection. Collapses and fusion of adjacent layer would result in the error accumulation at Z direction which was an important fact that could cause printing failure. Finally, we successfully demonstrated a 3D printing hydrogel scaffold through harmonize with all the parameters. The cell viability after printing was compared with the casting and the results showed that our bioprinting method almost had no extra damage to the cells.

Circularly polarized luminescent (CPL) materials are promising in applications such as 3D displays and quantum communication. Hybrid organic–inorganic copper­(I) iodides have been rapidly developed due to their intense photoluminescence and structural diversity; nevertheless, the reported Cu–I clusters rarely show CPL activities. In this study, we introduced chiral organic molecules R/S-methylbenzylammonium (R/S-MBA) into Cu–I inorganic skeletons to achieve chiral tetranuclear (R/S-MBA)4Cu4I4 clusters with intense orange luminescence and CPL activity at room temperature. These enantiomeric (R/S-MBA)4Cu4I4 clusters show oppositely signed circular dichroism (CD) signals, which agree well with their simulated electronic CD spectra. The crystallization-induced helical arrangement of (R/S-MBA)4Cu4I4 clusters and their largely distorted polynuclear configuration demonstrate a new platform for the study of chiral-related properties.

The discovery of new halide perovskite-type structures could favor the exploration of optoelectronic materials, as in the case of double perovskites applied in solar cells, light-emitting diodes, and X-ray detectors. In this work, we propose a strategy for designing quadruple perovskites by heterovalent cation transmutation from double perovskites. Two stable quadruple perovskite halides, i.e., Cs4CdSb2Cl12 and Cs4CdBi2Cl12, with a vacancy-ordered three-dimensional (3D) crystal structure were predicted through symmetry analysis and density functional theory (DFT) calculations. The title perovskite halides are also electronically 3D with direct forbidden bandgaps. Following the indication provided by the DFT results, Cs4CdSb2Cl12 and Cs4CdBi2Cl12 as unique quadruple perovskites were successfully synthesized by a solvothermal method. The steady-state photoluminescence (PL) shows wide emission, while the transient PL exhibits carrier recombination lifetime on the order of microseconds at low temperature. The quadruple perovskite halides provide an alternative platform for promising optoelectronic material design in addition to simple and double perovskites.