The crystal structure of a new perovskite material, (C₄H₈NH₂)PbI₃ was determined and illustrated by single crystal X-ray diffraction. UV spectra, photoluminescence and XRD results show it is a promising alternative to hybrid organic–inorganic perovskites due to it's good water resistance and suitable bandgap.

The commonly employed methyl-ammonium containing perovskites are unstable at high temperature or under moisture attack, thus limiting their commercial applications. To overcome this barrier, a new perovskite possessing both thermal stability and water resistance has been constructed, involving pyrrolidinium rings (CH₂)₄NH₂PbI₃ (PyPbI₃), through a simple solution-processing method. It presents not only prolonged moisture resistance and a favorable bandgap of 1.80 eV, as determined by P-XRD and UV absorption, but also excellent thermal stability, as verified via the in situ XRD technique. The new structure may be applicable to perovskite solar cells with improved thermal stability and water resistance.

Organic-inorganic hybrid halide perovskite solar cells (PSCs) have been a trending topic in recent years. Significant progress has been made to increase their power conversion efficiency (PCE) to more than 20%. However, the poor stability of PSCs in both working and non-working conditions results in rapid degradation through multiple environmental erosions such as water, heat, and UV light. Attempts have been made to resolve the rapid-degradation problems, including formula changes, transport layer improvements, and encapsulations, but none of these have effectively resolved the dilemma. This paper reports our findings on adding inorganic films as surface-passivation layers on top of the hybrid perovskite materials, which not only enhance stability by eliminating weak sites but also prevent water penetration by using a water-stable layer. The surface-passivated hybrid perovskite layer indicates a slight increase of bandgap energy (E_g = 1.76 eV), compared to the original methylammonium lead iodide (MAPbI_3, E_g = 1.61 eV) layer, allowing for more stable perovskite layer with a small sacrifice in the photoluminescence property, which represents a lower charge diffusion rate and higher bandgap energy. Our finding offers an alternative approach to resolving the low stability issue for PSC fabrication.