Recently, two‐dimensional (2D) structure on three‐dimensional (3D) perovskites (graded 2D/3D) has been reported to be effective in significantly improving both efficiency and stability. However, the electrical properties of the 2D structure as a passivation layer on the 3D perovskite thin film and resistance to the penetration of moisture may vary depending on the length of the alkyl chain. In addition, the surface defects of the 2D itself on the 3D layer may also be affected by the correlation between the 2D structure and the hole conductive material. Therefore, systematic interfacial study with the alkyl chain length of long‐chained alkylammonium iodide forming a 2D structure is necessary. Herein, the 2D interfacial layers formed are compared with butylammonium iodide (BAI), octylammonium iodide (OAI), and dodecylammonium iodide (DAI) iodide on a 3D (FAPbI3)0.95(MAPbBr3)0.05 perovskite thin film in terms of the PCE and humidity stability. As the length of the alkyl chain increased from BA to OA to DA, the electron‐blocking ability and humidity resistance increase significantly, but the difference between OA and DA is not large. The PSC post‐treated with OAI has slightly higher PCE than those treated with BAI and DAI, achieving a certified stabilized efficiency of 22.9%.
Molecular engineering toward the structure of a passivation ligand is essential to improve the photoluminescence (PL) efficiency of perovskite nanocrystals (PNCs). To establish the surface recovery mechanism of red‐emitting CsPb(Br,I)3 NCs with PbI2 additives in the presence of a tightly bound passivation layer, time‐resolved photoluminescence (TRPL) measurements and their chemometric analysis are employed. Two quaternary alkylammonium ligands, didodecyldimethylammonium iodide (DDAI) and tridodecylmethylammonium iodide (TDAI), are used to form a passivation layer, and then their role in the surface defects recovery is investigated by varying the amount of PbI2 additives. It is found that the structural difference between DDAI and TDAI can affect the accessibility of PbI2 additives to surface defects. The TRPL spectra analysis reveals that the ligand passivation with DDAI does not induce discernible lifetime enhancement with using PbI2 additives, but only a non‐radiative pathway is gradually accelerated with increasing the amount of them. The TDAI ligand, however, shows the opposite behavior to give the best PL performance with a distinct molar ratio of TDAI:PbI2, even though the passivation itself gives a lower PL performance. It is argued that the intrinsic structural properties of the TDAI ligand are responsible for the effective surface recovery with the additives.
Local and general factors have been attributed to root resorption occurred by injuries such as trauma and dental caries that affect periodontal ligament or dental pulp tissue. Pathologic root resorption is different from physiologic root resorption in terms of resorption pattern such as micromorphology of resorption fossae and types of observed cells. Microscopic morphologies and histologic features of physiologic and pathologic root resorption surface of maxillary primary central incisors resulting from trauma and periapical inflammation were observed by scanning electron microscope and light microscope. The morphology of physiologic resorption lacunae was small and oval or circular shape with regularities. The morphology of pathologic resorption lacunae was large and polygonal shape with irregularities compared with the physiologic resorption lacunae. Multinucleated giant cells and mononuclear cells were closely attached to the physiologic and pathologic resorption lacunae, whereas several kinds of mesenchymal cells with numerous inflammatory cells were found in the areas adjacent to the pathologic resorption surface. Compensating cementum formation took place along some of the areas of physiologic and pathologic resorption area resulting from trauma, but could not be observed on pathologic resorption area resulting from periapical inflammation.
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