Snaith group

Abstract:

Six dierbium carbide endohedral metallofullerenes have been synthesized and chromatographically isolated. Single-crystal X-ray diffractometry unambiguously ascertains their structures as Er₂C₂@C_2v(5)-C₈₀, Er₂C₂@C_s(6)-C₈₂, Er₂C₂@C_s(15)-C₈₄, Er₂C₂@C_2v(9)-C₈₆, Er₂C₂@C_s(15)-C₈₆, and Er₂C₂@C_s(32)-C₈₈, respectively. The Er···Er distances of the major erbium sites inside the C_s(6)-C₈₂, C_2v(5)-C₈₀, C_s(15)-C₈₄, C_s(15)-C₈₆, C_2v(9)-C₈₆, and C_s(32)-C₈₈ cages are 3.801, 3.860, 4.062, 4.066, 4.307, and 4.372 Å, respectively, which show a linear tendency with an increase in the major axis of the fullerene cages (8.064, 8.238, 8.508, 8.582, 8.815, and 8.953 Å, respectively). Furthermore, the electrochemical and molecular orbital analyses reveal that the redox chemistry of the Er₂C₂@C_80-88 isomers is associated with the carbon cage, which is different from the situations found for typical dimetallofullerenes, such as Y₂@C₈₂, Er₂@C_82-84, and Lu₂@C_82,86 isomers, which show metal-dependent oxidation processes, indicating the importance of C₂ insertion in carbide cluster metallofullerenes.

Abstract:

The excellent optoelectronic properties demonstrated by hybrid organic/inorganic metal halide perovskites are all predicated on precisely controlling the exact nucleation and crystallization dynamics that occur during film formation. In general, high‐performance thin films are obtained by a method commonly called solvent engineering (or antisolvent quench) processing. The solvent engineering method removes excess solvent, but importantly leaves behind solvent that forms chemical adducts with the lead‐halide precursor salts. These adduct‐based precursor phases control nucleation and the growth of the polycrystalline domains. There has not yet been a comprehensive study comparing the various antisolvents used in different perovskite compositions containing cesium. In addition, there have been no reports of solvent engineering for high efficiency in all‐inorganic perovskites such as CsPbI3. In this work, inorganic perovskite composition CsPbI3 is specifically targeted and unique adducts formed between CsI and precursor solvents and antisolvents are found that have not been observed for other A‐site cation salts. These CsI adducts control nucleation more so than the PbI2–dimethyl sulfoxide (DMSO) adduct and demonstrate how the A‐site plays a significant role in crystallization. The use of methyl acetate (MeOAc) in this solvent engineering approach dictates crystallization through the formation of a CsI–MeOAc adduct and results in solar cells with a power conversion efficiency of 14.4%.