"Breathing" organic cation to stabilize multiple structures in low-dimensional Ge-, Sn-, and Pb-based hybrid iodide perovskites. Issue 19 (12th August 2022)

• Record Type: Journal Article
• Authors: Chen, Congcong; Morgan, Emily E.; Liu, Yang; Chen, Jian; Seshadri, Ram; Mao, Lingling
• Is Part Of: Inorganic chemistry frontiers. Volume 9:Issue 19(2022)
• Page Start: 4892
• Page End: 4898
• Publication Date: 2022-08-12
• Subjects: Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d2qi01247b
• Languages: English
• ISSNs: 2052-1553

Abstract

Abstract : By using S-(2-aminoethyl)isothiouronium (ETU) as the templating cation, five new metal iodide hybrids, (ETU)GeI4, (ETU)4 Ge5 I18, (ETU)PbI4 and (ETU)3 Pb2 I10 are reported with varied C–S–C angles in the organic cation. Abstract : Low-dimensional hybrid inorganic–organic perovskites are excellent candidates for stable optoelectronic devices. The dimensionality of these perovskites depends largely on the organic and inorganic compositions, as well as the synthetic conditions. Here, we report five new hybrid iodides, (ETU)4 Ge5 I18, (ETU)GeI4, (ETU)SnI4, (ETU)PbI4, and (ETU)3 Pb2 I10 using only one type of organic cation, namely, S-(2-aminoethyl)isothiouronium (ETU). (ETU)GeI4 and (ETU)SnI4 belong to the (110)-oriented structure-type with "3 × 3" sawtooth corrugated layers and crystallize in a structure with the orthorhombic space group Pbca . (ETU)4 Ge5 I18 crystallizes in a structure with the triclinic space group P 1̄, featuring a 2D layered structure with combinations of corner, edge, and face-sharing [GeI6 ] octahedra. For the Pb-based series, (ETU)PbI4 has the conventional (100) – oriented 2D type whereas (ETU)3 Pb2 I10 has a unique 0D structure. Remarkably, the unstable 2D orange-phase (ETU)PbI4 transforms to a stable 0D yellow phase (ETU)3 Pb2 I10, accompanied by the reduction of the C–S–C angle of the organic cation ETU. The optical band gaps are largely regulated by the diverse types of structure and are in the range of 1.8 eV to 2.8 eV. (ETU)SnI4 is the only material showing notable photoluminescence at room-temperature. Our work showcases the flexibility of the organic cation in determining the structural dimensionality and provides a new strategy in generating new hybrid materials.