Crystal structure, electronic structure, and optical properties of the novel Li4CdGe2S7, a wide‐bandgap quaternary sulfide with a polar structure derived from lonsdaleite. Issue 9 (22nd August 2022)

• Record Type: Journal Article
• Authors: Craig, Andrew J.; Shin, Seung Han; Cho, Jeong Bin; Balijapelly, Srikanth; Kelly, Jordan C.; Stoyko, Stanislav S.; Choudhury, Amitava; Jang, Joon I.; Aitken, Jennifer A.
• Is Part Of: Acta crystallographica. Volume 78:Issue 9(2022)
• Page Start: 470
• Page End: 480
• Publication Date: 2022-08-22
• Subjects: crystal structure -- thiogermanate -- diamond‐like -- wide bandgap -- lonsdaleite -- quaternary sulfide; Crystallography -- Periodicals; Crystals -- Periodicals; 548.3
• DOI: 10.1107/S2053229622008014
• Languages: English
• ISSNs: 2053-2296

Abstract

Abstract : The novel quaternary thiogermanate Li4 CdGe2 S7 was discovered from a solid‐state reaction at 750 °C. The compound adopts the Cu5 Si2 S7 structure type, which is a derivative of lonsdaleite. Li4 CdGe2 S7 appears to be a better IR nonlinear optical candidate than Li2 CdGeS4 and one of the most promising contenders to date. Abstract : The novel quaternary thiogermanate Li4 CdGe2 S7 (tetralithium cadmium digermanium heptasulfide) was discovered from a solid‐state reaction at 750 °C. Single‐crystal X‐ray diffraction data were collected and used to solve and refine the structure. Li4 CdGe2 S7 is a member of the small, but growing, class of I4 –II–IV2 –VI7 diamond‐like materials. The compound adopts the Cu5 Si2 S7 structure type, which is a derivative of lonsdaleite. Crystallizing in the polar space group Cc, Li4 CdGe2 S7 contains 14 crystallographically unique ions, all residing on general positions. Like all diamond‐like structures, the compound is built of corner‐sharing tetrahedral units that create a relatively dense three‐dimensional assembly. The title compound is the major phase of the reaction product, as evidenced by powder X‐ray diffraction and optical diffuse reflectance spectroscopy. While the compound exhibits a second‐harmonic generation (SHG) response comparable to that of the AgGaS2 (AGS) reference material in the IR region, its laser‐induced damage threshold (LIDT) is over an order of magnitude greater than AGS for λ = 1.064 µm and τ = 30 ps. Bond valence sums, global instability index, minimum bounding ellipsoid (MBE) analysis, and electronic structure calculations using density functional theory (DFT) were used to further evaluate the crystal structure and electronic structure of the compound and provide a comparison with the analogous I2 –II–IV–VI4 diamond‐like compound Li2 CdGeS4 . Li4 CdGe2 S7 appears to be a better IR nonlinear optical (NLO) candidate than Li2 CdGeS4 and one of the most promising contenders to date. The exceptional LIDT is likely due, at least in part, to the wider optical bandgap of ∼3.6 eV.