Related Experiment Video
Updated: Jan 18, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
Martensite-like phase transformation of ligand-capped SnS tetrahedrons from π phase to α phase and its impact on H2
Xiangxin Du1, Kenji Kazumi1, Toru Utsunomiya1
1Department of Materials Science and Engineering, Kyoto University Sakyo-ku Kyoto 606-8501 Japan nose.yoshitaro.5e@kyoto-u.ac.jp.
Abstract:
π-Tin sulfide (SnS) is an emerging semiconductor of interest with attractive properties for applications in solar energy conversion and non-linear optics. However, its intrinsic metastability raises concerns and requires further investigation. Here, we report a newly discovered martensite-like phase transition in ligand-capped π-SnS tetrahedrons by a post-annealing treatment. By adjusting the annealing temperature, we found that the desorption of surface ligands initiated the rearrangement of surface atoms, thus triggering a chain phase transformation from π phase to α phase through the displacement of adjacent atoms. Large amounts of boundaries and stacking faults were present in this process, as shown from high-resolution transmission electron microscopy combined with selected area electron diffraction. Furthermore, X-ray diffraction, X-ray photoelectron spectroscopy, and Fourier-transform infrared spectroscopy showed that the initiation temperature for phase transition relies on surface ligands. Hexamethyldisilazane (HMDS)-capped tetrahedrons show higher stability against a temperature of 500 °C than oleylamine (OLA)-capped tetrahedrons due to the stronger interaction between HMDS ligands with SnS surface atoms. The mechanism involved in the ligand-affected structure evolution of π-SnS tetrahedrons and the corresponding H2 generation performance is discussed in detail.
More Related Videos
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
09:21Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Related Concept Videos
Thermal Sigmatropic Reactions: Overview
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in 1,5-hexadiene, referred...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Valence Bond Theory
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
Ziegler–Natta Chain-Growth Polymerization: Overview