Chiral Stacking Identification of Two-Dimensional Triclinic Crystals Enabled by Machine Learning.
He HaoKangshu LiXujing JiXiaoxu ZhaoLianming TongJin ZhangPublished in: ACS nano (2024)
Chiral materials possess broken inversion and mirror symmetry and show great potential in the application of next-generation optic, electronic, and spintronic devices. Two-dimensional (2D) chiral crystals have planar chirality, which is nonsuperimposable on their 2D enantiomers by any rotation about the axis perpendicular to the substrate. The degree of freedom to construct vertical stacking of 2D monolayer enantiomers offers the possibility of chiral manipulation for designed properties by creating multilayers with either a racemic or enantiomerically pure stacking order. However, the rapid recognition of the relative proportion of two enantiomers becomes demanding due to the complexity of stacking orders of 2D chiral crystals. Here, we report the unambiguous identification of racemic and enantiomerically pure stackings for layered ReSe 2 and ReS 2 using circular polarized Raman spectroscopy. The chiral Raman response is successfully manipulated by the enantiomer proportion, and the stacking orders of multilayer ReSe 2 and ReS 2 can be completely clarified with the help of second harmonic generation and scanning transmission electron microscopy measurements. Finally, we trained an artificial intelligent Spectra Classification Assistant to predict the chirality and the complete crystallographic structures of multilayer ReSe 2 from a single circular polarized Raman spectrum with the accuracy reaching 0.9417 ± 0.0059.
Keyphrases
- capillary electrophoresis
- raman spectroscopy
- machine learning
- mass spectrometry
- electron microscopy
- ionic liquid
- room temperature
- deep learning
- magnetic resonance imaging
- gold nanoparticles
- body composition
- artificial intelligence
- optical coherence tomography
- climate change
- quantum dots
- reduced graphene oxide
- optic nerve