TY - JOUR
T1 - Van der Waals Layered Chiral Structure with Alkali Cation Exchange in LiInP2S6
AU - Qian, Eric K.
AU - Nag, Jadupati
AU - Sarker, Saugata
AU - Waters, Michael J.
AU - Gopalan, Venkatraman
AU - Rondinelli, James M.
AU - Kanatzidis, Mercouri G.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/10/8
Y1 - 2024/10/8
N2 - In this study, we report the multiple synthesis routes and characterization of two-dimensional (2D) bimetallic thiophosphate, LiInP2S6, achieved through direct combination and P2S5 reactive flux methods. This material features a noncentrosymmetric space group (P312) and exhibits weak van der Waals forces between its layers. Differential thermal analysis indicated a congruent melting point of 785 °C. Structural characterization via single-crystal X-ray diffraction revealed detailed insights into its lattice configuration. Optoelectronic properties were assessed using UV-vis spectroscopy, showing a bandgap of 3.07 eV, and photoemission yield spectroscopy in air (PYSA), which determined a work function of 5.74 eV. Notably, despite the lithium ions being embedded and immobile within the layers rather than being loose in the interlayer space, the material exhibits significant alkali cation exchange capabilities. This happens by dislodging lithium ions from the intralayer space to the interlayer space and then exchanging them with incoming alkali ions. Experiments demonstrated interlayer expansion and significant ion exchange when exposed to Na+, K+, Rb+, and Cs+ ions, suggesting potential applications in ion exchange and encapsulation technologies. This work expands the compositional space for 2D layered thiophosphates, highlighting their promise for next-generation electronic devices and heavy metal remediation.(Figure presented).
AB - In this study, we report the multiple synthesis routes and characterization of two-dimensional (2D) bimetallic thiophosphate, LiInP2S6, achieved through direct combination and P2S5 reactive flux methods. This material features a noncentrosymmetric space group (P312) and exhibits weak van der Waals forces between its layers. Differential thermal analysis indicated a congruent melting point of 785 °C. Structural characterization via single-crystal X-ray diffraction revealed detailed insights into its lattice configuration. Optoelectronic properties were assessed using UV-vis spectroscopy, showing a bandgap of 3.07 eV, and photoemission yield spectroscopy in air (PYSA), which determined a work function of 5.74 eV. Notably, despite the lithium ions being embedded and immobile within the layers rather than being loose in the interlayer space, the material exhibits significant alkali cation exchange capabilities. This happens by dislodging lithium ions from the intralayer space to the interlayer space and then exchanging them with incoming alkali ions. Experiments demonstrated interlayer expansion and significant ion exchange when exposed to Na+, K+, Rb+, and Cs+ ions, suggesting potential applications in ion exchange and encapsulation technologies. This work expands the compositional space for 2D layered thiophosphates, highlighting their promise for next-generation electronic devices and heavy metal remediation.(Figure presented).
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U2 - 10.1021/acs.chemmater.4c01876
DO - 10.1021/acs.chemmater.4c01876
M3 - Article
AN - SCOPUS:85205906020
SN - 0897-4756
VL - 36
SP - 9718
EP - 9728
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 19
ER -