| Literature DB >> 31393726 |
Ryo Sasai1, Hiroaki Sato1, Mako Sugata1, Takuya Fujimura1, Shinsuke Ishihara2, Kenzo Deguchi3, Shinobu Ohki3, Masataka Tansho3, Tadashi Shimizu3, Naoto Oita4, Mako Numoto5, Yasuhiro Fujii4,5, Shogo Kawaguchi6, Yoshiki Matsuoka7, Koki Hagura6,7, Tomohiro Abe7, Chikako Moriyoshi7.
Abstract
Layered double hydroxides (LDHs) are promising compounds in a wide range of fields. However, exchange of CO32- anions with other anions is necessary, because the CO32- anions are strongly affixed in the LDH interlayer space. To elucidate the reason for the extremely high stability of CO32- anions intercalated in LDHs, we investigated in detail the chemical states of CO32- anions and hydrated water molecules in the LDH interlayer space by synchrotron radiation X-ray diffraction, solid-state NMR spectroscopy, and Raman spectroscopy. We found the rigidity of the network structure formed between the CO32- anions, hydrated water molecules, and the hydroxyl groups on the metal hydroxide layer surface to be a crucial factor underlying the stability of CO32- anions in the LDH interlayer space.Entities:
Year: 2019 PMID: 31393726 DOI: 10.1021/acs.inorgchem.9b01365
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165