TY - JOUR
T1 - Orbital Trap of Xenon
T2 - Driving Force Distinguishing between Xe and Kr Found at a Single Ag(I) Site in MFI Zeolite at Room Temperature
AU - Oda, Akira
AU - Kouzai, Hiroe
AU - Sawabe, Kyoichi
AU - Satsuma, Atsushi
AU - Ohkubo, Takahiro
AU - Gotoh, Kazuma
AU - Kuroda, Yasushige
N1 - Funding Information:
This work was supported by a Japan Society for the Promotion of Science (JSPS) Grant-in-Aid for Young Scientists (no. 20K15297) and ESICB (JPMXP0112101003). The authors thank Drs. Kazuhiko Fujie, Tatsuya Hidano, and Akihiko Nakamura as members of Taiyo Nippon Sanso Holdings Group for measuring breakthrough curves of Xe and Kr. They also thank Dr. Toshinori Mori for his kind assistance in collecting XAFS and Xe NMR spectra. They acknowledge Dr. Atsushi Itadani for his kind assistance in performing XAFS experiments. XAFS measurements were conducted at NW10A of Photon Factory Program Advisory Committee (proposal nos.: 2008G616, 2010G693). H.T. acknowledges the financial support (Research Fellowship for Young Scientists, DC1) from the JSPS. Financial supports were also provided by the Ministry of Education, Culture, Sports, Science and Technology of Japan: Grants-in-Aid for Scientific Research, nos. 21655021, 16H04118, and 19K05499. 129
Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022
Y1 - 2022
N2 - Noble gas (Ng) elements are stable because of their octet electronic configuration, and thus Ng capture and purification are highly challenging. Here, we show a new concept for these applications: an orbital trap for Xe. This concept was found in Xe adsorption/separation processes at room temperature (RT) at the single Ag(I) site in MFI zeolite. Experiments and calculations showed the zeolite lattice-coordinated Ag(I) single ion has excellent electron-accepting nature and thereby induces the Xe 5p → Ag(I) 5s donation orbital interaction, forming a stable σ-bond with Xe even in the lower-pressure region and at RT. By contrast, the stable σ-bond for Kr adsorption is not established at RT because of the instability of the orbital interactions of the Kr 4p → Ag(I) 5s donation, as reflected from the relatively high energy of the Kr 4p orbital. Thus, the single Ag(I) site allows it to distinguish between Xe and Kr at RT; the Xe separation from the Xe/Kr gas mixture was achieved at RT using the Ag/MFI containing a high concentration of single Ag(I) sites. Our findings suggest that the orbital Xe trap using the local structure of porous materials shows promise as an efficient approach to selectively collect Xe (air concentration 0.087 ppm only). It will help to expand the range of applications of the costly Xe.
AB - Noble gas (Ng) elements are stable because of their octet electronic configuration, and thus Ng capture and purification are highly challenging. Here, we show a new concept for these applications: an orbital trap for Xe. This concept was found in Xe adsorption/separation processes at room temperature (RT) at the single Ag(I) site in MFI zeolite. Experiments and calculations showed the zeolite lattice-coordinated Ag(I) single ion has excellent electron-accepting nature and thereby induces the Xe 5p → Ag(I) 5s donation orbital interaction, forming a stable σ-bond with Xe even in the lower-pressure region and at RT. By contrast, the stable σ-bond for Kr adsorption is not established at RT because of the instability of the orbital interactions of the Kr 4p → Ag(I) 5s donation, as reflected from the relatively high energy of the Kr 4p orbital. Thus, the single Ag(I) site allows it to distinguish between Xe and Kr at RT; the Xe separation from the Xe/Kr gas mixture was achieved at RT using the Ag/MFI containing a high concentration of single Ag(I) sites. Our findings suggest that the orbital Xe trap using the local structure of porous materials shows promise as an efficient approach to selectively collect Xe (air concentration 0.087 ppm only). It will help to expand the range of applications of the costly Xe.
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U2 - 10.1021/acs.jpcc.2c01515
DO - 10.1021/acs.jpcc.2c01515
M3 - Article
AN - SCOPUS:85130381379
SN - 1932-7447
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
ER -