4.8 Article

Theoretical and Experimental Studies on the Ability of Intracrystalline Pores of β-La2(SO4)3 To Accommodate Various Gas Species with a Special Focus on Ammonia Insertion Behaviors

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 44, 页码 52793-52801

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c16750

关键词

gas adsorption; porous material; ammonia; thermochemical heat storage; thermodynamics; first-principles calculation; thermogravimetry

资金

  1. JSPS [17K17821, 19J15085]
  2. Grants-in-Aid for Scientific Research [19J15085, 17K17821] Funding Source: KAKEN

向作者/读者索取更多资源

beta-La-2(SO4)(3) is a microporous inorganic crystal capable of accommodating various hydrogen compound molecules, with NH3, H2O, and HF being energetically stable in the crystal. The insertion of NH3 proceeds in two steps, differing from the single step insertion of H2O.
beta-La-2(SO4)(3) is a microporous inorganic crystal with one-dimensional perforated pores where H2O molecules can be inserted. To evaluate the nature of the pores and extend the application range, we investigate the ability to accommodate various hydrogen compound molecules XHn (CH4, NH3, HF, H2S, HCl, and HI) by insertion. The stable structures of the XHn molecules in the pores of beta-La-2(SO4)(3) and the change in the Gibbs energy for XHn insertion Delta(insert)G (T) are estimated by firstprinciples calculations. The guest XHn molecules are stabilized by forming H-O and X-La bonds with the beta-La-2(SO4)(3) host structure. Based on the values of Delta(inser)tG (T), NH3, H2O, and HF are energetically stable in the crystal even above 0 degrees C. Correspondingly, thermogravimetry (TG) of beta-La-2(SO4)(3) in NH3, CH4, and CO2 gases revealed that NH3 can be inserted into beta-La-2(SO4)(3) below 360 degrees C, but CH4 and CO2 cannot. Unlike the case of H2O insertion, NH3 insertion proceeds via two steps. The first step is a single-solid-phase reaction of beta-La-2(SO4)(3)center dot yNH(3), where NH3 molecules are inserted into the host structure with a continuously changing nonstoichiometric y value between 0 and 0.1. The second step is a two-solid-phase reaction between beta-La-2(SO4) 3.0.1-NH3 and beta'-La-2(SO4)(3)center dot 0.3NH(3), which is a phase formed after further NH3 insertion into beta-La-2(SO4)(3)center dot 0.1NH(3) with a minor change in the host structure. The fact that both NH3 and H2O can be inserted confirms that the pores of beta-La-2(SO4)(3) allow for the insertion of molecules with a strong polarity. This nature is similar to zeolites and metal-organic frameworks (MOFs) with polar surfaces in the pores.

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