期刊
JOURNAL OF SOLID STATE CHEMISTRY
卷 324, 期 -, 页码 -出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2023.124070
关键词
Metal-organic framework; Proton conductivity; -SO3H group; Ligand exchange
Herein, a series of Zr(IV)-MOFs (Zr-(NDC)(x)(SNDC)(1-x)) based on 1,4-naphthalenedicarboxylic acid (H2NDC) and 6-sulfonate-1,4-naphthalenedicarboxylic acid (H3SNDC) were constructed using the postsynthetic ligand exchange process. Functional sulfonic acid groups were anchored in the pores of the MOFs. Among them, Zr-(NDC)(0.3)(SNDC)(0.7) exhibited exceptional proton conductivity of 3.18 x 10(-4) S cm(-1) at 90 degrees C and 98% relative humidity (RH), which was significantly higher than pristine Zr-NDC. This work demonstrates a facile in situ ligand exchange approach for constructing functional group modified MOFs with high proton conductivity.
Herein, the postsynthetic ligand exchange process was adopted to construct a series of 1,4-naphthalenedicarboxylic acid (H2NDC) and 6-sulfonate-1,4-naphthalenedicarboxylic acid (H3SNDC) based Zr(IV)-MOFs (Zr-(NDC)(x)(SNDC)(1-x)). This strategy anchored functional sulfonic acid groups in the pore of the MOFs. Among them, Zr-(NDC)(0.3)(SNDC)(0.7) exhibited outstanding proton conductivity of 3.18 x 10(-4) S cm(-1) at 90 degrees C and 98% relative humidity (RH), which was approximately three orders of magnitude greater than that of pristine Zr-NDC. This work demonstrated a facile in situ ligand exchange approach for constructing functional group modified MOFs with high proton conductivity.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据