An analytical method to characterize the crystal structure of layered double hydroxides: synthesis, characterization, and electrochemical studies of zinc-based LDH nanoplates

Due to their unique soft and complex structure, it has been difficult to analyze the exact crystal structure of layered double hydroxides (LDHs), which has been a major obstacle to understanding and improving the catalytic properties of LDHs. In this report, we present an analytical method to charac...

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Published inJournal of materials chemistry. A, Materials for energy and sustainability Vol. 8; no. 17; pp. 8692 - 8699
Main Authors Chung, Jiyong, Lee, Jaeyoung, Kim, Jae Kyeom, Kim, Minseong, Lee, Kug-Seung, Kim, Seung-Joo, Lee, Min Hyung, Yu, Taekyung
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 07.05.2020
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Summary:Due to their unique soft and complex structure, it has been difficult to analyze the exact crystal structure of layered double hydroxides (LDHs), which has been a major obstacle to understanding and improving the catalytic properties of LDHs. In this report, we present an analytical method to characterize the crystal structure of LDHs using Rietveld refinement, XPS, and XANES. Using this analytical method, we found that ZnCo LDH nanoplates prepared by a new facile synthetic route had a Zn 3.1 Co 1.9 Cl 2 (OH) 8 ·H 2 O structure and contained a large portion of divalent Co cations, unlike the previously reported ZnCo LDHs. Thanks to this accurate crystal structure analysis, we found that the cause of the enhanced electrochemical properties of the ZnCo LDH nanoplates toward the oxygen evolution reaction was the large portion of divalent Co cations. Due to their unique soft and complex structure, it has been difficult to analyze the exact crystal structure of layered double hydroxides (LDHs), which has been a major obstacle to understanding and improving the catalytic properties of LDHs.
Bibliography:10.1039/d0ta01774d
Electronic supplementary information (ESI) available. See DOI
ISSN:2050-7488
2050-7496
DOI:10.1039/d0ta01774d