Two-Dimensional Metal-Organic Frameworks with Unique Oriented Layers for Oxygen Reduction Reaction: Tailoring the Activity through Exposed Crystal FacetsShow others and affiliations
2022 (English)In: CCS CHEMISTRY, ISSN 2096-5745, Vol. 4, no 5, p. 1633-1642Article in journal (Refereed) Published
Abstract [en]
As one of the most important families of porous materials, metal-organic frameworks (MOFs) have well-defined atomic structures. This provides ideal models for investigating and understanding the relationships between structures and catalytic activities at the molecular level. However, the active sites on the edges of two-dimensional (2D) MOFs have rarely been studied, as they are less exposed to the surfaces. Here, for the first time, we synthesized and observed that the 2D layers could align perpendicular to the surface of a 2D zeolitic imidazolate framework L (ZIF-L) with a leaf-like morphology. Owing to this unique orientation, the active sites on the edges of the 2D crystal structure could mostly be exposed to the surfaces. Interestingly, when another layer of ZIF-L-Co was grown heteroepitaxially onto ZIF-L-Zn (ZIF-L-Zn@ZIF-L-Co), the two layers shared a common b axis but rotated by 90 degrees in the ac plane. This demonstrated that we could control exposed facets of the 2D MOFs. The ZIF-L-Co with more exposed edge active sites exhibited high electrocatalytic activity for oxygen reduction reaction. This work provides a new concept of designing unique oriented layers in 2D MOFs to expose more edge-active sites for efficient electrocatalysis. [GRAPHICS] .
Place, publisher, year, edition, pages
Chinese Chemical Society , 2022. Vol. 4, no 5, p. 1633-1642
Keywords [en]
unique oriented layer, two-dimensional material, metal-organic framework, electrocatalyst, oxygen reduction reaction
National Category
Inorganic Chemistry Materials Chemistry
Identifiers
URN: urn:nbn:se:kth:diva-314224DOI: 10.31635/ccschem.022.202101666ISI: 000794318300018Scopus ID: 2-s2.0-85129869648OAI: oai:DiVA.org:kth-314224DiVA, id: diva2:1671383
Note
QC 20220617
2022-06-172022-06-172023-06-08Bibliographically approved