resumo
The zeolitic imidazolate framework-8 (ZIF-8) combines a significantly high microporosity with an excellent thermal, chemical, and hydrothermal stability. Here, we demonstrated that ZIF-8 can display significant levels of protonic conductivity through a water-mediated surface transport mechanism associated to the presence of di-coordinated Zn ions revealed by X-ray photoelectron spectroscopy. A set of powders with particle sizes from 2.8 mu m down to 80 nm studied by dynamic water vapour sorption analysis was used to demonstrate that water adsorbs predominantly in the micropore cavities of microcrystalline ZIF-8, whereas adsorption on the external surface becomes the dominant contribution for the nanostructured material. Impedance spectroscopy in turn revealed that the protonic conductivity of the nanocrystalline ZIF-8 was two orders of magnitude higher than that of the micron-sized powders, reaching approximately 0.5 mS.cm(-1) at 94 degrees C and 98% relative humidity. Simple relations were derived in order to estimate the potential gains in water uptake and conductivity as a function of the particle size. This new strategy combining particle nanostructuring with surface defects, demonstrated here for one of the most know metal organic framework, is of general application to potentially boost the conductivity of other materials avoiding chemical functionalization strategies that in most if not all cases compromise their chemical stability, particularly under high humidity and high temperature conditions.
palavras-chave
METAL-ORGANIC FRAMEWORKS; ZEOLITIC IMIDAZOLATE FRAMEWORKS; EXTERNAL SURFACE; STABILITY; ADSORPTION; SEPARATION; XPS
categoria
Science & Technology - Other Topics; Materials Science
autores
Munoz-Gil, D; Figueiredo, FML
nossos autores
Grupos
G1 - Materiais Porosos e Nanossistemas
G3 - Materiais Eletroquímicos, Interfaces e Revestimentos
Projectos
agradecimentos
This work was funded through projects UniRCell (SAICTPAC/0032/2015, POCI-01-0145-FEDER-016422) and CICECO-Aveiro Institute of Materials (UID/CTM/50011/2019), financed by national funds through the FCT/MEC, and when applicable, co-financed by FEDER under the PT2020 Partnership Agreement.