Abstract

Unusual adsorption phenomena, such as breathing and negative gas adsorption (NGA), are rare and challenge our thermodynamic understanding of adsorption in deformable porous solids. In particular, NGA appears to break the rules of thermodynamics in these materials by exhibiting a spontaneous release of gas accompanying an increase in pressure. This anomaly relies on long-lived metastable states. A fundamental understanding of this process is desperately required for the discovery of new materials with this exotic property. Interestingly, NGA was initially observed upon adsorption of methane at relatively low temperature, close to the respective standard boiling point of the adsorptive, and no NGA was observed at elevated temperatures. In this contribution, we present an extensive investigation of adsorption of an array of gases at various temperatures on DUT-49, a material which features an NGA transition. Experiments, featuring a wide range of gases and vapors at temperatures ranging from 21-308 K, were used to identify for each guest a critical temperature range in which NGA can be detected. The experimental results were complemented by molecular simulations that help to rationalize the absence of NGA at elevated temperatures, and the non-monotonic behavior present upon temperature decrease. Furthermore, this in-depth analysis highlights the crucial thermodynamic and kinetic conditions for NGA, which are unique to each guest and potentially other solids with similar effects. We expect this exploration to provide detailed guidelines for experimentally discovering NGA and related "rule breaking" phenomena in novel and already known materials, and provide the conditions required for the application of this effect, for example as pressure amplifying materials.

Highlights

  • Structural exibility and so ness in porous crystals has generated new adsorption phenomena beyond the classi ed types of isotherms known for rigid adsorbents.[1]

  • In 2016, we discovered the phenomenon of negative gas adsorption (NGA), initially observed in the metal–organic frameworks (MOFs) DUT-49 (Dresden University of Technology No 49, general formula [Cu2(C40H20N2O8)], rst reported in ref. 22), which is characterized by a negative step in the adsorption isotherm originating from adsorptioninduced structural contraction of the pores.[23]

  • The shape and p–T range in which structural contraction occurs are similar for both materials, with the exception that a small range at the lower edge of the phase diagram shows the presence of NGA in DUT49, experimentally not observed for MIL-53 so far

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Summary

Introduction

Structural exibility and so ness in porous crystals has generated new adsorption phenomena beyond the classi ed types of isotherms known for rigid adsorbents.[1]. To investigate whether the non-monotonic evolution of DnNGA as a function of temperature is universal, the study on adsorption of methane was extended by rst analysing a series of hydrocarbons and hydrogen at their respective standard boiling points or below (ESI Fig. 1†).

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