Bottleneck Effect Explained by Le Bail Refinements: Structure Transformation of Mg-CUK-1 by Confining H2O Molecules.

The structure transformation of Mg-CUK-1 due to the confinement of H2O molecules was investigated. Powder X-ray diffraction (PXRD) patterns were collected at different H2O loadings and the cell parameters of the H2O-loaded Mg-CUK-1 material were determined by the Le Bail strategy refinements. A bottleneck effect was observed when one hydrogen-bonded H2O molecule per unit cell (18% relative humidity (RH)) was confined within Mg-CUK-1, confirming the increase in the CO2 capture for Mg-CUK-1.

1. Introduction

Global warming is one of the greatest risks to human civilization. In particular, the growing levels of anthropogenic carbon dioxide (CO2) emissions from fossil fuel combustion [1] directly influence our environment, triggering the continuous rise of temperatures across the planet. Only in 2017, worldwide CO2 emissions from fossil fuel combustion augmented by approximately 2% compared with the 2015–2016 period [2]. Currently, governments are working together on a worldwide basis to encourage the development of new technologies for a more efficient and effective CO2 capture [3]. Porous metal–organic frameworks (MOFs) or porous coordination polymers (PCPs) are among the most promising candidates for CO2 capture because their carbon dioxide sorption properties can be more broadly tuned than classical mesoporous materials (e.g., zeolites) [4]. Current synthetic approaches to further increase sorption selectivity towards carbon monoxide include the incorporation of open metal sites that can enhance molecular sorption, and by functionalizing the organic linker with the Lewis basic groups (e.g., amines and alcohols) [5]. Very recently, thorough investigations were also made to enhance the CO2 capture of MOFs by using the synergistic effects caused by pre-confining small amounts of polar molecules in their pores [6,7,8]. In this regard, we previously showed that the confinement of small amounts of H2O in a series of MOFs (functionalized with hydroxo functional groups, μ2-OH) steadily resulted in improved CO2 capture properties [9]. The confined H2O molecules are well-ordered in the pore-structure of these μ2-OH functionalized MOFs, working as preferential adsorption sites for the subsequent CO2 molecules [10]. In this communication, we describe the structure transformation of Mg-CUK-1 (CUK for Cambridge University–KRICT, see SM, Figure S1) [11] due to the confined H2O molecules within its pores, which previously demonstrated enhanced CO2 capture properties [12,13].

2. Materials and Methods

2.1. Material Synthesis

Mg-CUK-1 = [Mg3(OH)2(2,4-PDC)2, 2,4-PCD = 2,4-pyridinecarboxylate] was synthesized following the previously reported procedure in [11]: 2,4-Pyridinedicarboxlic acid (170 mg, 1.0 mmol) and KOH (2.0 M, 2.0 cm3) in H2O were added to a stirred solution of Mg(NO3)2, (380 mg, 1.5 mmol) in H2O (3 cm3) to give a viscous, opaque, slurry mixture. The reaction mixture was placed inside a Teflon-lined Easy-Prep vessel and heated at 472 K for 35 min in a MARS microwave (CEM Corp.). The reaction temperature was monitored using a fiber-optic sensor. After cooling down to room temperature (30 min), the crystalline solid was purified by short (3 × 20 s) cycles of sonication in fresh H2O, followed by the decanting of the slurry supernatant. Large, colorless prismatic crystals were isolated (average yield: 124 mg). TGA and PXRD were carried out and confirmed the nature of the synthesized material and its purity (see Figures S2 and S3, SM), and the estimated BET surface area of the activated Mg-CUK-1 (100 °C at 1 × 10−4 bar and 2 h).

2.2. Methods

Adsorption Isotherms for CO2. Ultra-pure grade (99.9995%) CO2 gas was purchased from PRAXAIR. CO2 adsorption isotherms at 196 K and up to 1 bar were carried out on a Belsorp mini II analyzer under high vacuum.

Water-loading within Mg-CUK-1. H2O vapor loadings were performed by a dynamic method, using air gas as the carrier gas, and by using a DVS Advantage 1 instrument from Surface Measurement Systems (mass sensitivity: 0.1 mg, relative humidity (RH), accuracy: 0.5% RH, vapor pressure accuracy: 0.7% P/P0). Mg-CUK-1 samples were activated at 100 °C for 1 h under flowing dry N2. The water contents within Mg-CUK-1 analyzed were 25% RH, 22% RH, 20% RH and 18% RH.

Powder X-ray diffraction patterns were collected on a Rigaku Diffractometer, Ultima IV, with a Cu-Kα1 radiation (λ = 1.5406 Å) using a nickel filter. These were obtained from 5° to 50° in 2θ, with 0.02° steps at a 0.08° min−1 scan rate. Profile refinements were performed based on the previously reported Mg-CUK-1-hydrated structure data using the FullProf program (structure NUDLIJ from CCDC database) [14,15].

3. Results

Mg-CUK-1 is assembled from the coordination of Mg(II) metal centers and 2,4-pyridinedicarboxylate ligand. Mg-CUK-1 crystallizes in the space group P21/n and it is constructed around trinuclear [Mg3(μ3-OH)] building blocks (see Figure S1, inset) [11]. Each Mg(II) metal center shows an octahedral coordination environment and links into infinite chains of edge- and vertex-sharing Mg3OH triangles. Mg-CUK-1 shows a 3-D framework structure with diamond-shaped pore dimensions of approximately 8.1 × 10.6 Å (see Figure S1). The estimated BET area (0.005 < P/P0 < 0.15) was equal to 604 m2 g−1, with a corresponding pore volume of 0.22 cm3 g−1.

The water-loading dependence of the porosity of Mg-CUK-1 was analyzed based on the reported [12,13] water adsorption isotherm data. For that purpose, the experimental PXRD patterns were collected at different H2O loadings (see SM, water-loading within Mg-CUK-1, Figure S4) and the cell parameters of the H2O-loaded material (Mg-CUK-1) were determined by the Le Bail methodology (FullProf program; see SM, PXRD profile refinement of Mg-CUK-1, Figures S5–S8) [14,15]. The so-obtained evolution of the cell parameters corroborated the soft crystal properties of Mg-CUK-1: the b-axis increases with the water content from 12.334 to 13.435 Å (see Figure S9). Such a change occurred from the anhydrous form to the eight H2O/UC-loaded versions (Table S1). We indeed observed a dramatic reduction in the accessible space when the H2O concentration increased (see Table 1 and Figure S10).

Table 1

Mg-CUK-1 one-dimensional channel dimensions at different H2O molecule loadings. The window dimensions lb and lc (Å) were estimated using a 0.002 au isosurface with CrystalExplorer [14,15].

Material	H2O/UC	lb (Å)	lc (Å)	OH2O-OH2O (Å)	Pore
Mg-CUK-1	0	6.62	6.51	-	Accessible
Mg-CUK-1···1H2O	1	4.43	6.52	20.5	Accessible
Mg-CUK-1···2H2O	2	4.43	6.52	6.5 or 9.5	Restrained
Mg-CUK-1···4H2O	4	4.68	6.61	4.6 or 6.5	Restrained
Mg-CUK-1···8H2O	8	2.56	6.61	4.6	Non-accessible

The reduction in the minimum channel length is considerably more drastic in the b direction, which can be associated with the position of the hydroxo groups (μ2-OH) that are only present in the b direction of the channel. The minimum channel length in the b direction is reduced from 6.62 Å, in the empty material, to approximately 2.56 Å, with eight water molecules per unit cell, corresponding to more than a 50% reduction in the size of the channel diameter (Table 1). These eight water molecules correspond to one H2O molecule per hydroxo group and, at this point, the inclusion of CO2 is anticipated to not be possible. Since the kinetic diameter of CO2 is 3.3 Å (Figure 1), this essentially inhibits the direct passage of the CO2 molecules through the Mg-CUK-1 network, and therefore results in zero adsorption of CO2.

Figure 1

Crystal structures of Mg-CUK-1 with different H2O molecule loadings, from top to bottom, none, 1, 2, 4 and 8 water molecules per unit cell. (a) View through the a-axis showing the hydrogen-bonded H2O molecules to the hydroxo functional groups (H2O···OH-μ3), and (b) side view of the channel (through the c-axis) and accessible surface, yellow circles represent CO2 kinetic diameter.

4. Discussion

Interestingly, four and two H2O molecules interacting via hydrogen bonding to Mg-CUK-1 (molecules per unit cell) lead to a window reduction of 4.68 and 4.43 Å, respectively (Table 1). However, the minimum distance between two adjacent water molecules is 3.3 and 6.7 Å for Mg-CUK-1 with four and two water molecules, respectively. According to this, the path for the diffusion of CO2 is restrained (Figure 1) and a low CO2 adsorption is expected. Following this trend, an increase in the distance between the water molecules within the pore can result in a favorable space for CO2 to interact with the H2O molecules. When there is one hydrogen-bonded H2O molecule per unit cell, the pore-window is reduced to approximately 4.43 Å and the distance between two water molecules increases to 20.5 Å (Table 1). This can provide enough free space for the CO2 molecules to diffuse within the pore-window and, as we previously reported, a “bottleneck effect’’ occurs [16,17]. This effect is expected to accommodate the CO2 molecules more efficiently, by partially obstructing the pore-windows of Mg-CUK-1. Indeed, this particular configuration (one hydrogen-bonded H2O molecule per unit cell) corresponds to 18% of relative humidity (RH), according to the water adsorption isotherm [12,13]. Remarkably, Mg-CUK-1 revealed a 1.8-fold increase in CO2 capture from 4.6 wt% to 8.5 wt% in the presence of 18% RH [12] (See Figure S11).

5. Conclusions

The structure transformation of Mg-CUK-1 by the incorporation (confinement) of different amounts of water molecules was successfully demonstrated by PXRD (Le Bail methodology refinements). The confinement of one hydrogen-bonded H2O molecule per unit cell (18% RH) produces a bottleneck effect with adequate pore dimensions (4.43 Å) for the proper diffusion of CO2 molecules. Such a structure transformation corroborates a 1.8-fold increase in CO2 capture from 4.6 wt% to 8.5 wt%, as previously reported for Mg-CUK-1 [12].