Anhydrous Proton Conductivity Research Articles

Highly Stable Bismuth-Based Layered Oxides Modified by Phytic Acid for Anhydrous and Water-Assisted Proton Conductivity

Highly Stable Bismuth-Based Layered Oxides Modified by Phytic Acid for Anhydrous and Water-Assisted Proton Conductivity

Convenient Aqueous‐Phase Synthesis of Covalent Organic Frameworks for Anhydrous Proton Conduction

Covalent organic frameworks (COFs) as a kind of emerging materials has been widely concerned. Developing and recovering new COF materials is of great importance for anhydrous proton conduction, most of the synthesis methods are not organic solvent phase or convenient enough, which would inevitably lead to solvent waste and increase environmental burden. Herein, a method of COF synthesis in aqueous phase is developed, which is used for nonpolluting and sustainable fabrication. Benefits from the suitable channels and stability of HCOF‐1, the composite material H3PO4@HCOF‐1 exhibit high proton conductivity (1.29 × 10−4 S cm−1) at 413 K and the crystallinity of HCOF‐1 is maintained well after measurements. This work broadens the scope of COF synthesis and promotes the development of anhydrous proton conduction.

Accelerating Anhydrous Proton Transport in Covalent Organic Frameworks: Pore Chemistry and its Impacts

AbstractProton conduction is important in both fundamental research and technological development. Here we report designed synthesis of crystalline porous covalent organic frameworks as a new platform for high‐rate anhydrous proton conduction. By developing nanochannels with different topologies as proton pathways and loading neat phosphoric acid to construct robust proton carrier networks in the pores, we found that pore topology is crucial for proton conduction. Its effect on increasing proton conductivity is in an exponential mode other than linear fashion, endowing the materials with exceptional proton conductivities exceeding 10−2 S cm−1 over a broad range of temperature and a low activation energy barrier down to 0.24 eV. Remarkably, the pore size controls conduction mechanism, where mesopores promote proton conduction via a fast‐hopping mechanism, while micropores follow a sluggish vehicle process. Notably, decreasing phosphoric acid loading content drastically reduces proton conductivity and greatly increases activation energy barrier, emphasizing the pivotal role of well‐developed proton carrier network in proton transport. These findings and insights unveil a new general and transformative guidance for designing porous framework materials and systems for high‐rate ion conduction, energy storage, and energy conversion.

Accelerating Anhydrous Proton Transport in Covalent Organic Frameworks: Pore Chemistry and its Impacts.

Proton conduction is important in both fundamental research and technological development. Here we report designed synthesis of crystalline porous covalent organic frameworks as a new platform for high-rate anhydrous proton conduction. By developing nanochannels with different topologies as proton pathways and loading neat phosphoric acid to construct robust proton carrier networks in the pores, we found that pore topology is crucial for proton conduction. Its effect on increasing proton conductivity is in an exponential mode other than linear fashion, endowing the materials with exceptional proton conductivities exceeding 10-2 S cm-1 over a broad range of temperature and a low activation energy barrier down to 0.24 eV. Remarkably, the pore size controls conduction mechanism, where mesopores promote proton conduction via a fast-hopping mechanism, while micropores follow a sluggish vehicle process. Notably, decreasing phosphoric acid loading content drastically reduces proton conductivity and greatly increases activation energy barrier, emphasizing the pivotal role of well-developed proton carrier network in proton transport. These findings and insights unveil a new general and transformative guidance for designing porous framework materials and systems for high-rate ion conduction, energy storage, and energy conversion.

Perfluoroalkyl Functionalized Superhydrophobic Covalent Organic Frameworks for Excellent Oil-Water Membrane Separation and Anhydrous Proton Conduction.

Rapid economic development has led to oil pollution and energy shortage. Membrane separation has attracted much attention due to its simplicity and efficiency in oil-water-separation. The development of membrane materials with enhanced separation properties is essential to improve the separation-efficiency. Proton exchange membrane fuel cells (PEMFCs) are expected to replace conventional engines due to their high-power-conversion rates and other favorable properties. Anhydrous-proton-conductingmaterials are vital components of PEMFCs. However, developing stable proton-conducting materials that exhibit high conductivity at varying temperatures remains challenging. Herein, two covalent organic frameworks (COFs) with long-side-chains are synthesized, and their corresponding COF@SSN membranes. Both membranes can effectively separate oil-water mixtures and water-in-oil emulsions. The TFPT-AF membrane achieves a maximum oil-flux of 6.05×105g h-1 m-2 with an oil-water separation efficiency of above 99%, which is almost unchanged after 20 consecutive uses. COF@H3PO4 doped with different ratios of H3PO4 is prepared, the results show that the perfluorocarbon-chain system has excellent anhydrous proton conductivity, achieving an ultra-high proton-conductivityof 3.98×10-1Scm-1 at 125°C. This study lays the foundation for tailor-made-functionalization of COF through pre-engineering and surface-modification, highlighting the great potential of COFs for oil-water separation and anhydrous-proton-conductivity.

Encapsulation of Imidazole into Ce-Modified Mesoporous KIT-6 for High Anhydrous Proton Conductivity.

Imidazole molecules entrapped in porous materials can exhibit high and stable proton conductivity suitable for elevated temperature (>373 K) fuel cell applications. In this study, new anhydrous proton conductors based on imidazole and mesoporous KIT-6 were prepared. To explore the impact of the acidic nature of the porous matrix on proton conduction, a series of KIT-6 materials with varying Si/Al ratios and pure silica materials were synthesized. These materials were additionally modified with cerium atoms to enhance their Brønsted acidity. TPD-NH3 and esterification model reaction confirmed that incorporating aluminum into the silica framework and subsequent modification with cerium atoms generated additional acidic sites. UV-Vis and XPS identified the presence of Ce3+ and Ce4+ in the KIT-6 materials, indicating that high-temperature treatment after cerium introduction may lead to partial cerium incorporation into the framework. EIS studies demonstrated that dispersing imidazole within the KIT-6 matrices resulted in composites showing high proton conductivity over a wide temperature range (300-393 K). The presence of weak acidic centers, particularly Brønsted sites, was found to be beneficial for achieving high conductivity. Cerium-modified composites exhibited conductivity surpassing that of molten imidazole, with the highest conductivity (1.13 × 10-3 S/cm at 393 K) recorded under anhydrous conditions for Ce-KIT-6. Furthermore, all tested composites maintained high stability over multiple heating and cooling cycles.

Exceptional Anhydrous Proton Conduction in Covalent Organic Frameworks.

Covalent organic frameworks (COFs) offer an irreplaceable platform for mass transport, as they provide aligned one-dimensional channels as pathways. Especially, proton conduction is of great scientific interest and technological importance. However, unlike proton conduction under humidity, anhydrous proton conduction remains a challenge, as it requires robust materials and proceeds under harsh conditions. Here, we report exceptional anhydrous proton conduction in stable crystalline porous COFs by integrating neat phosphoric acid into the channels to form extended hydrogen-bonding networks. The phosphoric acid networks in the pores are stabilized by hierarchical multipoint and multichain hydrogen-bonding interactions with the 3D channel walls. We synthesized five hexagonal COFs that possess different pore sizes, which are gradually tuned from micropores to mesopores. Remarkably, mesoporous COFs with a high pore volume exhibit an exceptional anhydrous proton conductivity of 0.31 S cm-1, which marks the highest conductivity among all examples reported for COFs. We observed that the proton conductivity is dependent on the pore volume, pore size, and content of phosphoric acid. Increasing the pore volume improves the proton conductivity in an exponential fashion. Remarkably, changing the pore volume from 0.41 to 1.60 cm3 g-1 increases the proton conductivity by 1150-fold. Interestingly, as the pore size increases, the activation energy barrier of proton conduction decreases in linear mode. The mesopores enable fast proton hopping across the channels, while the micropores follow sluggish vehicle conduction. Experiments on tuning phosphoric acid loading contents revealed that a well-developed hydrogen-bonding phosphoric acid network in the pores is critical for proton conduction.

Novel high temperature proton exchange membranes based on functionalized poly(arylene dimethylamino benzene) polymers

The electrolyte membrane is a critical component in high temperature proton exchange membrane fuel cells (HT-PEMFCs). We have developed a new triarylmethane-backboned polymer, poly(p-triphenyl dimethylamino benzene) (PTDB), by using p-triphenyl and 4-(dimethylamino)benzaldehyde as monomers through a one-step straightforward Friedel-Crafts reaction. The presence of tertiary amine groups in PTDB enables strong interaction with phosphoric acid (PA) molecules. To improve PA doping content and proton conductivity, both copolymers containing biphenyl repeat unite and side-chain quaternized polymers are synthesized. Results show that the 3-bromopropyl trimethylammonium bromide grafted membrane (PTDB-QA) outperforms the poly(triphenyl-biphenyl-dimethylamino benzaldehyde) (P(Tx%-By%-DB)) copolymer membranes. After being doped in an 85 wt% PA solution at 80 °C, the PTDB-QA membrane exhibits a PA uptake of 160%, resulting in an anhydrous proton conductivity of 0.054 S cm−1 at 180 °C and mechanical strength of 10.1 MPa at room temperature. Under the H2-air condition without any back pressure, the peak power density of a single cell based on PTDB-QA/160%PA reaches 230 mW cm−2 at 160 °C. This work presents a promising new membrane for HT-PEMFC applications.

Sulfonated poly(ether ether ketone)-Protic ionic Liquid-Based anhydrous Proton-Conducting composite polymer electrolyte membranes for High-Temperature fuel cell applications

A high-temperature polymer electrolyte membrane fuel cell (PEMFC) has enormous potential to produce clean energy with minimal environmental pollution along with high energy density and conversion efficiency. In the present work, anhydrous proton-conducting polymer electrolyte membranes for prospective high-temperature fuel cell application were successfully prepared using different protic ionic liquids (PILs) and sulfonated poly(ether ether ketone) (SPEEK). The protic ionic liquids (PILs), 2-hydroxyethylammonium formate, diethylmethyl ammonium triflate, 1-ethylimidazolium bis(trifluoromethylsulfonyl)imide, 1,2-dimethyl imidazolium bis(trifluoro methylsulfonyl)imide, and diethylmethylammonium methanesulfonate were selected based on their favorable physicochemical properties. The effect of the incorporation of the PIL on the structural, thermal, and electrical transport properties of the composite SPEEK polymer electrolyte membranes was studied. The prepared polymer electrolyte membranes (PEMs) were characterized using Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffractometry (XRD), and electrochemical impedance spectroscopy (EIS) techniques. FTIR results indicated an interaction between the PIL and the SPEEK, which resulted in homogeneous and flexible membranes. The DSC results confirmed good miscibility and elucidated plasticizing effect of the incorporated PIL on the SPEEK polymer matrix. All the PEMs showed good thermal stability and high-temperature anhydrous proton conductivity, achieving best proton conductivity, ≈8 × 10–3 S cm−1 at 120 °C and low activation energy ≈0.26 eV, making it suitable for prospective high-temperature PEMFC applications.

Covalently crosslinked poly(biphenyl dimethylamino benzene) membranes for high temperature proton exchange membrane fuel cells

The electrolyte membrane plays a pivotal role in high temperature proton exchange membrane fuel cells (HT-PEMFCs). Herein, we develops a new triarylmethane-backboned polymer, poly (biphenyl dimethylamino benzene) (PBDAB), synthesized through a facile one-step Friedel-Crafts reaction using biphenyl and 4-(dimethylamino) benzaldehyde as monomers. The presence of tertiary amine groups in PBDAB facilitates strong interactions with phosphoric acid (PA) molecules. To enhance the membrane's dimensional and mechanical stabilities, covalent crosslinking is performed via the Menshutkin reaction between the tertiary amine groups in PBDAB and chloromethyl groups in various crosslinkers. In order to study the influence of crosslinker chemical structure on the properties of PBDAB-based membranes, five different crosslinkers are employed, including small-molecule types such as 1,2-bis(2-chloroethoxy) ethane (BCE) and 1,4-bis(chloromethyl) benzene (BCB), siloxane type 3-chloropropyl (trimethoxy) silane (CTS), polymer types such as poly (vinylbenzyl chloride) (PVBC) and polyepichlorohydrin (PECH). Results reveal that the flexible and ether containing polymer crosslinker of PECH crosslinked membrane, denoted as CL-y%PECH, exhibits superior overall performance. When doped in an 85 wt% PA solution, the CL-5%PECH membrane achieves a PA uptake of 201%, resulting in an anhydrous proton conductivity of 0.064 S cm−1 at 180 °C and a mechanical strength of 7.2 MPa at room temperature. Using H2 and O2 as fed gases without humidification and backpressure, a single cell with abovementioned membrane attains a peak power density of 302 mW cm−2 at 160 °C. This work offers a kind of promising PBDAB based membranes for HT-PEMFC applications.

Improving the ohmic polarization of high-temperature proton exchange membrane fuel cells using crosslinked polybenzimidazole membranes containing acidophilic quaternary ammonium groups synthesized by one-step strategy

Ingenious crosslinked network structure in phosphoric-acid-doped polybenzimidazole membranes can mitigate the mutual restriction of proton conductivity and mechanical properties. However, the complicated synthesis of tailored macromolecular crosslinker and the time-consuming post-treatment hinder their practical application as high-temperature proton exchange membranes. Herein, crosslinked polybenzimidazole membranes are synthesized using small molecular crosslinkers containing acidophilic quaternary ammonium groups through a one-step crosslinking strategy. After doping with phosphoric acid, the quaternary ammonium-biphosphate ion-pair coordination and the crosslinked structure result in the improved anhydrous proton conductivity, oxidation stability, and mechanical strength of the formed membranes compared to the sample without the crosslinking structure. A membrane with the optimized degree of crosslinking exhibits an anhydrous conductivity of 72.27 mS/cm at 160 °C, with a tensile strength of 12.14 MPa. Benefiting from the crosslinked structure and high proton conductivity, the accordingly formed membrane electrode assembly possesses a high open-circuit voltage of 1.01 V and animproved ohmic polarization, delivering a peak power density of 0.66 W/cm2 using hydrogen as fuel and air as oxidant.

Grafting of Amine End-Functionalized Side-Chain Polybenzimidazole Acid-Base Membrane with Enhanced Phosphoric Acid Retention Ability for High-Temperature Proton Exchange Membrane Fuel Cells.

A high phosphoric acid uptake and retention capacity are crucial for the high performance and stable operation of phosphoric acid/polybenzimidazole (PA/PBI)-based high-temperature proton exchange membranes. In this work, amine end-functionalized side-chain grafted PBI (AGPBI) with different grafting degrees are synthesized to enhance both the phosphoric acid uptake and the acid retention ability of the accordingly formed membranes. The optimized acid-base membrane exhibits a PA uptake of 374.4% and an anhydrous proton conductivity of 0.067 S cm-1 at 160 °C, with the remaining proton conductivity percentages of 91.0% after a 100 h stability test. The accordingly fabricated membrane electrode assembly deliver peak power densities of 0.407 and 0.638 W cm-2 under backpressure of 0 and 200 kPa, which are significantly higher than 0.305 and 0.477 W cm-2 for the phosphoric acid-doped unmodified PBI membrane under the same conditions.

High anhydrous proton conductivity and a smart proton transportation approach of a sulfate coordination polymer.

We successfully synthesized a one-dimensional cobalt sulfate coordinating polymer, whose simple hydrogen bond web structure facilitated the analysis of the proton transfer process. At 175 °C, without humidity, the conductivity is 0.0311 S cm-1, which exceeds those of most of the organic inorganic hybrid materials under anhydrous conditions (world record rank 8). Based on its crystal structure and theoretical calculations, the subversive proton conduction pathway was inferred clearly. We, for the first time, found that the proton smartly chose the path with a lower energy barrier but not the one with short distance to transport avoiding short circuit.

Construction of Zr-Metal-Organic Frameworks-Based Composite Materials toward Anhydrous Proton Conduction and Photocatalytic CO2 Reduction.

Metal-organic frameworks constructed from Zr usually possess excellent chemical and physical stability. Therefore, they have become attractive platforms in various fields. In this work, two families of hybrid materials based on ZrSQU have been designed and synthesized, named Im@ZrSQU and Cu@ZrSQU, respectively. Im@ZrSQU was prepared through the impregnation method and employed for proton conduction. Im@ZrSQU exhibited terrific proton conduction performance in an anhydrous environment, with the highest proton conduction value of 3.6 × 10-2 S cm-1 at 110 °C. In addition, Cu@ZrSQU was synthesized via the photoinduction method for the photoreduction of CO2, which successfully promoted the conversion of CO2 into CO and achieved the CO generation rate of up to 12.4 μmol g-1 h-1. The photocatalytic performance of Cu@ZrSQU is derived from the synergistic effect of Cu NPs and ZrSQU. Based on an in-depth study and discussion toward ZrSQU, we provide a versatile platform with applications in the field of proton conduction and photocatalysis, which will guide researchers in their further studies.

Ionization of a neutral MOF to disperse and anchor acid for boosting anhydrous proton conductivity

Although incorporation of proton conducting molecules (PCMs) is one of the most effective methods to enhance the anhydrous conductivity, most materials including MOFs are challenged by the leakage and poor dispersion of PCMs, severely decreasing the anhydrous proton conductivity. Herein, we propose a neutral framework ionization strategy to construct positive and negative charge centers for dispersing and anchoring the encapsulated PCMs. The N+ and –SO3– sites in MOF-867-PS are thus constructed through modifying MOF-867 with 1,3-propane sultone (PS). After incorporating trifluoromethanesulfonic acid (CF3SO3H, TFOH) the resultant MOF-867-PS-XTFOH (X is volume of TFOH/μL per 100 mg MOFs) composites disperse and anchor the CF3SO3− and H+ ions through electrostatic interaction to form smooth proton transport pathway, benefiting to the high proton conductivity. Especially, MOF-867-PS-100TFOH exhibits sharply enhanced proton conductivity over 10−3 S cm−1, almost two orders of magnitude higher than pristine MOF-867 loaded with equimolar acid and comparable to the top-ranking anhydrous proton conducting MOF composites. This work is the first post–synthetic modification in MOFs to assemble multiple sites for anchoring the functional molecules, opening an effective path to fabricate the high–performance MOFs for proton conduction or other functionalities.

Linkage conversions in single-crystalline covalent organic frameworks.

Single-crystal X-ray diffraction is a powerful characterization technique that enables the determination of atomic arrangements in crystalline materials. Growing or retaining large single crystals amenable to it has, however, remained challenging with covalent organic frameworks (COFs), especially suffering from post-synthetic modifications. Here we show the synthesis of a flexible COF with interpenetrated qtz topology by polymerization of tetra(phenyl)bimesityl-based tetraaldehyde and tetraamine building blocks. The material is shown to be flexible through its large, anisotropic positive thermal expansion along the c axis (αc = +491 × 10-6 K-1), as well as through a structural transformation on the removal of solvent molecules from its pores. The as-synthesized and desolvated materials undergo single-crystal-to-single-crystal transformation by reduction and oxidation of its imine linkages to amine and amide ones, respectively. These redox-induced linkage conversions endow the resulting COFs with improved stability towards strong acid; loading of phosphoric acid leads to anhydrous proton conductivity up to ca. 6.0 × 10-2 S cm-1.

Expanding the dimensionality of proton conduction enables ultrahigh anhydrous proton conductivity of phosphoric acid-doped covalent-organic frameworks

Expanding the dimensionality of proton conduction enables ultrahigh anhydrous proton conductivity of phosphoric acid-doped covalent-organic frameworks

Molecular Complexation of Polymers and Metal Oxide Clusters for Semicrystalline, Thermoplastic Anhydrous Proton Exchange Membranes in Fuel Cells.

With the manipulation of surface charges and loadings, 1 nm super-acidic metal oxide clusters can co-crystallize with poly(ethylene glycol) (PEG) at molecular scale for thermoplastic anhydrous proton exchange membranes (PEMs). The coexistence of crystalline and amorphous regions endows the PEMs with a high Young's modulus and high flexibility, while the noncovalent complex interactions enable facile preparation and (re)processing. Furthermore, the diffusive dynamics of PEG chains is slowed by the confinement effect, while the local segmental dynamics is accelerated due to the transition of the chain conformation from helix to zigzag when confined in the crystalline framework. This greatly facilitates proton transportation in the crystalline region for an excellent anhydrous proton conductivity of 4.5 × 10-3 S cm-1 at 90 °C. The balanced proton conductivity, mechanical strength, and processability of the PEMs contribute to the promising power density of H2/O2 fuel cells assembled with co-crystalline PEMs at high temperatures under dry conditions.

Modulation of defects in metal organic gels to enhance anhydrous proton conduction from subzero to moderate temperature

Exploitation of solid-state proton-conducting materials with high anhydrous proton conductivity from subzero temperature (<273 K) to moderate temperature (>353 K) is a great challenge. Here, Brönsted acid-dopped zirconium-organic xerogels (Zr/BTC-xerogels) are prepared for anhydrous proton conduction from subzero to moderate temperature. Abundant acid sites and strong H-bonding interactions make the CF3SO3H (TMSA)-introduced xerogel gain high proton conductivity from 9.0 × 10-4 S cm−1 (253 K) to 1.40 × 10-2 S cm−1 (363 K) under anhydrous conditions, which are in the leading level. This provides a new possibility to develop wide-operating-temperature conductors.

Columnar Liquid Crystals of Copper(I) Complexes with Ionic Conductivity and Solid State Emission.

Two neutral copper(I) halide complexes ([Cu(BTU)2X], X = Cl, Br) were prepared by the reduction of the corresponding copper(II) halides (chloride or bromide) with a benzoylthiourea (BTU, N-(3,4-diheptyloxybenzoyl)-N'-(4-heptadecafluorooctylphenyl)thiourea) ligand in ethanol. The two copper(I) complexes show a very interesting combination of 2D supramolecular structures, liquid crystalline, emission, and 1D ionic conduction properties. Their chemical structure was ascribed based on ESI-MS, elemental analysis, IR, and NMR spectroscopies (1H and 13C), while the mesomorphic behavior was analyzed through a combination of differential scanning calorimetry (DSC), polarizing optical microscopy (POM), and powder X-ray diffraction (XRD). These new copper(I) complexes have mesomorphic properties and exhibit a hexagonal columnar mesophase over a large temperature range, more than 100 K, as evidenced by DSC studies and POM observations. The thermogravimetric analysis (TG) indicated a very good thermal stability of these samples up to the isotropization temperatures and over the whole temperature range of the liquid crystalline phase existence. Both complexes displayed a solid-state emission with quantum yields up to 8% at ambient temperature. The electrical properties of the new metallomesogens were investigated by variable temperature dielectric spectroscopy over the entire temperature range of the liquid crystalline phase. It was found that the liquid crystal phases favoured anhydrous proton conduction provided by the hydrogen-bonding networks formed by the NH…X moieties (X = halide or oxygen) of the benzoylthiourea ligand in the copper(I) complexes. A proton conductivity of 2.97 × 10-7 S·cm-1 was achieved at 430 K for the chloro-complex and 1.37 × 10-6 S·cm-1 at 440K for the related bromo-complex.