Rapid Diffusion Research Articles

Fabrication of thick Cr masks for reactive ion substrate etching by electron beam lithography and lift-off techniques

Fabrication of tall Cr nanostructures of different shapes by lithography and lift-off processes is demonstrated. By varying resist thickness, metal layer thickness, and diameter of holes in the resist mask, it is demonstrated that metal structures with shapes ranging from sharp-tipped conical over flat-top cones to nearly cylindrical can be fabricated. A comparison of resist layer dissolution in acetone, covered by Ag and Cr films, reveals that Cr films grow with an open structure of particles that allow rapid solvent diffusion through Cr layers that are several hundred nanometers thick. On the other hand, the 2D growth of Ag on the resist forms a barrier against acetone diffusion. The open structure of Cr enables the lift-off process to fabricate several-μm-high nanostructures using a single resist layer. As an example, high-aspect-ratio Si structures are demonstrated by reactive ion etching using thick Cr layers as a mask, fabricating nanopillars with 3 μm height at room temperature.

Tailoring Zn2+ Flux by an Ion Acceleration Layer Modified Separator for High-Rate Long-Lasting Zn Metal Anodes.

A large concentration gradient originating from sluggish ion transport on the surface of Zn metal anodes will result in uneven Zn2+ flux, giving rise to severe dendrite growth, especially at high current density. Herein, an ion acceleration layer is introduced by a facile separator engineering strategy to realize modulated Zn2+ flux and dendrite-free deposition. Zinc hexacyanoferrate as the modifying agent featuring strong zincophilicity and rapid diffusion tunnel can enable fast trap for Zn2+ near the electrode surface and immediate transport onto deposition sites, respectively. The ion acceleration effect is substantiated by improved ion conductivity, decreased activated energy, and promoted Zn2+ transference number, which can moderate concentration gradient to guide homogenous Zn2+ flux distribution. As a result, the separator engineering guarantees Zn||Zn symmetrical cells with long-term stability of 2700 h at 2 mA cm-2, and 1770 h at a large current density of 10 mA cm-2. Moreover, cycling stability and rate capability for full cells with different cathodes can be substantially promoted by the modified separator, validating its superior practical feasibility. This study supplies a new scalable approach to tailoring ion flux near the electrode surface to enable robust Zn metal anodes at a high current density.

The public use of early-stage scientific advances in carbon dioxide removal: a science-technology-policy-media perspective

Abstract While Carbon Dioxide Removal (CDR) solutions are considered essential to meet Paris Agreement objectives and curb climate change, their maturity and current ability to operate at scale are highly debated. The rapid development, deployment, and diffusion of such methods will likely require the coordination of science, technology, policy, and societal support. This article proposes a bibliometric approach to quantify the public use of early-stage research in CDR. Specifically, we employ generalized linear models to estimate the likelihood that scientific advances in eight different carbon removal solutions may induce (i) further production of scientific knowledge, (ii) technological innovation, and (iii) policy and media discussion. Our main result is that research in CDR is of significant social value. CDR research generates significant, positive, yet heterogeneous spillovers within science and from science to technology, policy, and media. In particular, advances in Direct Air Capture spur further research and tend to result in patentable technologies, while Blue Carbon and Bio-energy with Carbon Capture and Storage appear to gain relative momentum in the policy and public debate. Moreover, scientific production and collaborations cluster geographically by type of CDR, potentially affecting long-term carbon removal strategies. Overall, our results suggest the existence of coordination gaps between science, technology, policy, and public support.

β-galactosidase instructed in situ self-assembly fluorogenic probe for prolonged and accurate imaging of ovarian tumor

Fluorescent probes are essential for optical imaging and have been extensively employed for precise cancer diagnosis studies. β-galactosidase (β-gal) serves as a primary biomarker for ovarian cancer and has been utilized to develop imaging probes for accurate tumor diagnosis. However, traditional small molecular probes have limitations in terms of rapid diffusion and metabolic clearance from the target lesion, resulting in a short imaging window and compromised tumor-to-background ratios (TBR). Herein, we integrated an enzyme-instructed in situ self-assembly strategy to construct Gal-IRFF, a small molecule-based activatable near-infrared (NIR) fluorogenic probe. Upon cleavage by endogenous β-gal overexpressed in ovarian cancer cells, IRFF exhibited enhanced NIR fluorescence signals and self-assembled into nanoparticles through intermolecular interactions of the Phe-Phe (FF) dipeptide moiety, which facilitated probe accumulation and retention within the tumor lesion. Compared with the small molecule probe Gal-IR, our proposed self-assembly probe Gal-IRFF demonstrated a lower limit of detection (LOD) towards β-gal and showed remarkable improvements in distribution and retention time within SKOV3 cells in vitro and tumors in vivo, thereby providing a long-term imaging window for real-time monitoring β-gal levels in ovarian tumors. Therefore, this study highlights the potential of an enzyme-instructed self-assembly fluorogenic probe design approach for achieving precise tumor diagnosis in vivo.

Enhanced corrosion resistance of NbTaMoW medium entropy alloy coatings in simulated PEMFC environments: Experimental and computational insights

An anti-corrosive and conductive NbTaMoW medium entropy alloy (MEA) coating was deposited on 304 stainless steel using a dual-cathode glow discharge technology. This MEA coating exhibits a single body-centered cubic phase with about 10 nm grains, and forms a passivation film with significantly enhanced corrosion resistance at any given HF concentration. The lower adsorption energy of Nb atoms for oxygen atoms leads to the enrichment of Nb oxides in the passivation film, which is beneficial for hindering the rapid diffusion of F− ions. These findings underscore the potential of NbTaMoW MEA coatings to improve the durability and efficiency of PEMFCs.

New insight on the formation of uneven oxide scales on AFA steel in supercritical CO2: Roles of recrystallization degree on the high temperature corrosion resistance

Uneven oxide scale is a common phenomenon in high-temperature corrosion, but the formation mechanism has not been fully uncovered. A new alumina-forming austenitic (AFA) stainless steel with superior corrosion resistance in 650°C/15MPa SC-CO2, has been systematically investigated. It is demonstrated that the uneven oxide was formed by the significant impact of the recrystallization behavior of AFA steel on its microstructural evolution and subsequent corrosion behavior. Compared with the thin oxide scale, the thick oxide scale was caused by the relatively higher density of dislocations and grain boundaries of matrix resulting from delayed recrystallization, which facilitated the rapid outward diffusion of ions.

Co-doped Ni-PBA anchored on optimized ZIF-67-derived Co/N-doped hollow carbon framework for high-performance hybrid capacitive deionization

Prussian blue analogues (PBAs) are considered to be a promising electrode material for hybrid capacitive deionization (HCDI) due to their open lattice structure, adjustable composition and high theoretical capacity. Nevertheless, the performance of PBAs in practical applications is limited by their low intrinsic conductivity and structural degradation. Herein, we demonstrate an advanced heterostructure CoNi-PBA@Co/N-HC by anchoring cobalt-doped nickel hexacyanoferrate (CoNi-PBA) on cobalt/nitrogen-doped hollow porous carbon (Co/N-HC) derived from cobalt-based metal–organic frameworks (ZIF-67). Co/N-HC as the conductive growth framework of CoNi-PBA can not only promote the rapid charge transfer and efficient ion diffusion, but also mitigate the structural degradation of CoNi-PBA crystals during ion intercalation/deintercalation. Moreover, the doped Co in CoNi-PBA is derived from Co/N-HC, allowing the heterostructures to form more stable and tighter interconnections. Therefore, the optimal PBA@Co/N-HC300 electrode exhibits reduced equivalent series resistance (Rs 1.10 Ω < Rs (PBA) 1.41 Ω), enhanced ion diffusion rate (DNa+ 2.86 × 10−16 > DNa+(PBA) 4.65 × 10−18) and exceptional electrochemical stability (99 % capacitance retention, 500 times CV tests). Correspondingly, the HCDI cell PBA@Co/N-HC300//Co/N-HC demonstrates good Na+ removal capacity (33.37 mg·g−1), excellent charge efficiency (83.65 %), diminished energy consumption (0.657 kWh kg−1-NaCl) and improved cycle stability (90.8 % capacity retention, 40 cycles).

Understanding the impact of porosity on Li-ion diffusion enhancement in micro-sized silicon particles for advanced batteries

Lithium-ion batteries (LIBs) require advanced and practical anode materials, such as porous silicon (PSi), which can meet these expectations due to their rapid Li-ion diffusion rates and structural relaxation. Several studies have focused on the structural design of PSi or its composites to improve Li-ion diffusion; however, no systematic and quantitative evaluations of the impact of porosity on Li-ion diffusion and battery performance have been reported. Therefore, to understand the impact of porosity on Li-ion diffusion, we developed micro-sized porous silicon (m-PSi) particles with various porosities via metal-assisted chemical etching (MACE) method using different concentrations of AgNO3 (0.02–0.08 M). Among the as-prepared samples, m-PSi-0.06 (prepared using 0.06 M AgNO3) with ∼70 % porosity achieved a maximum Li-ion diffusion rate of 2.35 × 10−9 cm2 s−1. This led to a high-rate capability, enhanced Li-ion storage, and better cyclic retention of 61.4 % compared to the non-porous micro-sized Si (m-Si) (5.8 %) sample at a current density of 0.1 A g−1. Furthermore, the optimal porosity of m-PSi-0.06 resulted in an impressive rate capability of 760 mAh g−1 at a high current density of 4 A g−1 with a recovery rate of 80 %. The improved efficiency of m-PSi-0.06 is attributed to its optimized mesoporosity, which ensures sufficient space for Li-ion storage and shortens the effective transmission path to accelerate Li-ion diffusion. Moreover, the mesopores provide a greater number of active sites for the reversible adsorption of Li ions, thereby improving the capacitive behavior of the anode. In contrast, the highly nanoporous m-PSi-0.08, with a pore diameter of 1–3 nm, impeded Li-ion movement and restricted diffusion. These results reveal that a high nano porosity hinders Li-ion diffusion, whereas an optimal mesoporosity ensures swift diffusion in m-PSi anodes. These insights could guide the design of Si-based anode materials for advanced LIBs.

Strong adsorption Fe[sbnd]N[sbnd]C catalytic cathode for 50,000 cycles aqueous zinc-iodine batteries

Aqueous zinc-iodine batteries have garnered increasing attention due to their low cost and high safety. However, their practical application is impeded by sluggish iodine redox reaction kinetics and the “shuttle effect” of polyiodides, which result in poor rate performance and limited cycled life. Here, we developed N-doped porous carbon fiber derived from Prussian blue and polyacrylonitrile (PAN) as a self-supporting cathode material for zinc-iodine batteries. The material demonstrates a high iodine adsorption capacity in the electrolyte solution. Density Function Theory (DFT) calculations indicate that the prepared materials demonstrate good catalytic activity. Furthermore, the interconnected carbon fiber network, characterized by high conductivity and a large specific surface area, facilitates rapid electron transport and ion diffusion. Consequently, the zinc-iodine battery demonstrates outstanding rate performance (148mAh g−1 at a high current density of 10 A/g) and a long cycling life of 50,000 cycles, with a capacity retention rate of 72.1 %. Additionally, the battery achieves an impressive calendar life of 8 months and 23 days.

Coating flow of a liquid film with colloidal particles on a vertical fiber

A thin liquid film of colloidal suspension is considered which is spreading down on a vertical cylinder under the effect of gravity. A precursor film model is employed at the three-phase contact line to relieve the stress singularity. The curvature pressure leads to the formation of a capillary ridge at the contact-line. Bulk and surface colloids are assumed to be present in the liquid film. The interfacial pattern is governed by the film evolution equation, obtained by simplifying mass and momentum balance equations within the lubrication assumption, while rapid vertical diffusion is assumed for the advection–diffusion equation of the bulk concentration. Fluid viscosity and diffusivity are considered to be functions of the particle volume fraction. The effects of the bulk and surface colloids on the spreading film dynamics are systematically studied. The presence of bulk colloids leads to the thinning of the capillary ridge for smaller inlet bulk colloid concentrations. On the other hand, a larger inlet bulk concentration leads to the formation of a secondary advancing front behind the capillary ridge in the film profile. A reduced contact point velocity is observed with an increase in the upstream bulk concentration. Surface concentration is found to result in a hump-like structure behind the capillary ridge in the upstream direction due to solutal Marangoni stress. The Marangoni stress also hinders the surface-tension-driven spreading, resulting in a smaller contact line velocity. Reducing the Bond number results in unstable film profiles, which lead to a wave-like structure in the region with no bulk concentration gradients.

Construction of VO2@V2C MXene heterostructure toward superior-rate rechargeable aqueous zinc batteries

V2C MXene delivers excellent metallic properties and robust mechanical stability. However, its low capacity, easy volume expansion during charge/discharge and relatively short cycle life limits its further development. It is an effective strategy to build Van der Waals heterostructures that can shield the monolithic materials from defects and integrate the advantages of the monolithic materials. Herein, via a one-step hydrothermal method, a VO2@V2C heterostructure is successfully constructed by the controllable oxidation of V2C, which allows for shorter ion diffusion distances, faster ion transport and enhancement of hydrophilic properties of the material. The VO2@V2C heterostructures have incredible reversibility (440.9 mAh/g at 0.2 A/g), remarkable cycling stability (142.7 mAh/g at 1.0 A/g after 900 cycles) and superior-rate capacity (255.3 mAh/g at 6.0 A/g). Density functional theory (DFT) calculations revealed that VO2@V2C possesses excellent adsorption capacity for zinc ions and outstanding electrical conductivity. The heterogeneous interface between the two materials is conducive to the increase of the embedding sites of zinc ions, which promotes the homogeneous distribution and rapid diffusion of zinc ions in the materials, and consequently enhances the capacity and cycling reliability of the electrodes. It provides a new idea for the selection of cathode electrodes for aqueous zinc ion batteries (ZIBs) in present study.

Insight into the oxidation behavior and excellent internal oxidation and nitridation resistance of Fe71.5-x(Ni, Cr, Ti)28.5Alx complex concentrated alloys by advanced characterization

For precipitate-strengthened alloys, the decomposition of the precipitates at the subsurface during high-temperature oxidation is detrimental to mechanical properties. In this study, we adjusted Al concentrations in Fe71.5-x(Ni, Cr, Ti)28.5Alx (x = 8, 12, and 16 at. %) complex concentrated alloys (CCAs) to precipitate elongated cuboidal L21 with higher density and Al concentration, as well as reduced inter-precipitate spacing. This is more conducive to the rapid diffusion of Al to the matrix and grain boundaries, promoting the formation of a continuous and compact Al2O3 layer with random crystallographic orientation at 800 °C in air. This not only inhibits the further decomposition of the L21 phase but also avoids internal oxidation and nitridation.

Zwitterion Intercalated Manganese Dioxide Nanosheets as High-Performance Cathode Materials for Aqueous Zinc Ion Batteries.

In this study, a novel approach is introduced to address the challenges associated with structural instability and sluggish reaction kinetics of δ-MnO2 in aqueous zinc ion batteries. By leveraging zwitterionic betaine (Bet) for intercalation, a departure from traditional cation intercalation methods, Bet-intercalated MnO2 (MnO2-Bet) is synthesized. The positively charged quaternary ammonium groups in Bet form strong electrostatic interactions with the negatively charged oxygen atoms in the δ-MnO2 layers, enhancing structural stability and preventing layer collapse. Concurrently, the negatively charged carboxylate groups in Bet facilitate the rapid diffusion of H+/Zn2+ ions through their interactions, thus improving reaction kinetics. The resulting MnO2-Bet cathode demonstrates high specific capacity, excellent rate capability, fast reaction kinetics, and extended cycle life. This dual-function intercalation strategy significantly optimizes the electrochemical performance of δ-MnO2, establishing it as a promising cathode material for advanced aqueous zinc ion batteries.

Adsorption of fluoxetine in aqueous environments: Development of macroporous cryogels based on sodium poly(acrylate) and carboxymethyl chitosan

This study focuses on the development of macroporous monoliths using cryopolymerization of sodium acrylate/carboxymethyl chitosan solutions for the adsorption of the antidepressant fluoxetine in aqueous environments. The cryogels were characterized using various analytical techniques, and the effects of pH, temperature, initial concentration, and contact time on the adsorption capacity were investigated. The surface charge of the cryogel was negative when pHsolution > pHPZC, and pH 8.5 was optimal for swelling rates and fluoxetine removal efficiency. The NaPA4-CMCs cryogel (0.5 mg.mL−1) showed the best adsorption performance, with the pseudo-first-order model best describing the experimental kinetics data. The intraparticle diffusion model revealed rapid diffusion through macropores and mesopores. The Langmuir model fitted well to the experimental adsorption equilibrium data, with qmax = 80.6 ± 3.4 mg.g−1. The adsorption process was favorable, exothermic, and governed by physisorption, involving electrostatic, hydrogen bonding, π–π, and hydrophobic interactions. The binary solvent HCl (0.1 M)/methanol 1:1 v/v was effective for regenerating the adsorbent, with adsorption efficiency greater than 60 % after three cycles of reuse. The study highlights the potential of these macroporous monoliths for the effective removal of antidepressants from aqueous environments.

Development of metal oxide Nanocomposite-Coated electrospun nanofibers for highly sensitive xanthine monitoring

Developing a durable, cost-effective, and readily available electroactive sensor that doesn’t depend on noble metals is crucial for the selective and sensitive monitoring of xanthine (Xn) to overcome the risks linked to metabolic disorders like gout, xanthinuria, and renal failure. Thus, to meet these requirements, herein we have designed a noble-metal-free highly sensitive and selective electrochemical sensor for Xn. We have developed an electrochemical sensor by depositing Co3O4-NiO nanoblossoms on the surface of cellulose acetate (CA) and polyaniline (PANI) based electrospun nanofibers. These electrospun nanofibers facilitate rapid diffusion of Xn molecules to the sensing interface via amine and imine groups, leading to fast response by providing a smooth pathway for transportation of electrons. Moreover, synergistic characteristics of CNNB with electrospun nanofibers contribute to the selective binding of Xn with quick response as well. Our findings reveal that fabricated material exhibits high sensitivity (5 μA μM−1), a response range (0.1–42 µM) with remarkably low limit of detection (0.03 µM). Additionally, our designed electrode demonstrates more selectivity towards Xn in the presence of other interfering species. The designed electrochemical sensor has shown greater reliability in terms of reproducibility and reusability with robust response in human serum samples.

High-Performance Polyimide Covalent Organic Frameworks for Lithium-Ion Batteries: Exceptional Stability and Capacity Retention at High Current Densities.

Organic polymers are considered promising candidates for next-generation green electrode materials in lithium-ion batteries (LIBs). However, achieving long cycling stability and capacity retention at high current densities remains a significant challenge due to weak structural stability and low conductivity. In this study, we report the synthesis of two novel polyimide covalent organic frameworks (PI-COFs), COF-JLU85 and COF-JLU86, by combining truxenone-based triamine and linear acid anhydride through polymerization. These PI-COFs feature layers with pore channels embedded with 18 carbonyl groups, facilitating rapid lithium-ion diffusion and enhancing structural stability under high current densities. Compared to previously reported organic polymer materials, COF-JLU86 demonstrates the excellent performance at high current densities, with an impressive specific capacity of 1161.1 mA h g-1 at 0.1 A g-1, and outstanding cycling stability, retaining 1289.8 mA h g at 2 A g-1 after 1500 cycles and 401.1 mA h g-1 at 15 A g-1 after 10000 cycles. Additionally, in-situ infrared spectroscopy and density functional theory (DFT) calculations provide mechanistic insights, revealing that the high concentration of carbonyl redox-active sites and the optimized electronic structure contribute to the excellent electrochemical performance.

A general methodology for the in situ construction of MxSy@N,S-C composites from L-cysteine for sodium-ion battery applications

High-capacity metal sulfides have been extensively investigated as cathode materials for secondary batteries. Despite their high capacity, the redox potential of metal sulfides is limited to 2.7 V. Therefore, researchers explored its application as a negative electrode material and discovered its exceptional electrochemical performance. However, the conventional methods for synthesizing transition metal sulfides (TMS) inevitably require an external source of sulfur for secondary sulfidation, resulting in energy dissipation. In this study, L-cystine was adopted as a polydentate ligand for the synthesis of MxSy@N, SC metal-organic frameworks, which can confine the desired carbon, nitrogen, and sulfur sources within the framework. This approach facilitates one-step sintering to obtain nitrogen-doped transition metal sulfides. The structure composition and electrochemical reaction mechanism of FeS@N,S-C as the negative electrode in Na-ion batteries were studied through scanning electron microscopy (SEM)/transmission electron microscopy (TEM) and X-ray diffraction (XRD)/X-ray photoelectron spectroscopy (XPS) analysis. The electrochemical properties of FeS@N,S-C materials were test as an example. The FeS@N, SC composite exhibited a reversible Na+ storage capacity of 724.4 mAh g−1 at a current density of 200 mA g−1, and still maintained a reversible capacity of 600.7 mAh g−1 at a current density of 2000 mA g−1, demonstrating excellent rate performance. After 200 cycles, the material was still able to retain 97.3 % of the discharge specific capacity, demonstrating fine cycle performance. It shows that the FeS@N, SC composite has rapid electron conduction ability and high sodium ion diffusion coefficient. At the same time, a rapidly charge-discharge process can be achieved with a large capacitive contribution, indicating the great potential of this material as a sodium-ion battery.

Molecular Design of Solid Polymer Electrolytes with Enthalpy-Entropy Manipulation for Li Metal Batteries with Aggressive Cathode Chemistry.

Solid polymer electrolytes (SPEs) with high ion conductivity, high Li+ transference number, and a wide electrochemical window are promising for the next-generation high-energy Li metal batteries (LMBs). Here we describe an enthalpy-entropy manipulation strategy enabling a class of polycarbonate-based copolymeric electrolytes (PCCEs) with regulated cation/anion solvation via a molecular design of the polymer backbone. By integrating a weakly solvating linear carbonate with another strongly solvating cyclic carbonate segment in the polymer backbone, the cation-dipole coordination for Li+ ions (with two types of carbonyl groups) is weakened (low enthalpy penalty) and nondirectional (high entropy penalty), which enables a weak solvation and rapid diffusion of Li+. We further introduce a bis-acrylamide-based cross-linking segment which, other than imparting high mechanical strength, exhibits dihydrogen bonding with the difluoro(oxalate) borate anions, which is strong (high enthalpy penalty) and directional (low entropy penalty), thus restricting the migration of anions. As a result, the PCCE delivers a high ionic conductivity of 0.66 mS cm-1 with a high Li+ transference number (0.76) at 25 °C, as well as high oxidation stability. By an in situ polymerization approach, the PCCE enables LMBs using high-nikel LiNi0.8Co0.1Mn0.1O2 cathodes with a high capacity retention of 82.2% over 800 cycles with a cutoff voltage of 4.5 V and further LMBs using aggressive LiNi0.5Mn1.5O4 cathodes with a 96.4% capacity retention over 300 cycles with a cutoff voltage of 5.0 V. The described enthalpy-entropy manipulation approach offers a unique perspective for the molecular design of high-performance SPEs for high-energy Li metal batteries.

Development of multi-layered three-dimensional printed scaffold for sequential delivery of biomolecules

Spatiotemporal control of exogenous growth factors plays a crucial role in the sequential repair of damaged tissues. However, traditional therapeutic trials have mostly relied on the delivery of a single molecule because of the limitations of rapid diffusion and the instability of biomolecules. In this study, we developed a novel strategy using a composite of gelatin and silica as an alternative for the stable and sequential release of biomolecules. Two biomolecules, basic fibroblast growth factor and bone morphogenetic protein-2, were incorporated into two separate composites and sequentially layered onto the activated polymer surface. Each molecule was sequentially released from each layer of the scaffold and the silica composite prevented rapid diffusion owing to its nano-porous structure. The adhesion, proliferation, and osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells were significantly enhanced in the double-layered group containing separately delivered dual molecules compared with the control or single groups. Our developed gelatin&amp;ndash;silica composite was successfully placed in double layers on polymer scaffolds, and cellular responses were promoted in this manner. These results demonstrated that our scaffolding system has potential as a therapeutic strategy for the delivery of dual or multiple biomolecules in regenerative medicine. &amp;nbsp;

Ultra-High Purity and Productivity Separation of CO2 and C2H2 from CH4 in Rigid Layered Ultramicroporous Material.

Efficiently obtaining both high-purity gas-phase and adsorbed-phase products in a single physisorption process presents the challenge of simultaneously achieving high selectivity and uptake and rapid diffusion in adsorbents. With a focus on natural gas purification and high-purity acetylene production, we report for the first time that the synergistic ligand/anion binding mode and multiple diffusion pathways in a robust 2D layered ultramicroporous framework (ZUL-100) enable unprecedented carbon dioxide/methane and acetylene/methane separation performance. Taking advantage of its rich anion, functional ligand ,and rigid 3D interpenetrated ultramicroporous channels, ZUL-100 achieved record IAST selectivities for equimolar carbon dioxide/methane (3.2 × 105) and acetylene/methane (1.7 × 1010) mixtures, accompanied by record dynamic uptakes of carbon dioxide (3.10 mmol/g) and acetylene (4.79 mmol/g), respectively. The strong affinity and fast mass transfer of carbon dioxide and acetylene on ZUL-100 were systematically elucidated by a combination of in situ FTIR, single-crystal XRD, kinetic tests, and DFT-D adsorption/diffusion modeling. In particular, high-purity (≥99.999%) methane and carbon dioxide (acetylene) can both be obtained on ZUL-100 through a single adsorption-desorption cycle, with exceptional productivity (2.81-4.22 mmol/g of methane, 2.96 mmol/g of carbon dioxide, and 4.31 mmol/g of acetylene) and high yield (95.5% for carbon dioxide and 90.0% for acetylene).