Cu3(BTC)2 nanoflakes synthesized in an ionic liquid/water binary solvent and their catalytic properties.

Low-dimensional metal-organic frameworks (MOFs) exhibit enhanced properties compared with three-dimensional (3D) geometry MOFs in many fields. In this work, we demonstrate the synthesis of Cu3(BTC)2 (BTC = benzene-1,3,5-tricarboxylate) nanoflakes in a binary solvent of ionic liquid (IL) and water. Such a MOF architecture has a high surface area and abundant unsaturated coordination metal sites, making them attractive for adsorption and catalysis. For example, in catalyzing the oxidation reactions of a series of alcohols, the Cu3(BTC)2 nanoflakes exhibit a high performance that is superior to Cu3(BTC)2 microparticles synthesized in a conventional solvent. Experimental and theoretical studies reveal that the IL accelerates the crystallization of Cu3(BTC)2, while water plays a role in stripping the Cu3(BTC)2 blocks that are formed at an early stage through its attack on the crystal plane of Cu3(BTC)2. Such an in situ crystallization-exfoliation process that uses an IL/water solvent opens a new route for producing low-dimensional MOFs.

Anchoring Ionic Liquid in Copper Electrocatalyst for Improving CO2 Conversion to Ethylene.

Electrochemical conversion of CO2 to valuable fuels is appealing for CO2 fixation and energy storage. The Cu-based catalysts feature unique superiorities, but achieving high ethylene selectivity is still restricted. In this study, we propose the anchoring of an ionic liquid (IL) on a Cu electrocatalyst for improving the electrochemical CO2 reduction to ethylene. In a water-based electrolyte and a commonly used H-type cell, a high ethylene Faradaic efficiency of 77.3 % was achieved at -1.49 V (vs. RHE). Experimental and theoretical studies reveal that an IL can modify the electronic structure of a Cu catalyst through its interaction with Cu, making it more conducive to *CO dimerization for ethylene formation.

ZIF-9(III) nanosheets synthesized in ionic liquid/ethanol mixture for efficient photocatalytic hydrogen production.

To improve the photocatalytic performance of metal-organic frameworks is of great importance. We synthesized the nanosheets of a zeolitic imidazolate framework (ZIF-9(III)) in ionic liquid/ethanol solution, with an average thickness of 4.6 nm. The as-synthesized ZIF-9(III) nanosheets have optoelectronic properties superior to the three-dimensional ZIF-9(III) synthesized by the conventional solvothermal method. The ZIF-9(III) nanosheets exhibit high activity for photocatalytic hydrogen production under visible light irradiation. The maximum hydrogen production rate can reach 112.37 mmol g-1 h-1, while that by three-dimensional ZIF-9(III) is 29.64 mmol g-1 h-1 under the same experimental conditions.

Co(NO3)2/covalent organic framework nanoparticles for high-efficiency photocatalytic oxidation of thioanisole.

Herein, we demonstrated a highly efficient photocatalytic sulfide oxidation reaction at ambient conditions without a sacrificial reagent or redox mediator, by using Co(NO3)2/covalent organic framework nanoparticles as a photocatalyst.

SnS2/polypyrrole for high-efficiency photocatalytic oxidation of benzylamine.

Here, SnS2/polypyrrole (PPy) was synthesized, which shows high catalytic activity for the photocatalytic oxidation of benzylamine under mild conditions (at 25 °C, in air and without adding an additional sacrificial reagent, redox mediator and photosensitizer).

Periodically nanoporous hydrogen-bonded organic frameworks for high performance photocatalysis.

The development of highly catalytic hydrogen-bonded organic frameworks (HOFs) is of great importance, but remains challenging. Herein, we demonstrate the fabrication of a periodically nanoporous HOF for high performance photocatalysis. Compared with the conventional microporous HOFs, the nanoporous HOF architecture has a larger number of free carboxyl groups on the surface and presents greatly improved photoelectrochemical properties. It exhibits high catalytic activity for the photo-oxidative coupling of amines under mild conditions such as air atmosphere and room temperature and without any co-catalysts, sacrificial reagents or photosensitizers. The relationship between the structure, properties and catalytic performance of the nanoporous HOF was studied by experimental and theoretical investigations. It shows that such a HOF structure facilitates reactant adsorption and O2 dissociation, thus promoting the oxidative coupling reaction. This work provides a new way for improving the catalytic performance of a single HOF.

Supramolecular Calix[n]arenes-Intercalated Graphene Oxide Membranes for Efficient Proton Conduction.

Graphene oxide (GO) membranes with 2D interlaminar channels have triggered intensive interest as ion conductors. Incorporating abundant ion-conducting sites into GO interlayers is recognized as an effective strategy to facilitate ion conduction. Herein, we designed supramolecular compounds, para-sulphonato-calix[n]arenes (p-SC[n]As), as versatile intercalators to acquire highly conductive and robust GO membranes. The SC[n]A with ultrahigh ionic exchange capacity (IECw, 5.37 mmol g-1) imparts sufficient proton donors, and its rigid framework imparts strong support of adjacent nanosheets. We designed three kinds of SC[n]As with the same IECw but different sizes as intercalators, endowing the GO/SC[n]A membranes with increasing ion concentration and d-spacing in the order of GO/SC[4]A < GO/SC[6]A < GO/SC[8]A. Therefore, the interlayers of GO/SC[8]A membranes afforded higher density of proton donors and could accommodate more water molecules to construct more continuous H-bond networks for proton transfer. Accordingly, the proton conductivities exhibited the same increasing trend, up to 327.0 mS cm-1 of GO/SC[8]A-30% at 80 °C, 100% RH, which was 2.80 times higher than that of the GO membrane. Moreover, the GO/SC[n]A membranes remained stable in wet state, along with a 66% elevation in mechanical performance compared to the GO membrane.

Control of Edge/in-Plane Interactions toward Robust, Highly Proton Conductive Graphene Oxide Membranes.

Graphene oxide (GO) membrane, bearing well-aligned interlayer nanochannels and well-defined physicochemical properties, promises fast proton transport. However, the deficiency of proton donor groups on the basal plane of GO and weak interlamellar interactions between the adjacent nanosheets often cause low proton conduction capability and poor water stability. Herein, we incorporate sulfonated graphene quantum dots (SGQD) into  GO membrane to solve the above dilemma via synergistically controlling the edge electrostatic interaction and in-plane π-π interaction of SGQD with GO nanosheets. SGQD with three different kinds of electron-withdrawing groups are employed to modulate the edge electrostatic interactions and improve the water swelling resistant property of GO membranes. Meanwhile, SGQD with abundant proton donor groups assemble on the sp2 domain of GO via in-plane π-π interaction and confer the GO membranes with low-energy-barrier proton transport channels. As a result, the GO membrane achieves an enhanced proton conductivity of 324 mS cm-1, maximum power density of 161.6 mW cm-2, and superior water stability when immersed into water for one month. This study demonstrates a strategy for independent manipulation of conductive function and nonconductive function to fabricate high-performance proton exchange membranes.

Highly Hydroxide-Conductive Nanostructured Solid Electrolyte via Predesigned Ionic Nanoaggregates.

The creation of interconnected ionic nanoaggregates within solid electrolytes is a crucial yet challenging task for fabricating high-performance alkaline fuel cells. Herein, we present a facile and generic approach to embedding ionic nanoaggregates via predesigned hybrid core-shell nanoarchitecture within nonionic polymer membranes as follows: (i) synthesizing core-shell nanoparticles composed of SiO2/densely quaternary ammonium-functionalized polystyrene. Because of the spatial confinement effect of the SiO2 "core", the abundant hydroxide-conducting groups are locally aggregated in the functionalized polystyrene "shell", forming ionic nanoaggregates bearing intrinsic continuous ion channels; (ii) embedding these ionic nanoaggregates (20-70 wt %) into the polysulfone matrix to construct interconnected hydroxide-conducting channels. The chemical composition, physical morphology, amount, and distribution of the ionic nanoaggregates are facilely regulated, leading to highly connected ion channels with high effective ion mobility comparable to that of the state-of-the-art Nafion. The resulting membranes display strikingly high hydroxide conductivity (188.1 mS cm-1 at 80 °C), which is one of the highest results to date. The membranes also exhibit good mechanical properties. The independent manipulation of the conduction function and nonconduction function by the ionic nanoaggregates and nonionic polymer matrix, respectively, opens a new avenue, free of microphase separation, for designing high-performance solid electrolytes for diverse application realms.

Bioinspired Ultrastrong Solid Electrolytes with Fast Proton Conduction along 2D Channels.

Solid electrolytes have attracted much attention due to their great prospects in a number of energy- and environment-related applications including fuel cells. Fast ion transport and superior mechanical properties of solid electrolytes are both of critical significance for these devices to operate with high efficiency and long-term stability. To address a common tradeoff relationship between ionic conductivity and mechanical properties, electrolyte membranes with proton-conducting 2D channels and nacre-inspired architecture are reported. An unprecedented combination of high proton conductivity (326 mS cm-1 at 80 °C) and superior mechanical properties (tensile strength of 250 MPa) are achieved due to the integration of exceptionally continuous 2D channels and nacre-inspired brick-and-mortar architecture into one materials system. Moreover, the membrane exhibits higher power density than Nafion 212 membrane, but with a comparative weight of only ≈0.1, indicating potential savings in system weight and cost. Considering the extraordinary properties and independent tunability of ion conduction and mechanical properties, this bioinspired approach may pave the way for the design of next-generation high-performance solid electrolytes with nacre-like architecture.