Publications by authors named "Wen-Gang Cui"

Hydrogen electrocatalytic reactions, including the hydrogen evolution reaction (HER) and the hydrogen oxidation reaction (HOR), play a crucial role in a wide range of energy conversion and storage technologies. However, the HER and HOR display anomalous non-Nernstian pH dependent kinetics, showing two to three orders of magnitude sluggish kinetics in alkaline media compared to that in acidic media. Fundamental understanding of the origins of the intrinsic pH effect has attracted substantial interest from the electrocatalysis community.

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Non-dissociative chemisorption solid-state storage of hydrogen molecules in host materials is promising to achieve both high hydrogen capacity and uptake rate, but there is the lack of non-dissociative hydrogen storage theories that can guide the rational design of the materials. Herein, we establish generalized design principle to design such materials via the first-principles calculations, theoretical analysis and focused experimental verifications of a series of heteroatom-doped-graphene-supported Ca single-atom carbon nanomaterials as efficient non-dissociative solid-state hydrogen storage materials. An intrinsic descriptor has been proposed to correlate the inherent properties of dopants with the hydrogen storage capability of the carbon-based host materials.

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The identification of heavy metal sources in farmland soils is essential for the rational health condition management and sustainable development of soil. Using source resolution results(source component spectrum and source contribution)of a positive matrix factorization(PMF)model, historical survey data, and time-series remote sensing data, integrating a geodetector(GD), an optimal parameters-based geographical detector(OPGD), a spatial association detector(SPADE), and an interactive detector for spatial associations(IDSA)model, this study explored the modifiable areal unit problem(MAUP) of spatial heterogeneity of soil heavy metal sources and identified the driving factors and their interacting effects on the spatial heterogeneity of soil heavy metal sources in categorical and continuous variables, respectively. The results showed that the spatial heterogeneity of soil heavy metal sources at small and medium scales was affected by the spatial scale, and the optional spatial unit was 0.

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As a straightforward way to fix solar energy, photo/photothermal catalysis with semiconductor provides a promising way to settle the energy shortage and environmental crisis in many fields, especially in clean energy conversion. Topologically porous heterostructures (TPHs), featured with well-defined pores and mainly composed by the derivatives of some precursors with specific morphology, are a major part of hierarchical materials in photo/photothermal catalysis and provide a versatile platform to construct efficient photocatalysts for their enhanced light absorption, accelerated charges transfer, improved stability, and promoted mass transportation. Therefore, a comprehensive and timely review on the advantages and recent applications of the TPHs is of great importance to forecast the potential applications and research trend in the future.

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Al ion batteries (AIBs) are attracting considerable attention owing to high volumetric capacity, low cost, and high safety. However, the strong electrostatic interaction between Al and host lattice leads to discontented cycling life and inferior rate capability. Herein, a new strategy of employing water molecules contained VOPO ·H O to boost Al migration via the charge shielding effect of water is reported.

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Direct hydrogenation of CO  to methanol using green hydrogen has emerged as a promising method for carbon neutrality, but qualifying catalysts represent a grand challenge. In O /ZrO  catalyst has been extensively applied in methanol synthesis due to its superior activity; however, the electronic effect by strong oxides-support interactions between In O  and ZrO  at the In O /ZrO  interface is poorly understood. In this work, abundant In O /ZrO  heterointerfaces are engineered in a hollow-structured In O @ZrO  heterostructure through a facile pyrolysis of a hybrid metal-organic framework precursor MIL-68@UiO-66.

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Selective hydrogenation of CO to methanol is a "two birds, one stone" technology to mitigate the greenhouse effect and solve the energy demand-supply deficit. Cu-based catalysts can effectively catalyze this reaction but suffer from low catalytic stability caused by the sintering of Cu species. Here, we report a series of zeolite-fixed catalysts Cu/ZnO()@Na-ZSM-5 ( is the mass ratios of Cu/Zn in the catalysts) with core-shell structures to overcome this issue and strengthen the transformation.

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The design and development of efficient catalytic materials with synergistic catalytic sites always has long been known to be a thrilling and very dynamic research field. Crystalline porous materials (CPMs) mainly including metal-organic frameworks and zeolites with high scientific and industrial impact have recently been the subject of extensive research due to their essential role in modern chemical industrial processes. The rational incorporation of guest species in CPMs can synergize the respective strengths of these components and allow them to collaborate with each other for synergistic catalysis, leading to enhanced catalytic activity, selectivity, and stability in a broad range of catalytic processes.

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Solid-liquid separation of similarly sized organic molecules utilizing sorbents offers the potential for new energy-efficient approaches to a number of important industrial separations such as xylenes (C8) separations. Research on selective C8 sorption has tended to focus upon rigid porous materials such as zeolites and MOFs but has revealed generally weak selectivity that is inconsistent across the range of C8 molecules. Nevertheless, there are a few recent examples of non-porous molecular materials that exhibit relatively high selectivity for -xylene (X) from X/X, approaching that of the current benchmark X sorbent, the zeolite H/ZSM-5.

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The separation and purification of light hydrocarbons (LHs) mixtures is one of the most significantly important but energy demanding processes in the petrochemical industry. As an alternative technology to energy intensive traditional separation methods, such as distillation, absorption, extraction, etc., adsorptive separation using selective solid adsorbents could potentially not only lower energy cost but also offer higher efficiency.

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