Publications by authors named "Wuwan Xiong"

Photocatalytic reduction of CO to produce organic fuels is a promising strategy for addressing carbon reduction and energy scarcity. Transition metal carbides (TiCT ) are of particular interest due to their unique layered structures and excellent electrical conductivity. However, the practical application of TiCT is limited by the poor separation efficiency of photogenerated charge carriers and the low migration ability of photogenerated electrons.

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Recycling of spent lead-acid batteries (LABs) is extremely urgent in view of environmental protection and resources reuse. The current challenge is to reduce high consumption of chemical reagents. Herein, a closed-loop spent LABs paste (SLBP) recovery strategy is demonstrated through NaMoO consumption-regeneration-reuse.

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The application of small-pore chabazite-type SSZ-13 zeolites, key materials for the reduction of nitrogen oxides (NO) in automotive exhausts and the selective conversion of methane, is limited by the use of expensive ,,-trimethyl-1-ammonium adamantine hydroxide (TMAdaOH) as an organic structure-directing agent (OSDA) during hydrothermal synthesis. Here, we report an economical and sustainable route for SSZ-13 synthesis by recycling and reusing the OSDA-containing waste liquids. The TMAdaOH concentration in waste liquids, determined by a bromocresol green colorimetric method, was found to be a key factor for SSZ-13 crystallization.

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Rational construction of heterogeneous interfaces that maximize carrier flux and allow carrier separation for achieving efficient photocatalytic CO reduction still remain a challenge. In this work, high-throughput and intimate interfaces that allow efficient carrier separation and flux are designed by depositing high-density CeO nanoparticles on large-area TiCT (T = terminal group) nanosheets. Oxygen-containing functional groups of TiCT nanosheets facilitate the anchoring of CeO nanoparticles on the nanosheets via the formation of interfacial Ce-O-Ti bonds, which serve as effective channels for reverse and synergistic migration of electrons and holes to achieve spatial separation.

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BiMoO quantum dots (BM QDs, 5 nm in diameter) are evenly in situ grown on reduced graphene oxide (rGO) layers, sensitizing the graphene with high visible light response and activity for efficient solar light-driven CO reduction. Under irradiation, small-sized BM QDs generate active electrons and donate them to the rGO layers. Since the formation of BM QDs and the reduction of GO are undergone simultaneously, a close connection between BM QDs and rGO enables the electron injection from excited BiMoO QDs to graphene scaffolds, and abundant electrons accommodated by the rGO layers offer an electron-rich interface for CO reduction.

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