Publications by authors named "Shikang Yin"

Here, the clever design of forming an ohmic contact between SnS and MXene can regulate interfacial electron transport through Ti-O-Sn chemical bonds. This fast directional charge transport kinetics is attributed to the built-in electric field formed by the ohmic contact. As expected, the photoreduction CO activity of the optimized SSTC-5 catalyst is 10.

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The surge in anthropogenic CO emissions from fossil fuel dependence demands innovative solutions, such as artificial photosynthesis, to convert CO into value-added products. Unraveling the CO photoreduction mechanism at the molecular level is vital for developing high-performance photocatalysts. Here we show kinetic isotope effect evidence for the contested protonation pathway for CO photoreduction on TiO nanoparticles, which challenges the long-held assumption of electron-initiated activation.

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Photocatalytic mineralization of organic pollutions and simultaneously converting CO to CO (tetracycline → CO → CO) represents a fascinating way to solve the environmental and energy crisis. This work demonstrates the excellent mineralization and CO reduction performance of S-vacancy CdS and reveals the high efficiency of the carbon self-recycling two-in-one photocatalytic system.

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Figuring out the specific pathway of semiconductor-mediated proton-coupled electron transfer (PCET) driven by light is essential to solar energy conversion systems. In this work, we reveal that the amount of adsorbed water molecules determines the photo-induced PCET pathway on the TiO surface through systematic kinetic solvent isotope effect (KSIE) experiments. At low water content (<1.

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Achieving the intelligent controllability of the photocatalyst to the surrounding environment is a very meaningful work. Here, the polyacrylic acid (PAA) modified Ag/AgCl-40/CN composite was constructed to achieve an intelligent response of pH value. PAA exhibits hydrophilic properties at high pH value, increasing the adsorption capacity to tetracycline (TC) molecules.

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