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Designing S-scheme heterojunctions is an effective method to improve the charge localization on the surface of photocatalysts. Their effective charge transport routes can be enhanced with the help of interfacial noble metal nanoparticles. Herein, an Ag/CuO@ZnIn 2 S 4 plasma S-scheme heterojunction with heterogeneous interfacial covalent bonds was successfully designed. The 15% Ag/CuO@ZnIn 2 S 4 has promising photocatalytic performance and stability with the highest CO and CH 4 yields of 6.9 and 54.4 µmol g−1 h−1 and CH 4 selectivity of 92.8%. It is evidenced that the photogenerated charge can be efficiently separated and transported due to the influence of both the S-scheme electron migration mode and the Cu-S covalent bond. The process is further accelerated by using precious metals as cocatalysts, which can then selectively convert CO 2 into CH 4. This research is expected to provide helpful information for engineering S-scheme heterojunction photocatalysts and investigating their charge transfer kinetics. [Display omitted] • Design of a S-scheme heterojunction to promote the separation of carriers. • Built the Cu-S bonds to accelerate the transfer of charges. • Utilizing the LSPR effect to generate hot electrons and enhance light absorption. • The Ag/CuO@ZnIn 2 S 4 photocatalysts can selectively reduce CO 2 to CH 4. [ABSTRACT FROM AUTHOR]

Electrochemical hydrogen production coupling upgrading of organic substances has been regarded as a promising approach to harvest both green energy and commodity products. However, the competition of oxygen evolution reaction always limits the transformation of organics and the research on this mutually restricted relationship was less focused. Herein, an amorphous layered double hydroxide (LDH) rich in active oxygen is well-constructed, which realizes the glycerol oxidation with nearly 100 % faradaic efficiency and high formic acid production yield at a current density > 200 mA cm−2. In-situ monitoring combined with electrochemical probe confirms that the active oxygen on the amorphous LDHs promotes the deprotonation of glycerol. To further reduce the energy input, an alkaline-acid hybrid flow cell is built to achieve constant hydrogen production coupling formic acid production at high current density (100 mA cm−1) under an ultra-low cell voltage of 0.90 V with high durability for over 500 h. Moreover, a novel waste oil recycle path is developed to transform waste oil into target value-added products (potassium diformate (KDF) and biodiesel) and hydrogen fuels using the amorphous LDHs electrocatalysts. [Display omitted] • An amorphous layered double hydroxide (A-NiFe-LDH) rich in active oxygen was prepared via electrochemical amorphization. • A-NiFe-LDH can boost electrochemical glycerol oxidation coupling hydrogen production. • The existence of multiple active oxygen species (AOS) and AOS involved oxidation mechanism is uncovered. • A new cycling path of waste oil into target value-added products is designed. [ABSTRACT FROM AUTHOR]