RESUMO
Hydrogen energy is one of the most promising energy carriers to solve the increasingly severe energy crisis. Formic acid decomposition (FAD) solves the storage and transportation problems of hydrogen gas since hydrogen can be produced from aqueous formic acid under mild conditions. To efficiently convert formic acid to hydrogen gas, chemical and structural modification of Pd nanoparticles or supports have been carried out, especially introducing the strong metal support interaction (SMSI). Herein, we synthesized core-shell structured SiO2@SC compounds as the supports to introduce SMIS to Pd/PdO nanoparticles. The relationship between FAD activity and SMSI is investigated. The SMSI between Pd/PdO nanoparticles and SiO2/SC is adjusted by altering the thickness of the carbon layer. The X-ray photoelectron spectroscopy shows that owing to the strong electron-attracting ability SiO2 core contributes to leading the Pd0 active site in an electron-deficient state. The thickness of the carbon layer controls the ratio of Pd0/PdO, which enhances the anti-poisoning ability of the catalyst. Owing to the electron-deficient state of Pd0 and optimal ratio of Pd0/PdO, the hydrogen desorption rate of FAD on Pd is enhanced, and the turn over frequency of Pd/SiO2@SC-1:3 catalyst reaches 1138 h-1, which is ten times higher than that of the pristine Pd/SC catalyst. These results are believed to guide the design and development of highly active Pd-based catalysts for hydrogen generation via FAD.
RESUMO
Constructing heterojunction is an effective strategy to enhance photocatalytic performance of photocatalysts. Herein, we fabricated ZnTiO3/Bi4NbO8Cl heterojunction with improved performance via a typical mechanical mixing method. The rhodamine (RhB) degradation rate over heterojunction is higher than that of individual ZnTiO3 or Bi4NbO8Cl under Xenon-arc lamp irradiation. Combining ZnTiO3 with Bi4NbO8Cl can inhibit the recombination of photo-excited carriers. The improved quantum efficiency was demonstrated by transient-photocurrent responses (PC), electrochemical impedance spectroscopy (EIS), photoluminescence (PL) spectra, and time-resolved PL (TRPL) spectra. This research may be valuable for photocatalysts in the industrial application.