No abstract

Layered rare-earth hydroxides (LREHs), as a series of special lamellar compounds having a similar structure to layered double hydroxides (LDHs), are becoming a new type of catalyst materials. In this study, we have prepared a series of uniform LREH (RE = Y, La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, and Tm) nanosheets through a reverse-microemulsion method. After deposition–precipitation of HAuCl4 and calcination, supported Au catalysts (denoted as Au/LREO) were subsequently obtained. The catalytic properties of all the derived Au/LREO catalysts were evaluated by aerobic conversion of glycerol to lactic acid under mild conditions (90 °C, 1 atm). Among these catalysts, Au/LPrO displays the best performances, including the highest glycerol conversion, lactic acid, and C3 product selectivity. Both the catalytic activities and the characterizations of the structure of Au/LREO indicate that the kind of rare-earth ions plays a key role in determining the Au particle size and its valence state and reducibility, which are the important factors correlated with the catalytic activities in glycerol conversion. In fact, the three features of gold particles, the extra-small size (∼3 nm), high content of Au0 species, and high reducibility, are the essential prerequisites for achieving the superior catalytic performance of Au/LPrO.

Catalytic selective oxidation of glucose into value-added gluconic acid is one of the sustainable routes for biomass utilization, for which the supported Au catalysts have been widely explored. Au/CeO2 was...

No abstract

The selective oxidation of glycerol holds promise to transform glycerol into value-added chemicals. However, it remains a big challenge to achieve satisfactory selectivity toward the specific product at high conversion due to the multiple reaction pathways. Here, we prepare a hybrid catalyst via supporting Au nanoparticles on CeMnO3 perovskite with a modest surface area, achieving promoted conversion of glycerol (90.1%) and selectivity of glyceric acid (78.5%), which are much higher than those of CeMnO x solid-solution-supported Au catalysts with larger surface area and other Ce-based or Mn-based Au catalysts. The strong interaction between Au and CeMnO3 perovskite facilitates the electron transfer from the B-site metal (Mn) in the CeMnO3 perovskite to Au and stabilizes Au nanoparticles, which results in the enhanced catalytic activity and stability for glycerol oxidation. Valence band photoemission spectral analysis reveals that the uplifted d-band center of Au/CeMnO3 promotes the adsorption of the glyceraldehyde intermediate on the catalyst surface, which benefits further oxidation of glyceraldehyde into glyceric acid. The flexibility of the perovskite support provides a promising strategy for the rational design of high-performance glycerol oxidation catalysts.