ZnO-Fe₂O₃ mixed oxides and supported gold nanocatalysts were prepared by using coprecipitation and deposition–precipitation methods, respectively. Cinnamaldehyde hydrogenation over various ZnO-Fe₂O₃ mixed oxides supported gold nanocatalysts have been investigated at 140 °C and a hydrogen pressure of 1.0 MPa. The molar ratio of Fe to Zn was found to greatly affect the selective hydrogenation catalytic activity of ZnO-Fe₂O₃ mixed oxide supported gold nanocatalysts. Among these supported gold nanocatalysts in this work, Au/Zn_0.7Fe_0.3O_x (Au loading of 1.74 wt %) exhibited the highest conversion of cinnamaldehyde and high selectivity to cinnamal alcohol. The excellent catalytic activity of Au/Zn_0.7Fe_0.3O_x was tightly associated with a large surface area, small gold nanoparticles, and good H₂ dissociation ability at low temperature.

Significant research has focused on cost–effective, highly active, and exceptionally stable non–noble metal electrocatalysts (NNMEs) to boost the performance of the oxygen reduction reaction (ORR). Of note, the development of design and synthesis of Fe–N–C electrocatalysts is essential but remains challenging. Herein, the Fe and N co–doped porous carbon material with a yolk–shell (YS) structure, termed SA–H₂TPyP@PDA–Fe (900), was fabricated by self–assembly of metal–free porphyrin as a yolk and polymerization of dopamine as a shell with an addition of iron salts, followed by the high–temperature pyrolysis and acid–leaching. As a result, active sites, like FeN₄ and N–doped C, within rich porous YS carbon structures, play an important role for ORR in an alkaline media. The SA–H₂TPyP@PDA–Fe (900) electrocatalyst shows positive ORR performances than those of SA–H₂TPyP (900) and SA–H₂TPyP@PDA (900), indicating the dominating function of the YS carbon structure decorated with Fe–based species. This efficient route of template–free–induced preparation of the YS structure discovers the design and synthesis of NNMEs for ORR.