Related Experiment Video
Updated: Feb 26, 2026

Tuning the Acidity of Pt/ CNTs Catalysts for Hydrodeoxygenation of Diphenyl Ether
Published on: August 17, 2019
Unique Facet Effects of Metastable Pt/TiO2 Catalysts in Water Activation for VOCs Degradation
Shaodi Sun1, Zhuang Wang1, Siyu Liu1
1Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen 361005, PR China.
Abstract:
The treatment of industrial-sourced VOCs (Volatile Organic Compounds) stands as a pivotal research topic within the realm of environmental catalysis. The intricate composition of VOCs, especially the presence of H2O, frequently undermines the catalysts in the treatment systems. In this study, we have explored metastable catalysts that are regulated by different facets, which can activate H2O into active oxygen species required for the reaction. Surprisingly, the sample with the {101} facet exposed demonstrates superior performance compared to the sample with the high-energy {001} facet with H2O. In fact, the metastable structures constructed from diverse atomic arrangements are the key to breaking through this conventional understanding. Although the emergence of 18OCO18 indicates that all samples can achieve the H2O process, the Pt/TiO2-MS {101} sample, with its longer M-O bonds and more Pt-Ometa-Ti, exhibits lower H2O dissociation energy and stronger lattice oxygen mobility. In contrast, the high-energy facets and the increased Pt0 endow the Pt/TiO2-MS {001} sample with a stronger ability to activate O2. The distinct catalytic behaviors displayed by the metastable structures with different facets exposed offer fresh strategies for designing highly efficient catalysts.
More Related Videos
Related Concept Videos
Catalysis
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.

