Efficient propane mineralization over unsaturated Pd cluster/CeO2 with prominent C-C cleavage capacity driven by inherent oxygen activation ability.

Light alkanes extensively presented in industrial exhausts have led tremendous harm to the atmospheric environment and human health. However, the catalytic destruction of light alkanes generally operates at elevated temperatures and the consequent reaction by-products are inevitably produced. It is therefore of great significance to engineer catalysts with superior thermal stability, internal activity and selectivity. Herein, we developed a Pd cluster/CeO 2 catalyst (Pd n /CeO 2) by a scalable deposition precipitation strategy, which demonstrates unexpected activity and thermal stability in the presence of 5% H 2 O attributing to abundant unsaturated Pd metal sites and excellent oxygen dissociation performance. Pd n /CeO 2 possesses a highly efficient C-C cleavage capability due to the persistent formation of a large number of oxygen vacancies. In comparison, the Pd 1 /CeO 2 catalyst, which is preferential for C-H bond cleavage and inactive for C-C bond cracking, produces remarkable hazardous organic by-products such as propyne and propylene, inhibiting the continuous decomposition of propane. The present study sheds critical insights into engineering efficient and stable catalysts for light alkane destruction. [Display omitted] • Strong metal-support interaction and unsaturated Pd sites were obtained on Pd n /CeO 2. • Pd cluster/CeO 2 (Pd n /CeO 2) exhibits high propane destruction ability and thermal stability. • Pd n /CeO 2 has excellent C-C cleavage ability owing to renewable oxygen vacancies. • The production of harmful organic by-products is effectively reduced over Pd n /CeO 2. • Saturated Pd single atom catalyst (Pd 1 /CeO 2) is preferentially for C-H bonds cleavage. [ABSTRACT FROM AUTHOR]