Study on High Activity and Outstanding Stability of Hollow-NiPt@SiO(2) Core–Shell Structure Catalyst for DRM Reaction

A neoteric hollow-NiPt@SiO(2) core–shell structure catalyst with 7-nm-sized hollow NiPt alloy nanoparticle (NP) packaged by SiO(2) shell was prepared by a classic Stober method. Compared with hollow-NiPt/SiO(2) supported catalyst, the hollow-NiPt@SiO(2) core–shell catalyst exhibited better activity and thermal stability in dry reforming of methane (CH(4)) (DRM) with CO(2) reaction, with CH(4)/CO(2) conversion to 97% and service life to 200 h at 800°C, respectively. In addition, the activity and stability of core–shell catalysts with different nuclei were tested. In contrast to the continuous deactivation of the supported catalyst, all the core–shell catalysts were able to maintain stability for 200 h, and the activity sequence was Hollow-NiPt > NiPt NPs > Pt NPs > Ni NPs. By characterization, we learned that hollow structure had an inner surface and thus had a larger active specific surface area than NP structure. In addition, NiPt NPs had better activity than Ni NPs and Pt NPs because Ni and Pt formed as alloy in NiPt NPs. Therefore, the efficient and thermally stable hollow-NiPt@SiO(2) core–shell catalyst has a promising application prospect in DRM reaction and can make a considerable contribution to the sustainable use of energy.