A confined thermal transformation strategy to synthesize single atom catalysts supported on nitrogen-doped mesoporous carbon nanospheres for selective hydrogenation. Issue 45 (9th November 2021)

• Record Type: Journal Article
• Authors: Tian, Zhengbin; Wang, Wenquan; Zheng, Yan; Wang, Guang-Hui
• Is Part Of: Journal of materials chemistry. Volume 9:Issue 45(2021)
• Page Start: 25488
• Page End: 25494
• Publication Date: 2021-11-09
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d1ta08365a
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Pd single atoms supported on nitrogen-doped mesoporous carbon nanospheres (Pd1 /NMCS) are prepared by a confined thermal transformation strategy, and show excellent performance for selective hydrogenation of quinoline to 1, 2, 3, 4-tetrahydroquinoline. Abstract : Carbon-supported single-atom catalysts (SACs) have brought considerable attention to heterogeneous catalysis, but they, however, often suffer from low activity due to the mass transfer limitation. Herein, we report a soft-templating method to synthesize core–shell mesostructured polymer nanospheres with metal nanoclusters (M-NCs, M = Pd, Pt) as the core, which can be easily converted into nitrogen-doped mesoporous carbon nanosphere (NMCS) supported SACs (M1 /NMCS) after a confined thermal transformation process. Through this strategy, Pd1 /NMCS and Pt1 /NMCS are successfully prepared with rich porosity and high N content. The abundant N species in M1 /NMCS can be employed as anchoring sites to capture and stabilize the single metal atoms. In addition, the mesoporous structure of M1 /NMCS is beneficial for the mass transfer and the exposure of active sites. Benefiting from such a unique structure, the as-obtained Pd1 /NMCS exhibits excellent activity, selectivity, and long-term stability in the selective hydrogenation of quinoline.