Structural evolution of a metal–organic framework and derived hybrids composed of metallic cobalt and copper encapsulated in nitrogen-doped porous carbon cubes with high catalytic performance. Issue 1 (30th November 2016)

• Record Type: Journal Article
• Authors: Li, Hui; Yue, Fan; Yang, Chao; Xue, Peng; Li, Nannan; Zhang, Yi; Wang, Jide
• Is Part Of: CrystEngComm. Volume 19:Issue 1(2017)
• Page Start: 64
• Page End: 71
• Publication Date: 2016-11-30
• Subjects: Crystals -- Periodicals; Crystal growth -- Periodicals; Crystallography -- Periodicals; Cristaux -- Périodiques; Cristaux -- Croissance -- Périodiques; Cristallographie -- Périodiques; 548
• DOI: 10.1039/c6ce01995a
• Languages: English
• ISSNs: 1466-8033

Abstract

Abstract : Metal residues confined inside the graphitic carbon layers change the work function of shells and exhibit surprisingly high chemical activities. Abstract : We present here the structural evolution of a Prussian blue analogue Cu II 3 [Co III (CN)6 ]2 (Cu–Co PBA) controlled by sodium citrate as a function of time at room temperature. We identified the different stages of Cu–Co PBA formation and elucidated its transformation kinetics. Moreover, 3D hybrid composites of nitrogen-doped porous carbon cubes, with cobalt and copper nanoparticles embedded within the well-graphitized shells, were rationally fabricated using Cu–Co PBA as the single precursor. The resulting Cu/Co@NPCC catalysts showed superior catalytic activity in the reduction of 4-nitrophenol to 4-aminophenol. Metallic cobalt and copper cores were leached out by FeCl3 and HCl treatment to determine the catalytically active sites. Results showed that the nitrogen-doped porous carbon still exhibited excellent catalytic performance after the metallic cores were removed. Based on the experimental results, we speculate that the unique structure of metal residues encapsulated inside the graphitic carbon layers may have higher catalytic activity than the metal particles themselves.