Qiu Fangyuan, Li Li, Liu Guang, Xu Changchang, An Cuihua, Xu Yanan, Wang Ying, Huang Yanan, Chen Chengcheng, Wang Yijing, Jiao Lifang, Yuan Huatang
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Key Laboratory of Advanced Energy Materials Chemistry (MOE), Institute of New Energy Material Chemistry, Tianjin Key Lab on Metal and Molecule-Based Material Chemistry, Nankai University, Tianjin, 30007 (P.R. China), Fax: (+86) 22-23503639.
Chem Asian J. 2014 Feb;9(2):487-93. doi: 10.1002/asia.201301034. Epub 2013 Nov 22.
Size-controlled Ag0.04@Co0.48@Ni0.48 core-shell nanoparticles (NPs) were synthesized by employing graphene (rGO) with different reduction degrees as supports. The number of C=O and C=O functional groups on the surface of rGO might play a major role in controlling the particle size. The strong steric-hindrance effect of C=O resulted in the growth of large particles, whereas C=O contributed to the formation of small particles. The particle size of Ag0.04@Co0.48@Ni0.48 NPs supported on rGO with different reduction degrees decreased as the number of C=O functional groups decreased. The decrease in the particle size probably led to the increase in the catalytic activity towards the hydrolysis of ammonia borane (AB). The enhanced catalytic activity largely stemmed from the increasing active sites on the surface of catalysts owing to the decreasing particle size.
通过使用具有不同还原度的石墨烯(rGO)作为载体,合成了尺寸可控的Ag0.04@Co0.48@Ni0.48核壳纳米颗粒(NPs)。rGO表面C=O和C=O官能团的数量可能在控制颗粒尺寸方面起主要作用。C=O的强空间位阻效应导致大颗粒生长,而C=O有助于小颗粒的形成。随着C=O官能团数量的减少,负载在不同还原度rGO上的Ag0.04@Co0.48@Ni0.48 NPs的粒径减小。粒径的减小可能导致对氨硼烷(AB)水解的催化活性增加。催化活性的增强主要源于粒径减小导致催化剂表面活性位点增加。