摘要
以Na BH4为还原剂合成了具有核壳结构的Cu@Co纳米颗粒,研究了其催化氨硼烷水解放氢性能。结果表明,Cu和Co的比例不同,Cu@Co纳米颗粒的催化活性也不同,其中Cu0.2@Co0.8的催化活性最高,室温下最大放氢速率达1364 m L min-1 g-1,活化能为59.1k J mol-1。Cu0.2@Co0.8催化氨硼烷水解反应对催化剂浓度是一级反应,对氨硼烷浓度为零级反应。Cu@Co核壳结构在催化反应中比Cu Co合金能够提供更多的反应活性位点,而且单质铜和钴之间存在的协同作用和电子效应在提高催化性能方面起着关键作用。
Non - noble metal Cu@ Co core - shell nanoparticles (NPs) containing a Cu core and a Co shell were synthesized by a facile chemical reduction method. In a,ddition, the catalytic performance for hydrolysis of ammonia borane (AB) was investigated. The results show that the catalytic activity of Cu@ Co NPs depend on the ratios of copper and cobalt. Among them, Cu0.2@ Co0.8 showed the best catalytic activity, with a high hydrogen generation rate of 1364 mL min^-1g^-1 at 298 K and the lower active energy of 59.1 kJ mol^-1. The dehydrogenation kinetic studies indicate that the hydrolysis of AB catalyzed by Cu0.2 @ Coo. s is first order with respect to the catalyst concentration, and it is zero - order with respect to the concentration of AB. Cu@ Co core shell nanoparticles provide more active sites on the surface to facilitate the catalytic reaction than CuCo alloy. Furthermore, the synergetic interaction and electronic effect between Cu and Co in Cu0.2@ Co0.8 play a critical role in the enhanced catalytic activity.
出处
《功能材料与器件学报》
CAS
2015年第4期7-12,共6页
Journal of Functional Materials and Devices
基金
863计划(2012AA051503
2012AA051901)
国家自然科学基金(51271094
51371100)
天津科技计划(12JCQNJC03900
13JCZDJC26500)
先进能源材料化学"111计划"(B12015)资助
关键词
核壳结构
Cu@Co纳米颗粒
氨硼烷
水解
core - shell structure
Cu@ Co nanoparticles
ammonia borane
hydrolysis