首页> 美国卫生研究院文献>Frontiers in Chemistry >Highly Active Ni- and Co-Based Bimetallic Catalysts for Hydrogen Production From Ammonia-Borane
【2h】

Highly Active Ni- and Co-Based Bimetallic Catalysts for Hydrogen Production From Ammonia-Borane

机译:高活性镍和钴基双金属催化剂,用于从氨硼烷生产氢气

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Ammonia-borane is one of the most promising candidates for hydrogen carriers. A series of Ni- and Co-based bimetallic catalysts supported on SiO2 (Ni–M/SiO2 and Co–M/SiO2; M = Ga, Ge, Sn, Zn) was prepared and tested as catalysts for hydrogen production from ammonia-borane (AB) in water or methanol. Ni–Zn/SiO2 and Co–Ge/SiO2 exhibited catalytic activities much higher than those of monometallic Ni/SiO2 and Co/SiO2, respectively. Ni–Zn/SiO2 showed a high catalytic activity when water was used as a solvent, where the reaction was completed within 6 min at room temperature with a specific reaction rate of 4.3 ml min−1 mmol-cat−1 mM-AB−1. To the best of our knowledge, this is the highest value among those reported using 3d metal-based catalysts. Co–Ge/SiO2 afforded a five-fold higher reaction rate than that of the corresponding monometallic Co/SiO2. XRD, TEM, and HAADF-STEM-EDS analyses revealed that Ni0.75Zn0.25 and Co0.8Ge0.2 solid-solution alloys were formed with high phase purities. An XPS study showed that Co atoms in Co0.8Ge0.2 were electron-enriched due to electron transfer from Ge to Co, which may be the origin of the improved catalytic activity.
机译:氨硼烷是氢载体最有希望的候选者之一。制备了一系列负载在SiO2上的Ni和Co基双金属催化剂(Ni–M / SiO2和Co–M / SiO2; M = Ga,Ge,Sn,Zn),并用作由氨硼烷生产氢气的催化剂(AB)在水中或甲醇中。 Ni-Zn / SiO2和Co-Ge / SiO2分别显示出比单金属Ni / SiO2和Co / SiO2更高的催化活性。 Ni-Zn / SiO2在以水为溶剂时表现出较高的催化活性,该反应在室温下于6分钟内完成,比反应速率为4.3 ml min -1 mmol-cat -1 mM-AB -1 。据我们所知,这是使用3d金属基催化剂报道的最高值。 Co-Ge / SiO2的反应速率比相应的单金属Co / SiO2的反应速率高五倍。 XRD,TEM和HAADF-STEM-EDS分析表明,形成的Ni0.75Zn0.25和Co0.8Ge0.2固溶合金具有高相纯度。 XPS研究表明,由于电子从Ge转移到Co,Co0.8Ge0.2中的Co原子被电子富集,这可能是提高催化活性的根源。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号