...
首页> 外文期刊>The Journal of Chemical Physics >Guided ion-beam studies of the kinetic-energy-dependent reactions of Co-n(+) (n=2-16) with D-2: Cobalt cluster-deuteride bond energies - art. no. 194320
【24h】

Guided ion-beam studies of the kinetic-energy-dependent reactions of Co-n(+) (n=2-16) with D-2: Cobalt cluster-deuteride bond energies - art. no. 194320

机译:Co-n(+)(n = 2-16)与D-2的动能依赖反应的导向离子束研究:钴簇-氘代键能-艺术。没有。 194320

获取原文
获取原文并翻译 | 示例
           

摘要

The kinetic-energy-dependent cross sections for the reactions of Co-n(+) (n=2-16) with D-2 are measured as a function of kinetic energy over a range of 0-8 eV in a guided ion-beam tandem mass spectrometer. The observed products are ConD+ for all clusters and ConD2+ for n = 4,5,9-16. 2 Reactions for the formation of ConD+ (n=2-16) and Co9D2+ are observed to exhibit thresholds, 2 whereas cross sections for the formation of ConD2+ (n=4,5,10-16) exhibit exothermic reaction 2 behavior. The Co-n(+)-D bond energies as a function of cluster size are derived from the threshold analysis of the kinetic-energy dependence of the endothermic reactions and are compared to previously determined metal-metal bond energies, D-0(Co-n(+)-Co). The bond energies of Co-n(+)-D generally increase as the cluster size increases, and roughly parallel those for Co-n(+)-Co for clusters n >= 4. These trends are explained in terms of electronic and geometric structures for the Co-n(+) clusters. The bond energies of Co-n(+)-D for larger clusters (n >= 10) are found to be very close to the value for chemisorption of atomic hydrogen on bulk-phase cobalt. The rate constants for D-2 chemisorption on the cationic clusters are compared with the results from previous work on cationic and neutral cobalt clusters. (c) 2005 American Institute of Physics.
机译:Co-n(+)(n = 2-16)与D-2反应的动能依赖截面是在离子引导下0-8 eV范围内随动能的函数而测得的。束串联质谱仪。对于所有群集,观察到的乘积为ConD +,对于n = 4,5,9-16,观察到的乘积为ConD2 +。 2观察到形成ConD +(n = 2-16)和Co9D2 +的反应显示阈值,而形成ConD2 +(n = 4,5,10-16)的横截面显示放热反应2行为。 Co-n(+)-D键能随簇大小的变化是从吸热反应的动能依赖性阈值分析得出的,并与先前确定的金属-金属键能D-0(Co -n(+)-Co)。 Co-n(+)-D的键能通常随簇尺寸的增加而增加,并且对于簇n> = 4的Co-n(+)-Co的键能大致平行。这些趋势用电子和几何学解释Co-n(+)簇的结构。发现较大簇(n> = 10)的Co-n(+)-D键能非常接近原子氢在本体相钴上的化学吸附值。将D-2在阳离子簇上的化学吸附速率常数与先前对阳离子和中性钴簇的研究结果进行比较。 (c)2005年美国物理研究所。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

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