密度泛函理论
自然键轨道
材料科学
吸附
轨道杂交
化学物理
反键分子轨道
碳纳米管
催化作用
计算化学
结合能
兴奋剂
态密度
分子
原子轨道
分子轨道
物理化学
纳米技术
化学
原子物理学
分子轨道理论
有机化学
电子
凝聚态物理
量子力学
光电子学
物理
出处
期刊:International Journal of Modern Physics C
[World Scientific]
日期:2015-12-01
卷期号:27 (07): 1650075-1650075
被引量:3
标识
DOI:10.1142/s0129183116500753
摘要
The adsorption behavior and electronic properties of CO and O 2 molecules at the supported Pt and Eu atoms on (5,5) armchair SWCNT have been systematically investigated within density functional theory (DFT). Fundamental aspects such as adsorption energy, natural bond orbital (NBO), charge transfer, frontier orbitals and the projected density of states (PDOS) are elucidated to analyze the adsorption properties of CO and O 2 molecules. The results reveal that B- and N-doping CNTs can enhance the binding strength and catalytic activity of Pt (Eu) anchored on the doped-CNT, where boron-doping is more effective. The electronic structures of supported metal are strongly influenced by the presence of gases. After adsorption of CO and O 2 , the changes in binding energy, charge transfer and conductance may lead to the different response in the metal-doped CNT-based sensors. It is expected that these results could provide helpful information for the design and fabrication of the CO and O 2 sensing devices. The high catalytic activity of Pt supported at doped-CNT toward the interaction with CO and O 2 may be attributed to the electronic resonance particularly among Pt-5d, CO-2[Formula: see text]* and O 2 -2[Formula: see text]* antibonding orbitals. In contrast to the supported Eu at doped-CNT, the Eu atom becomes more positively charged, which leads to weaken the CO adsorption and promote the O 2 adsorption, consequently enhancing the activity for CO oxidation and alleviating the CO poisoning of the europium catalysts. A notable orbital hybridization and electrostatic interaction between these two species in adsorption process being an evidence of strong interaction. The electronic structure of O 2 adsorbed on Eu-doped CNT resembles that of O[Formula: see text], therefore the transferred charge weakens the O–O bonds and facilitates the dissociation process, which is the precondition for the oxygen reduction reaction (ORR).
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