| H2分子在LaFeO3表面吸附的第一性原理研究 |
| First Principles Study on the Adsorption of H2 Molecules on LaFeO3 Surface |
| 作者 | 单位 | E-mail | | 陈玉红 | 兰州理工大学省部共建有色金属先进加工与再利用国家重点实验室, 兰州 730050
兰州理工大学理学院, 兰州 730050 | chenyh@lut.cn | | 潘昌昌 | 兰州理工大学省部共建有色金属先进加工与再利用国家重点实验室, 兰州 730050
兰州理工大学理学院, 兰州 730050 | | | 张梅玲 | 兰州理工大学理学院, 兰州 730050 | | | 元丽华 | 兰州理工大学理学院, 兰州 730050 | | | 张材荣 | 兰州理工大学省部共建有色金属先进加工与再利用国家重点实验室, 兰州 730050
兰州理工大学理学院, 兰州 730050 | | | 康龙 | 兰州理工大学省部共建有色金属先进加工与再利用国家重点实验室, 兰州 730050 | | | 罗永春 | 兰州理工大学省部共建有色金属先进加工与再利用国家重点实验室, 兰州 730050 | |
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| 摘要: 基于密度泛函理论的第一性原理方法,通过计算表面能确定LaFeO3(010)表面为最稳定的吸附表面,研究了H2分子在LaFeO3(010)表面的吸附性质。LaFeO3(010)表面存在LaO和FeO2两种终止表面,但吸附主要发生在FeO2终止表面,由于LaFeO3(010)表面弛豫的影响,使得凹凸不平的表面层增加了表面原子与H原子的接触面积,表面晶胞的纵向体积增加约2.5%,有利于H原子向晶体内扩散。研究发现,H2分子在LaFeO3(010)表面主要存在3种化学吸附方式:第一种吸附发生在O-O桥位,2个H原子分别吸附在2个O原子上,形成2个-OH基,这是最佳吸附位置,此时H原子与表面O原子的作用主要是H1s与O2p轨道杂化作用的结果,H-O之间为典型的共价键。H2分子的解离能垒为1.542eV,说明表面需要一定的热条件,H2分子才会发生解离吸附;第二种吸附发生在Fe-O桥位,1个H原子吸附在O原子上形成1个-OH基,另一个H原子吸附在Fe原子上形成金属键;第三种吸附发生在O顶位,2个H原子吸附在同一个O原子上,形成H2O分子,此时H2O分子与表面形成物理吸附,H2O分子逃离表面后容易形成氧空位。此外,H2分子在LaFeO3(010)表面还可以发生物理吸附。 |
| 关键词: 密度泛函理论 LaFeO3 表面吸附 H2分子 |
| 基金项目: 国家自然科学基金(No.51562022)、省部共建有色金属先进加工与再利用国家重点实验室开放基金(No.SKLAB02014004)、甘肃省高校基本科研业务费项目(No.05-0342)、兰州市科技项目(No.2011-1-10)、兰州理工大学博士基金(No.BS200901)和NSFC-广东联合基金(第2期)超级计算科学应用研究专项资助。 |
| Abstract: Based on the first principles calculations, the adsorption properties of H2 molecules on LaFeO3 (010) surface are studied after the (010) surface was confirmed as the most stable surface. LaFeO3 (010) surface consists of LaOand FeO2 terminated surfaces, but the adsorption mainly occurs on the FeO2 terminated surface. Due to the surface relaxation, the contact area on the uneven surface lay between surface atoms and Hatoms increased, and resulted into about 2.5% increase of the longitudinal volume of the unit cell surface which is beneficial to the Hatoms diffusion within the crystal. The results indicate that, there are three kinds of chemical adsorption modes of H2 molecules on the surface of LaFeO3 (010): The best adsorption mode is that two Hatoms are adsorbed to the two surface Oatoms respectively, forming two -OHgroups. At this position, the typical covalent bonds between Hand surface Oformed through the orbital hybridization of H1s and O2p. The energy barrier of H2 molecules dissociation is about 1.542 eV, indicating that the dissociative adsorption can be occurred only under certain thermal condition. The second mode is that one Hatom adsorbed on the surface Oatom, forming an -OHgroup, while the other Hatom is adsorbed to the Fe atoms, forming a metal bond. The third mode is that two Hatoms are adsorbed to the same surface Oatom to form H2Omolecules which is physically adsorbed on the surface, but the surface oxygen vacancies can be easily formed after the H2Omolecules escaped from the surface. In addition, H2 molecules also can be physically adsorbed on LaFeO3 (010) surface. |
| Keywords: density functional theory LaFeO3 surface adsorption H2 molecules |
| 投稿时间：2015-11-20 修订日期：2016-04-10 |
| 摘要点击次数: 2208 |
| 全文下载次数: 1885 |
| 陈玉红,潘昌昌,张梅玲,元丽华,张材荣,康龙,罗永春.H2分子在LaFeO3表面吸附的第一性原理研究[J].无机化学学报,2016,32(6):945-953. |
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