New Photoelectron–Valence Electron Interactions Evident in the Photoelectron Spectrum of Gd2O–

原子物理学 化学 原子轨道 激发态 价(化学) 电子 光电发射光谱学 谱线 价电子 离子 原子电子跃迁 电子组态 电子结构 X射线光电子能谱 物理 核磁共振 计算化学 量子力学 有机化学 天文
作者
Jarrett L. Mason,Hassan Harb,Ali Abou Taka,Caleb D. Huizenga,Héctor H. Corzo,Hrant P. Hratchian,Caroline Chick Jarrold
出处
期刊:Journal of Physical Chemistry A [American Chemical Society]
卷期号:125 (45): 9892-9903 被引量:9
标识
DOI:10.1021/acs.jpca.1c07818
摘要

Evidence of strong photoelectron-valence electron (PEVE) interactions has been observed in the anion photoelectron (PE) spectra of several lanthanide suboxide clusters, which are exceptionally complex from an electronic structure standpoint and are strongly correlated systems. The PE spectrum of Gd2O-, which should have relatively simple electronic structure because of its half-filled 4f subshell, exhibits numerous electronic transitions. The electron affinity determined from the spectrum is 0.26 eV. The intensities of transitions to excited states increase relative to the lower-energy states with lower photon energy, which is consistent with shakeup transitions driven by time-dependent electron-neutral interactions. A group of intense spectral features that lie between electron binding energies of 0.7 and 2.3 eV are assigned to transitions involving detachment of an electron from outer-valence σu and σg orbitals that have large Gd 6s contributions. The spectra show parallel transition manifolds in general, which is consistent with detachment from these orbitals. However, several distinct perpendicular transitions are observed adjacent to several of the vertical transitions. A possible explanation invoking interaction between the ejected electron and the high-spin neutral is proposed. Specifically, the angular momentum of electrons ejected from σu or σg orbitals, which is l = 1, can switch to l = 0, 2 with an associated change in the Ms of the remnant neutral, which is spin-orbit coupling between a free electron and the spin of a neutral.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
lina发布了新的文献求助10
1秒前
2秒前
wang完成签到,获得积分10
2秒前
丛玉林发布了新的文献求助10
4秒前
今后应助hkh采纳,获得10
6秒前
8秒前
Rewi_Zhang完成签到,获得积分10
9秒前
感性的靖仇完成签到,获得积分10
10秒前
10秒前
哇哦完成签到,获得积分10
10秒前
Lee完成签到,获得积分10
11秒前
11秒前
善学以致用应助HongJiang采纳,获得10
13秒前
15秒前
一遐完成签到,获得积分10
18秒前
冷静的胜完成签到,获得积分10
18秒前
nn发布了新的文献求助10
19秒前
22秒前
伶俐的雁蓉完成签到,获得积分10
23秒前
23秒前
秋之晨完成签到,获得积分10
23秒前
25秒前
Zwuijl完成签到,获得积分10
25秒前
25秒前
heyan发布了新的文献求助10
27秒前
秋之晨发布了新的文献求助10
27秒前
靓丽衫完成签到 ,获得积分10
31秒前
tuihuo发布了新的文献求助10
31秒前
32秒前
yiersan完成签到,获得积分10
33秒前
hoongyan完成签到 ,获得积分10
35秒前
忧虑的静柏完成签到 ,获得积分10
35秒前
37秒前
科研科研发布了新的文献求助200
37秒前
39秒前
范小雨完成签到,获得积分10
39秒前
39秒前
tuihuo完成签到,获得积分10
40秒前
英俊的铭应助三叔采纳,获得10
41秒前
41秒前
高分求助中
Production Logging: Theoretical and Interpretive Elements 2700
Ophthalmic Equipment Market 1500
Neuromuscular and Electrodiagnostic Medicine Board Review 1000
こんなに痛いのにどうして「なんでもない」と医者にいわれてしまうのでしょうか 510
いちばんやさしい生化学 500
The First Nuclear Era: The Life and Times of a Technological Fixer 500
Unusual formation of 4-diazo-3-nitriminopyrazoles upon acid nitration of pyrazolo[3,4-d][1,2,3]triazoles 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3672729
求助须知:如何正确求助?哪些是违规求助? 3228865
关于积分的说明 9782382
捐赠科研通 2939285
什么是DOI,文献DOI怎么找? 1610797
邀请新用户注册赠送积分活动 760740
科研通“疑难数据库(出版商)”最低求助积分说明 736199