• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

氧分子自旋禁阻光解离后单重态氧的转动分布与成像

Rotational Distributions and Imaging of Singlet O Following Spin-Forbidden Photodissociation of O.

作者信息

Aardema Megan N, Fast Megan, Meas Benjamen, North Simon W

机构信息

Department of Chemistry, Texas A&M University, College Station, Texas 77842, United States.

出版信息

J Phys Chem A. 2023 Aug 31;127(34):7101-7114. doi: 10.1021/acs.jpca.3c02736. Epub 2023 Aug 4.

DOI:10.1021/acs.jpca.3c02736
PMID:37540577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10863062/
Abstract

We report REMPI spectra and velocity-mapped ion images of the O(Δ) and (Σ) fragments arising from the spin-forbidden photodissociation of O near 320 and 330 nm. The O(Δ, v = 0) REMPI spectrum following a 320 nm dissociation shows enhanced peak intensity for the odd rotational states relative to the even states, which is the opposite of the trend observed by Gunthardt et al. ( 2019, 151, 224302) for spin-allowed dissociation at 266 nm but is consistent with the couplings between the B state and A' and A″ states calculated by Grebenshchikov and Rosenwaks ( 2010, 114, 9809-9819). There are no significant differences between the ion image angular distributions of fragments in odd and even rotational states, which indicates a cold distribution of O and supports the explanation that the alternation in peak intensities results from a difference in the couplings. Quantitative analysis of the image angular distributions was limited due to the single laser polarization geometry accessible in one-color experiments. Radial distributions of the 320 nm images indicate a broad rotational distribution, evidenced in bimodal speed distributions with peaks corresponding to both high ( = 35-43) and low ( = 17-20) rotational states. The REMPI spectrum of O(Δ) near 330 nm was collected, and while quantitative population analysis is difficult because of the perturbed resonant state, the spectrum clearly supports a broad rotational distribution as well, consistent with the images collected at 320 nm. A 2D-REMPI spectrum was collected following dissociation of O near 330 nm, which showed evidence of contributions from O fragments in both the Δ and Σ states. The rotational distribution for the O(Σ, v = 0) product peaks at = 32 and is narrower than that of the O(Δ) fragment, consistent with distributions reported by O'Keeffe et al. at longer dissociation wavelengths ( , 117, 8705-8709). At smaller radii in the 2D-REMPI spectrum, there is additional signal assigned to v = 1-4 of O(Σ), with rotational distributions similar to v = 0. The vibrational distribution of the O(Σ) fragment peaks at v = 0, with populations monotonically decreasing with increasing vibrational state. Ion image angular distributions of the O(Σ) fragment and the corresponding anisotropy parameters are also reported.

摘要

我们报告了在320和330 nm附近O的自旋禁阻光解离产生的O(Δ)和(Σ)碎片的共振增强多光子电离(REMPI)光谱和速度映射离子图像。在320 nm解离后得到的O(Δ, v = 0) REMPI光谱显示,相对于偶数转动态,奇数转动态的峰强度增强,这与Gunthardt等人(2019, 151, 224302)在266 nm自旋允许解离时观察到的趋势相反,但与Grebenshchikov和Rosenwaks(2010, 114, 9809 - 9819)计算的B态与A'和A″态之间的耦合一致。奇数和偶数转动态碎片的离子图像角分布没有显著差异,这表明O的分布是冷分布,并支持峰强度交替是由耦合差异导致的解释。由于单色实验中可获得的单一激光偏振几何结构,对图像角分布的定量分析受到限制。320 nm图像的径向分布表明存在广泛的转动分布,这在双峰速度分布中得到证明,其峰值分别对应高( = 35 - 43)和低( = 17 - 20)转动态。收集了330 nm附近O(Δ)的REMPI光谱,虽然由于共振态受到扰动,定量布居分析困难,但该光谱也清楚地支持了广泛的转动分布,这与在320 nm收集的图像一致。在330 nm附近O解离后收集了二维REMPI光谱,这表明在Δ和Σ态的O碎片都有贡献。O(Σ, v = 0)产物的转动分布在 = 32处达到峰值,且比O(Δ)碎片的转动分布更窄,这与O'Keeffe等人在更长解离波长下报道的分布一致(, 117, 8705 - 8709)。在二维REMPI光谱中较小半径处,有额外的信号归属于O(Σ)的v = 1 - 至4,其转动分布与v = 0相似。O(Σ)碎片的振动分布在v = 0处达到峰值,布居数随着振动态的增加单调减少。还报告了O(Σ)碎片的离子图像角分布和相应的各向异性参数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/41afd9ed2163/jp3c02736_0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/681aa1ea0c5a/jp3c02736_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/5a3c4f6a9815/jp3c02736_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/8356da9c9e29/jp3c02736_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/a1e88b11491a/jp3c02736_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/a8f1939cb519/jp3c02736_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/14bae929da2b/jp3c02736_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/63f7a1c59951/jp3c02736_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/a144ad1c5625/jp3c02736_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/5d3aaa1ef10d/jp3c02736_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/b8a848afe2e4/jp3c02736_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/d6fb4af057db/jp3c02736_0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/f35ffbb7ae9f/jp3c02736_0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/51f8d8b8d549/jp3c02736_0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/41afd9ed2163/jp3c02736_0014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/681aa1ea0c5a/jp3c02736_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/5a3c4f6a9815/jp3c02736_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/8356da9c9e29/jp3c02736_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/a1e88b11491a/jp3c02736_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/a8f1939cb519/jp3c02736_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/14bae929da2b/jp3c02736_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/63f7a1c59951/jp3c02736_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/a144ad1c5625/jp3c02736_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/5d3aaa1ef10d/jp3c02736_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/b8a848afe2e4/jp3c02736_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/d6fb4af057db/jp3c02736_0011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/f35ffbb7ae9f/jp3c02736_0012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/51f8d8b8d549/jp3c02736_0013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1489/10863062/41afd9ed2163/jp3c02736_0014.jpg

相似文献

1
Rotational Distributions and Imaging of Singlet O Following Spin-Forbidden Photodissociation of O.氧分子自旋禁阻光解离后单重态氧的转动分布与成像
J Phys Chem A. 2023 Aug 31;127(34):7101-7114. doi: 10.1021/acs.jpca.3c02736. Epub 2023 Aug 4.
2
Imaging study of O3 photodissociation in the Huggins band.
J Chem Phys. 2024 Sep 28;161(12). doi: 10.1063/5.0230902.
3
Ozone Photodissociation in the Singlet Channel at 226 nm.226纳米处单重态通道中的臭氧光解离
J Phys Chem A. 2022 Oct 6;126(39):6898-6907. doi: 10.1021/acs.jpca.2c04832. Epub 2022 Sep 21.
4
Nascent O ( Δ, = 0, 1) rotational distributions from the photodissociation of jet-cooled O in the Hartley band.初生 O(Δ,=0,1)的转动分布来自哈特利带中喷射冷却 O 的光解。
J Chem Phys. 2018 Oct 7;149(13):134309. doi: 10.1063/1.5051540.
5
Evidence for lambda doublet propensity in the UV photodissociation of ozone.证据表明,在臭氧的紫外光解过程中存在双原子氧倾向。
J Chem Phys. 2019 Dec 14;151(22):224302. doi: 10.1063/1.5131504.
6
UV Photodissociation Dynamics of the CH3CHOO Criegee Intermediate: Action Spectroscopy and Velocity Map Imaging of O-Atom Products.CH3CHOO 克里吉中间体的紫外光解离动力学:O 原子产物的作用光谱和速度映射成像
J Phys Chem A. 2015 Jul 30;119(30):8328-37. doi: 10.1021/acs.jpca.5b05352. Epub 2015 Jul 20.
7
Photodissociation of ozone from 321 to 329 nm: the relative yields of O(3P2) with O2(X 3Σg(-)), O2(a 1Δg) and O2(b 1Σg(+)).321 至 329nm 光解臭氧:O(3P2)与 O2(X 3Σg(-))、O2(a 1Δg)和 O2(b 1Σg(+))的相对产率。
J Phys Chem A. 2013 Nov 21;117(46):12011-9. doi: 10.1021/jp4041088. Epub 2013 Aug 23.
8
Photodissociation of singlet oxygen in the UV region.在紫外区域单线态氧的光解。
Phys Chem Chem Phys. 2014 Feb 21;16(7):3305-16. doi: 10.1039/c3cp54696a.
9
Speed dependent rotational angular momentum polarization of the O2 (a 1Deltag) fragment following ozone photolysis in the wavelength range 248-265 nm.在248 - 265纳米波长范围内臭氧光解后,O2(a 1Deltag)碎片的速度相关旋转角动量极化。
J Chem Phys. 2007 Sep 21;127(11):114308. doi: 10.1063/1.2775453.
10
Photodissociation dynamics of OCS near 214 nm using ion imaging.利用离子成像技术研究OCS在214纳米附近的光解离动力学。
J Chem Phys. 2016 Jul 14;145(2):024310. doi: 10.1063/1.4955189.

本文引用的文献

1
Ozone Photodissociation in the Singlet Channel at 226 nm.226纳米处单重态通道中的臭氧光解离
J Phys Chem A. 2022 Oct 6;126(39):6898-6907. doi: 10.1021/acs.jpca.2c04832. Epub 2022 Sep 21.
2
Origin of the "odd" behavior in the ultraviolet photochemistry of ozone.臭氧紫外光化学反应中“奇怪”行为的起源。
Proc Natl Acad Sci U S A. 2020 Sep 1;117(35):21065-21069. doi: 10.1073/pnas.2006070117. Epub 2020 Aug 12.
3
Evidence for lambda doublet propensity in the UV photodissociation of ozone.证据表明,在臭氧的紫外光解过程中存在双原子氧倾向。
J Chem Phys. 2019 Dec 14;151(22):224302. doi: 10.1063/1.5131504.
4
Nascent O ( Δ, = 0, 1) rotational distributions from the photodissociation of jet-cooled O in the Hartley band.初生 O(Δ,=0,1)的转动分布来自哈特利带中喷射冷却 O 的光解。
J Chem Phys. 2018 Oct 7;149(13):134309. doi: 10.1063/1.5051540.
5
The energy dependence of CO(v,J) produced from HCO via the transition state, roaming, and triple fragmentation channels.通过过渡态、漫游和三重碎裂通道,从 HCO 产生的 CO(v,J)的能量依赖性。
J Chem Phys. 2017 Jul 7;147(1):013935. doi: 10.1063/1.4983138.
6
A method of extracting speed-dependent vector correlations from 2 + 1 REMPI ion images.一种从 2+1 REMPI 离子图像中提取速度相关矢量关联的方法。
J Chem Phys. 2017 Jul 7;147(1):013947. doi: 10.1063/1.4985704.
7
Signatures of a conical intersection in photofragment distributions and absorption spectra: photodissociation in the Hartley band of ozone.光解离碎片分布和吸收光谱中锥形交叉的特征:臭氧哈特利带中的光解离
J Chem Phys. 2014 Aug 21;141(7):074311. doi: 10.1063/1.4892919.
8
Photodissociation of ozone from 321 to 329 nm: the relative yields of O(3P2) with O2(X 3Σg(-)), O2(a 1Δg) and O2(b 1Σg(+)).321 至 329nm 光解臭氧:O(3P2)与 O2(X 3Σg(-))、O2(a 1Δg)和 O2(b 1Σg(+))的相对产率。
J Phys Chem A. 2013 Nov 21;117(46):12011-9. doi: 10.1021/jp4041088. Epub 2013 Aug 23.
9
Photodissociation dynamics of tert-butylnitrite following excitation to the S1 and S2 states. A study by velocity-map ion-imaging and 3D-REMPI spectroscopy.叔丁基亚硝酯在 S1 和 S2 态激发后的光解动力学。通过速度映射离子成像和 3D-REMPI 光谱学研究。
Phys Chem Chem Phys. 2012 May 21;14(19):7076-89. doi: 10.1039/c2cp40349h. Epub 2012 Apr 10.
10
Ion imaging study of NO3 radical photodissociation dynamics: characterization of multiple reaction pathways.离子成像研究 NO3 自由基光解动力学:多种反应途径的特征。
J Phys Chem A. 2011 Apr 21;115(15):3218-26. doi: 10.1021/jp200110e. Epub 2011 Mar 29.