{"title":"在高压电子能谱中利用奥杰跃迁确定铜的氧化态","authors":"","doi":"10.1016/j.susc.2024.122565","DOIUrl":null,"url":null,"abstract":"<div><p>Accurate discrimination between metallic copper (Cu<sup>0</sup>) and cuprous oxide (Cu<sub>2</sub>O, Cu<sup>+</sup>) in electron spectroscopy commonly relies on the Auger electron spectroscopy (AES) Cu L<sub>3</sub>M<sub>4,5</sub>M<sub>4,5</sub> transitions, as the X-ray photoelectron spectroscopy (XPS) Cu core-levels do not provide large enough binding energy shifts. The kinetic energy of the AES Cu L<sub>3</sub>M<sub>4,5</sub>M<sub>4,5</sub> electrons is ∼917 eV, which leaves the AES electron susceptible for efficient scattering in the gas phase and attenuation of the signal above near-ambient pressure conditions. To study copper-based materials at higher pressures, e.g., the active state of a catalyst, Auger transitions providing electrons with higher kinetic energies are needed.</p><p>This study focuses on AES transitions involving the Cu K-shell (1s electrons) that exhibit discernible kinetic energy shifts between the oxidation states of Cu. It is shown that the AES Cu KL<sub>2</sub>M<sub>4,5</sub> transition, with kinetic energy of ∼7936 eV, provides a large enough kinetic energy shift between metallic copper and Cu<sub>2</sub>O. AES signal is demonstrated in an ambient of 150 mbar CO<sub>2</sub>.</p></div>","PeriodicalId":22100,"journal":{"name":"Surface Science","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2024-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S003960282400116X/pdfft?md5=4fdbf89520066107d67767248dbe3449&pid=1-s2.0-S003960282400116X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Using Auger transitions as a route to determine the oxidation state of copper in high-pressure electron spectroscopy\",\"authors\":\"\",\"doi\":\"10.1016/j.susc.2024.122565\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Accurate discrimination between metallic copper (Cu<sup>0</sup>) and cuprous oxide (Cu<sub>2</sub>O, Cu<sup>+</sup>) in electron spectroscopy commonly relies on the Auger electron spectroscopy (AES) Cu L<sub>3</sub>M<sub>4,5</sub>M<sub>4,5</sub> transitions, as the X-ray photoelectron spectroscopy (XPS) Cu core-levels do not provide large enough binding energy shifts. The kinetic energy of the AES Cu L<sub>3</sub>M<sub>4,5</sub>M<sub>4,5</sub> electrons is ∼917 eV, which leaves the AES electron susceptible for efficient scattering in the gas phase and attenuation of the signal above near-ambient pressure conditions. To study copper-based materials at higher pressures, e.g., the active state of a catalyst, Auger transitions providing electrons with higher kinetic energies are needed.</p><p>This study focuses on AES transitions involving the Cu K-shell (1s electrons) that exhibit discernible kinetic energy shifts between the oxidation states of Cu. It is shown that the AES Cu KL<sub>2</sub>M<sub>4,5</sub> transition, with kinetic energy of ∼7936 eV, provides a large enough kinetic energy shift between metallic copper and Cu<sub>2</sub>O. AES signal is demonstrated in an ambient of 150 mbar CO<sub>2</sub>.</p></div>\",\"PeriodicalId\":22100,\"journal\":{\"name\":\"Surface Science\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-07-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S003960282400116X/pdfft?md5=4fdbf89520066107d67767248dbe3449&pid=1-s2.0-S003960282400116X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Surface Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S003960282400116X\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Surface Science","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S003960282400116X","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
由于 X 射线光电子能谱 (XPS) 中的铜核级不能提供足够大的结合能位移,因此在电子能谱中准确区分金属铜 (Cu0) 和氧化亚铜 (Cu2O, Cu+)通常依赖于奥杰电子能谱 (AES) 中的 Cu L3M4,5M4,5 转变。AES Cu L3M4,5M4,5 电子的动能为 ∼917 eV,这使得 AES 电子容易在气相中发生有效散射,在近环境压力条件下信号会衰减。为了在更高压力下研究铜基材料,例如催化剂的活性状态,需要奥杰跃迁提供动能更高的电子。本研究重点关注涉及铜 K 壳(1s 电子)的 AES 跃迁,这些电子在铜的氧化态之间表现出明显的动能转移。研究表明,动能为 ∼7936 eV 的 AES Cu KL2M4,5 转变在金属铜和 Cu2O 之间提供了足够大的动能转移。AES 信号在 150 毫巴二氧化碳环境中得到了证实。
Using Auger transitions as a route to determine the oxidation state of copper in high-pressure electron spectroscopy
Accurate discrimination between metallic copper (Cu0) and cuprous oxide (Cu2O, Cu+) in electron spectroscopy commonly relies on the Auger electron spectroscopy (AES) Cu L3M4,5M4,5 transitions, as the X-ray photoelectron spectroscopy (XPS) Cu core-levels do not provide large enough binding energy shifts. The kinetic energy of the AES Cu L3M4,5M4,5 electrons is ∼917 eV, which leaves the AES electron susceptible for efficient scattering in the gas phase and attenuation of the signal above near-ambient pressure conditions. To study copper-based materials at higher pressures, e.g., the active state of a catalyst, Auger transitions providing electrons with higher kinetic energies are needed.
This study focuses on AES transitions involving the Cu K-shell (1s electrons) that exhibit discernible kinetic energy shifts between the oxidation states of Cu. It is shown that the AES Cu KL2M4,5 transition, with kinetic energy of ∼7936 eV, provides a large enough kinetic energy shift between metallic copper and Cu2O. AES signal is demonstrated in an ambient of 150 mbar CO2.
期刊介绍:
Surface Science is devoted to elucidating the fundamental aspects of chemistry and physics occurring at a wide range of surfaces and interfaces and to disseminating this knowledge fast. The journal welcomes a broad spectrum of topics, including but not limited to:
• model systems (e.g. in Ultra High Vacuum) under well-controlled reactive conditions
• nanoscale science and engineering, including manipulation of matter at the atomic/molecular scale and assembly phenomena
• reactivity of surfaces as related to various applied areas including heterogeneous catalysis, chemistry at electrified interfaces, and semiconductors functionalization
• phenomena at interfaces relevant to energy storage and conversion, and fuels production and utilization
• surface reactivity for environmental protection and pollution remediation
• interactions at surfaces of soft matter, including polymers and biomaterials.
Both experimental and theoretical work, including modeling, is within the scope of the journal. Work published in Surface Science reaches a wide readership, from chemistry and physics to biology and materials science and engineering, providing an excellent forum for cross-fertilization of ideas and broad dissemination of scientific discoveries.