{"title":"Hydrogen egress from palladium surfaces: A microelectrode-based investigation","authors":"S. Zhang , K. Nairn , M. Musameh , S. Thomas","doi":"10.1016/j.jelechem.2023.117690","DOIUrl":null,"url":null,"abstract":"<div><p>Atomic hydrogen could participate in multiple electrochemical reactions during egress from Palladium (Pd) into aqueous environments. Possible reactions include hydrogen recombination to form H<sub>2</sub>, the oxygen reduction reaction (ORR) and “hydrogen ionisation” to form H<sup>+</sup>. Here, bulk measurements and microelectrode-based methods were used to mechanistically investigate such reactions occurring during hydrogen egress from Pd. Significant ORR was detected on hydrogen-charged Pd (Pd-H) surfaces, when using a Platinum (Pt) microelectrode (ME) in the redox competition mode. However, minor hydrogen recombination was also detected while using the Pt ME in the sample generation-tip collection (SG-TC) mode. Hydrogen ionisation is observed to occur when Pd (H) is anodically polarised. These reactions can all be linked to the highly negative equilibrium potential of the atomic H/H<sup>+</sup> redox couple. Atomic hydrogen being a strong reducing agent thus tends to efficiently reduce various oxidants in solution resulting in different products, under varying conditions.</p></div>","PeriodicalId":50545,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"946 ","pages":"Article 117690"},"PeriodicalIF":4.5000,"publicationDate":"2023-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665723005507","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/8/2 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Chemical Engineering","Score":null,"Total":0}
引用次数: 0
Abstract
Atomic hydrogen could participate in multiple electrochemical reactions during egress from Palladium (Pd) into aqueous environments. Possible reactions include hydrogen recombination to form H2, the oxygen reduction reaction (ORR) and “hydrogen ionisation” to form H+. Here, bulk measurements and microelectrode-based methods were used to mechanistically investigate such reactions occurring during hydrogen egress from Pd. Significant ORR was detected on hydrogen-charged Pd (Pd-H) surfaces, when using a Platinum (Pt) microelectrode (ME) in the redox competition mode. However, minor hydrogen recombination was also detected while using the Pt ME in the sample generation-tip collection (SG-TC) mode. Hydrogen ionisation is observed to occur when Pd (H) is anodically polarised. These reactions can all be linked to the highly negative equilibrium potential of the atomic H/H+ redox couple. Atomic hydrogen being a strong reducing agent thus tends to efficiently reduce various oxidants in solution resulting in different products, under varying conditions.
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.