Niklas H. Deissler , Valentin Vinci , Jon Bjarke Valbæk Mygind , Xianbiao Fu , Shaofeng Li , Jakob Kibsgaard , Jakub Drnec , Ib Chorkendorff
{"title":"一种用于操作同步加速器实验的新型3d打印电化学电池","authors":"Niklas H. Deissler , Valentin Vinci , Jon Bjarke Valbæk Mygind , Xianbiao Fu , Shaofeng Li , Jakob Kibsgaard , Jakub Drnec , Ib Chorkendorff","doi":"10.1016/j.nxener.2025.100279","DOIUrl":null,"url":null,"abstract":"<div><div>Electrochemical processes are often accompanied by significant transformations at the electrode-electrolyte interface, such as the formation of a solid electrolyte interphase or surface reconstruction. Studying these dynamic changes requires operando characterization techniques to overcome the limitations of ex-situ methods. Here, we present a novel, versatile electrochemical cell optimized for operando synchrotron X-ray studies of the lithium-mediated nitrogen reduction reaction. The cell integrates a single-crystal working electrode with a gas diffusion counter electrode, enabling enhanced faradaic efficiencies (FEs) and operando measurements under conditions that closely resemble scalable flow systems. The cell design improves N₂ availability and suppresses undesirable counter electrode reactions through the hydrogen oxidation reaction, achieving FEs of up to 37% for ammonia production. Fabrication by 3D-printing polyether ether ketone allows for complex electrolyte flow geometries while maintaining minimal X-ray background interference, critical for X-ray-based techniques. The combination of single-crystal electrodes and optimized flow conditions offers a promising platform for investigating fundamental electrochemical processes under realistic and scalable conditions.</div></div>","PeriodicalId":100957,"journal":{"name":"Next Energy","volume":"8 ","pages":"Article 100279"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A novel 3D-printed electrochemical cell for operando synchrotron experiments\",\"authors\":\"Niklas H. Deissler , Valentin Vinci , Jon Bjarke Valbæk Mygind , Xianbiao Fu , Shaofeng Li , Jakob Kibsgaard , Jakub Drnec , Ib Chorkendorff\",\"doi\":\"10.1016/j.nxener.2025.100279\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Electrochemical processes are often accompanied by significant transformations at the electrode-electrolyte interface, such as the formation of a solid electrolyte interphase or surface reconstruction. Studying these dynamic changes requires operando characterization techniques to overcome the limitations of ex-situ methods. Here, we present a novel, versatile electrochemical cell optimized for operando synchrotron X-ray studies of the lithium-mediated nitrogen reduction reaction. The cell integrates a single-crystal working electrode with a gas diffusion counter electrode, enabling enhanced faradaic efficiencies (FEs) and operando measurements under conditions that closely resemble scalable flow systems. The cell design improves N₂ availability and suppresses undesirable counter electrode reactions through the hydrogen oxidation reaction, achieving FEs of up to 37% for ammonia production. Fabrication by 3D-printing polyether ether ketone allows for complex electrolyte flow geometries while maintaining minimal X-ray background interference, critical for X-ray-based techniques. The combination of single-crystal electrodes and optimized flow conditions offers a promising platform for investigating fundamental electrochemical processes under realistic and scalable conditions.</div></div>\",\"PeriodicalId\":100957,\"journal\":{\"name\":\"Next Energy\",\"volume\":\"8 \",\"pages\":\"Article 100279\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-04-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Next Energy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2949821X25000420\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Energy","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949821X25000420","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A novel 3D-printed electrochemical cell for operando synchrotron experiments
Electrochemical processes are often accompanied by significant transformations at the electrode-electrolyte interface, such as the formation of a solid electrolyte interphase or surface reconstruction. Studying these dynamic changes requires operando characterization techniques to overcome the limitations of ex-situ methods. Here, we present a novel, versatile electrochemical cell optimized for operando synchrotron X-ray studies of the lithium-mediated nitrogen reduction reaction. The cell integrates a single-crystal working electrode with a gas diffusion counter electrode, enabling enhanced faradaic efficiencies (FEs) and operando measurements under conditions that closely resemble scalable flow systems. The cell design improves N₂ availability and suppresses undesirable counter electrode reactions through the hydrogen oxidation reaction, achieving FEs of up to 37% for ammonia production. Fabrication by 3D-printing polyether ether ketone allows for complex electrolyte flow geometries while maintaining minimal X-ray background interference, critical for X-ray-based techniques. The combination of single-crystal electrodes and optimized flow conditions offers a promising platform for investigating fundamental electrochemical processes under realistic and scalable conditions.