Yuntao Lei , Wenjuan Zhang , Fenglong Sun , Zhongwei Zhao
{"title":"Molten salt electrodeposition enabling direct and efficient preparation of homogeneous Pb-Li eutectic alloys","authors":"Yuntao Lei , Wenjuan Zhang , Fenglong Sun , Zhongwei Zhao","doi":"10.1016/j.electacta.2025.147416","DOIUrl":null,"url":null,"abstract":"<div><div>Liquid lead-lithium (Pb-Li) alloys are promising tritium breeder materials for nuclear fusion, but conventional high-temperature smelting preparation process remains hampered by low efficiency, compositional segregation, and safety risks from metallic Li feedstocks. Herein, we propose a molten salt electrodeposition strategy using a liquid Pb metal electrode to directly produce Pb-Li alloys. Driven by in-situ alloying and depolarization effects, Li<sup>+</sup> ions from LiCl-KCl molten salts undergo underpotential deposition on the liquid Pb cathode, which enhances current efficiency and reduces electrolysis energy consumption. Homogeneous Pb-Li alloys are stably obtained across a wide range of conditions, including Li content (10–35 at%), current density (100–500 mA·cm⁻²), and temperature (400–550 °C), with current efficiencies consistently maintained above 80 %. A kilogram-scale experiment validates that potential-feedback galvanostatic electrodeposition enables precise synthesis of Pb-Li eutectic alloys with an average Li content of 17.10 ± 0.80 at %, reducing carbon emissions by 83.9 kg CO₂e·t⁻¹-alloy and lowering production costs by $143.6 per ton alloy compared to smelting. This approach exhibits stability, sustainability, and scalability for precisely fabricating homogeneous Pb-Li and analogous Li-based alloys.</div></div>","PeriodicalId":305,"journal":{"name":"Electrochimica Acta","volume":"542 ","pages":"Article 147416"},"PeriodicalIF":5.6000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochimica Acta","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0013468625017736","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Liquid lead-lithium (Pb-Li) alloys are promising tritium breeder materials for nuclear fusion, but conventional high-temperature smelting preparation process remains hampered by low efficiency, compositional segregation, and safety risks from metallic Li feedstocks. Herein, we propose a molten salt electrodeposition strategy using a liquid Pb metal electrode to directly produce Pb-Li alloys. Driven by in-situ alloying and depolarization effects, Li+ ions from LiCl-KCl molten salts undergo underpotential deposition on the liquid Pb cathode, which enhances current efficiency and reduces electrolysis energy consumption. Homogeneous Pb-Li alloys are stably obtained across a wide range of conditions, including Li content (10–35 at%), current density (100–500 mA·cm⁻²), and temperature (400–550 °C), with current efficiencies consistently maintained above 80 %. A kilogram-scale experiment validates that potential-feedback galvanostatic electrodeposition enables precise synthesis of Pb-Li eutectic alloys with an average Li content of 17.10 ± 0.80 at %, reducing carbon emissions by 83.9 kg CO₂e·t⁻¹-alloy and lowering production costs by $143.6 per ton alloy compared to smelting. This approach exhibits stability, sustainability, and scalability for precisely fabricating homogeneous Pb-Li and analogous Li-based alloys.
期刊介绍:
Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.