Xiaotong Li,Kainan Gao,Mingliang Qu,Nanhui Li,Xiangzhou Lv,Xiuju Wu,Qingyang Lin,Hao Bin Wu
{"title":"Membrane-free CO2 electrolyzer design for economically efficient formic acid electro-synthesis.","authors":"Xiaotong Li,Kainan Gao,Mingliang Qu,Nanhui Li,Xiangzhou Lv,Xiuju Wu,Qingyang Lin,Hao Bin Wu","doi":"10.1038/s41467-025-64306-0","DOIUrl":null,"url":null,"abstract":"Reducing the electrical energy consumption for formic acid electro-synthesis is indispensable for advancing its industrial implementation. In a conventional CO2 electrolyzer, most input electrical energy is consumed by the unprofitable anodic oxygen evolution reaction (OER) and ohmic drop. Electrolyzer engineering provides a promising platform to boost electrical energy utilization efficiency beyond catalyst optimization. Herein, we demonstrate a membrane-free CO2 electrolyzer design that pairs electrochemical CO2 reduction (CO2R) with an all-liquid-phase anodic reaction, enabling dual production of formate at both electrodes with significantly reduced cell voltage. The optimized design exhibits the lowest electrical energy consumption (< 310 kJ mol-1formate) at cell voltages below 2.7 V across a current density range of 0.05-0.4 A cm-2. This cell also maintains stable operation at 2.25 V for 313 h with a < 20 % increase in electrical energy consumption. Systematic techno-economic analysis (TEA) evaluates the economic viability of this design for formic acid electro-synthesis, revealing a potential roadmap towards low-cost formic acid production. This strategy provides guidelines for CO2R electrolyzer engineering toward energy-efficient, economically viable production of valuable chemicals.","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"20 1","pages":"9237"},"PeriodicalIF":15.7000,"publicationDate":"2025-10-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-64306-0","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Reducing the electrical energy consumption for formic acid electro-synthesis is indispensable for advancing its industrial implementation. In a conventional CO2 electrolyzer, most input electrical energy is consumed by the unprofitable anodic oxygen evolution reaction (OER) and ohmic drop. Electrolyzer engineering provides a promising platform to boost electrical energy utilization efficiency beyond catalyst optimization. Herein, we demonstrate a membrane-free CO2 electrolyzer design that pairs electrochemical CO2 reduction (CO2R) with an all-liquid-phase anodic reaction, enabling dual production of formate at both electrodes with significantly reduced cell voltage. The optimized design exhibits the lowest electrical energy consumption (< 310 kJ mol-1formate) at cell voltages below 2.7 V across a current density range of 0.05-0.4 A cm-2. This cell also maintains stable operation at 2.25 V for 313 h with a < 20 % increase in electrical energy consumption. Systematic techno-economic analysis (TEA) evaluates the economic viability of this design for formic acid electro-synthesis, revealing a potential roadmap towards low-cost formic acid production. This strategy provides guidelines for CO2R electrolyzer engineering toward energy-efficient, economically viable production of valuable chemicals.
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.