{"title":"Tip carbon encapsulation customizes cationic enrichment and valence stabilization for low K+ acidic CO2 electroreduction","authors":"Zhitong Wang, Dongyu Liu, Chenfeng Xia, Xiaodong Shi, Yansong Zhou, Qiuwen Liu, Jiangtao Huang, Haiyan Wu, Deyu Zhu, Shuyu Zhang, Jing Li, Peilin Deng, Andrey S. Vasenko, Bao Yu Xia, Xinlong Tian","doi":"10.1038/s41467-025-56977-6","DOIUrl":null,"url":null,"abstract":"<p>Acidic electrochemical CO<sub>2</sub> conversion is a promising alternative to overcome the low CO<sub>2</sub> utilization. However, over-reliance on highly concentrated K<sup>+</sup> to inhibit the hydrogen evolution reaction also causes (bi)carbonate precipitation to interfere with catalytic performance. In this work, under the screening and guidance of computational simulations, we present a carbon coated tip-like In<sub>2</sub>O<sub>3</sub> electrocatalyst for stable and efficient acidic CO<sub>2</sub> conversion to synthesize formic acid (HCOOH) with low K<sup>+</sup> concentration. The carbon layer protects the oxidized In species with higher intrinsic activity from reductive corrosion, and also peripherally formulates a tip-induced electric field to regulate the adverse H<sup>+</sup> attraction and desirable K<sup>+</sup> enrichment. In an acidic electrolyte at pH 0.94, only 0.1 M low K<sup>+</sup> is required to achieve a Faradaic efficiency (FE) of 98.9% at 300 mA cm<sup>−2</sup> for HCOOH and a long-time stability of over100 h. By up-scaling the electrode into a 25 cm<sup>2</sup> electrolyzer setup, a total current of 7 A is recorded to sustain a durable HCOOH production of 291.6 mmol L<sup>−1</sup> h<sup>−1</sup>.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"593 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2025-02-19","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/s41467-025-56977-6","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
Acidic electrochemical CO2 conversion is a promising alternative to overcome the low CO2 utilization. However, over-reliance on highly concentrated K+ to inhibit the hydrogen evolution reaction also causes (bi)carbonate precipitation to interfere with catalytic performance. In this work, under the screening and guidance of computational simulations, we present a carbon coated tip-like In2O3 electrocatalyst for stable and efficient acidic CO2 conversion to synthesize formic acid (HCOOH) with low K+ concentration. The carbon layer protects the oxidized In species with higher intrinsic activity from reductive corrosion, and also peripherally formulates a tip-induced electric field to regulate the adverse H+ attraction and desirable K+ enrichment. In an acidic electrolyte at pH 0.94, only 0.1 M low K+ is required to achieve a Faradaic efficiency (FE) of 98.9% at 300 mA cm−2 for HCOOH and a long-time stability of over100 h. By up-scaling the electrode into a 25 cm2 electrolyzer setup, a total current of 7 A is recorded to sustain a durable HCOOH production of 291.6 mmol L−1 h−1.
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.