A Tunable Strategy for Continuous Production of Electrolyte-Free Formic Acid and Sodium Formate in a Solid-State-Electrolyte Based Electrocatalytic CO2 Reduction System.

IF 14.1 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jinrui Guo, Wenqiang Qi, Rongrong Mo, Feiyi Yuan, Lin Wang, Yongmei Li
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引用次数: 0

Abstract

Electrocatalytic CO2 reduction reaction (CO2RR) based on solid-state-electrolyte (SSE) reactors can efficiently convert CO2 to electrolyte-free formic acid (HCOOH) solution, thereby circumventing energy-intensive downstream separation processes and further fostering the advancement of carbon-neutral technologies. However, the absence of alkali metal cations in the SSE-based CO2RR process at the cathode poses a challenge, constraining the performance and stability of CO2RR and exacerbating the hydrogen evolution side reaction. Herein, a novel strategy for the tunable production of both electrolyte-free HCOOH and sodium formate (HCOONa) solution through the regulation of anolyte composition in an SSE-based cell is reported. Employing this strategy, the continuous generation of a ≈0.27 m electrolyte-free HCOONa solution and ≈0.22 m electrolyte-free HCOOH solution with extended stabilities of 300 and 200 h, respectively is achieved. More importantly, the introduction of sodium ions resulted in a reduction of cell voltage by ≈1000 mV and further enhances the stability of the cell. In situ infrared spectroscopy and density functional theory calculations reveal that GB-Bi requires a lower applied potential for formate production, owing to its stronger binding energy to the key intermediate OCHO* compared to Bi. Finally, a techno-economic analysis indicates that this strategy for HCOONa solution production possesses excellent economic viability.

固态电解液电催化CO2还原系统中连续生产无电解甲酸和甲酸钠的可调策略。
基于固态电解质(SSE)反应器的电催化CO2还原反应(CO2RR)可以有效地将CO2转化为无电解质甲酸(HCOOH)溶液,从而避免了能源密集型的下游分离过程,进一步促进了碳中和技术的发展。然而,在sse基CO2RR工艺的阴极处缺少碱金属阳离子是一个挑战,限制了CO2RR的性能和稳定性,加剧了析氢副反应。本文报道了一种在sse基电池中通过调节阳极液组成来可调生产无电解质HCOOH和甲酸钠(hcooa)溶液的新策略。采用该策略,可连续生成≈0.27 m无电解质hcooa溶液和≈0.22 m无电解质HCOOH溶液,稳定性分别延长至300和200 h。更重要的是,钠离子的引入使电池电压降低了约1000 mV,进一步提高了电池的稳定性。原位红外光谱和密度泛函理论计算表明,由于与Bi相比,GB-Bi对关键中间体OCHO*的结合能更强,因此需要更低的甲酸生产应用潜力。最后,技术经济分析表明,该策略对HCOONa溶液生产具有良好的经济可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Science
Advanced Science CHEMISTRY, MULTIDISCIPLINARYNANOSCIENCE &-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
18.90
自引率
2.60%
发文量
1602
审稿时长
1.9 months
期刊介绍: Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.
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