Protective In Situ Oxide Layer Formation at a Nonconsumable Iron Anode for Molten Salt Carbon Dioxide Electrolysis

IF 5.2 3区 工程技术 Q2 ENERGY & FUELS
Jessica Allen*, Mitchell Hunt and Simin Moradmand, 
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Abstract

In this work, the apparent stability of an iron anode undergoing oxygen evolution in a ternary molten carbonate salt eutectic ((Li/Na/K)2CO3) is investigated at 600 °C. In this system, carbon is produced at the cathode for the overall transformation of carbon dioxide to high-value carbon materials. The high variability in the initial iron electrode electrochemical oxidation response at low potentials is shown to originate from the electrochemical sensitivity toward surface iron oxides, which form at the iron electrode surface under the operational conditions. These result from the interaction with small concentrations of oxygen in the cell gas environment (<3 vol %), chemical reaction of oxides, and iron with the carbonate salts present with both direct and indirect (vapor phase) contact, and electrochemical surface oxidation. Despite the demonstrated high susceptibility of iron toward oxidative corrosion under these conditions, when the partially oxidized iron electrode is polarized to undergo oxygen gas evolution, apparent stability is observed. The corrosion rate for iron electrodes operating under a current density of 300 mA·cm–2 is estimated to be 3.18–7.68 mm·year–1, an acceptable range for nonconsumable anodes. The unexpected stability of the iron electrode is ascribed to the formation of specific lithium ferrite species. LiFe5O8 is specifically confirmed to be formed, which is suggested here to result from the interaction of evolved oxygen gas (O2) with oxide (O2–) present in the carbonate melt to form a highly oxidizing species, peroxide (O22–). LiFe5O8 is suggested here to form from the interaction of peroxide, lithium salts, and iron species, demonstrating a novel low-temperature pathway for the formation of this species. The intrinsic oxide species activity and reasonable electrical conductivity of lithium ferrite result in a stable and active final anode surface, which does not appear to rely on careful pretreatment prior to sustained oxygen evolution.

熔盐二氧化碳电解用非消耗性铁阳极保护原位氧化层的形成
在这项工作中,研究了在三元熔融碳酸盐共晶((Li/Na/K)2CO3)中经历析氧的铁阳极在600℃下的表观稳定性。在这个系统中,碳在阴极产生,将二氧化碳全面转化为高价值的碳材料。低电势下铁电极初始电化学氧化响应的高变异性源于铁电极在工作条件下对表面氧化铁的电化学敏感性。这是由于与电池气体环境中的低浓度氧气(3 vol %)的相互作用,氧化物的化学反应,以及铁与碳酸盐的直接和间接(气相)接触,以及电化学表面氧化。尽管在这些条件下铁对氧化腐蚀表现出很高的敏感性,但当部分氧化的铁电极极化以进行氧气释放时,观察到明显的稳定性。在300 mA·cm-2电流密度下,铁电极的腐蚀速率估计为3.18-7.68 mm·年- 1,对于非消耗性阳极来说,这是一个可以接受的范围。铁电极意想不到的稳定性归因于形成特定的锂铁氧体物种。LiFe5O8的形成得到了明确的证实,这是由碳酸盐熔体中演化出的氧气(O2)与氧化物(O2 -)相互作用产生的,形成了一种高度氧化的物质——过氧化物(O22 -)。本文认为LiFe5O8是由过氧化物、锂盐和铁种相互作用形成的,证明了这种铁种形成的一种新的低温途径。铁酸锂固有的氧化物活性和合理的电导率导致最终阳极表面稳定而活跃,这似乎不依赖于持续析氧之前的仔细预处理。
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来源期刊
Energy & Fuels
Energy & Fuels 工程技术-工程:化工
CiteScore
9.20
自引率
13.20%
发文量
1101
审稿时长
2.1 months
期刊介绍: Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.
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