原位阴极极化法研究sr2feom0.6 ni0.4 o6的析出过程

Leonardo Duranti, Andrea Felli, Marcello Marelli, Melodj Dosa, Elisabetta Di Bartolomeo, Marco Piumetti, Marta Boaro
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In the last decade, simple perovskite (ABO 3 ) and double perovskite (A 2 BBʹO 6 ) oxide have been proved to be a valuable alternative to cermet SOC electrodes, thanks to their relative ease of functionalization via doping and exsolution and their mixed ionic-electron conduction 4-6 . Exsolution process is strongly dependent on the type of metal and perovskite and on methodology adopted to induce the reduction 7 . Cathodic electrochemical polarization has been demonstrated to be a valuable approach to boost the exsolution especially from titanate based structures, obtaining higher dispersions than that derived from thermal reduction 8 . In this work, we explored for the first time the behaviour of the double perovskite Sr 2 FeMo 0.6 Ni 0.4 O 6-δ (SFMN) under cathodic polarization and we investigated the impact of the structural evolution on the electrochemical performances of a multi-functional electrode for H 2 -SOFC and CO 2 -SOEC applications. 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Distribution of relaxation times (DRT) analyses was also used to obtain further insights on the impedance of the different cell mechanisms according to their characteristic frequency. The exsolved metal nanoparticles contributed to improve the conductivity and activity of the electrode, however, also the formation of RP phase seems have a significant role, especially in the electroreduction of CO 2 . Further studies are in progress to better understand the mechanisms of interaction between the phases formed during the exsolution process and their role on SOC electrodes activity. References 1 Hauch et al., Science 370, eaba6118 (2020). 2 M.B. Mogensen et al. Clean Energy, 3 (2019) 175–201 3 F. Salomone et.al Chem. Eng. Journal 377 (2019) , 120233 4.Irvine, J. T. S. Perovskite Oxide Anodes for SOFCs. In Perovskite Oxide for Solid Oxide Fuel Cells ; Ishihara, T., Ed.; Springer US: Boston, MA, 2009; pp 167–182. 5. W. Yin, et al. Energy Environ. Sci. 12 ( 2019 ) 442–462 6. Q. Islam, et al. 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引用次数: 0

摘要

固体氧化物电池(SOCs)是目前最有前途的能量转换技术之一,可以加速和促进基于可再生资源的能源转型1,2。事实上,这些设备允许开发有价值的低碳足迹的能量转换和存储链(X=电力,燃料)。在这方面是至关重要的创新,具有成本效益的材料和工艺的设计越来越多的通用和可逆的设备。在过去的十年中,简单钙钛矿(ABO 3)和双钙钛矿(a2 BB O 6)氧化物已被证明是金属陶瓷SOC电极的有价值的替代品,这得益于它们相对容易通过掺杂和溶出实现功能化以及它们的混合离子电子传导4-6。析出过程在很大程度上取决于金属和钙钛矿的类型以及诱导还原所采用的方法7。阴极电化学极化已被证明是一种有价值的方法,可以促进钛酸盐基结构的析出,获得比热还原得到的更高的分散度8。在这项工作中,我们首次探索了双钙钛矿Sr 2 FeMo 0.6 Ni 0.4 O 6-δ (SFMN)在阴极极化下的行为,并研究了结构演变对用于h2 -SOFC和CO 2 -SOEC的多功能电极电化学性能的影响。采用溶胶-凝胶法制备SFMN,并制备了负载式SFMN/ La 0.8 Sr 0.2 Ga 0.8 Mg 0.2 O 3-δ (LSGM)/La 0.6 Sr 0.4 Fe 0.8 Co 0.2 O 3-δ:Ce 0.9 Gd 0.1 O 2-δ (LSFCo:GDC)电池,在850℃下进行了热还原和电化学还原前后的测试。如前所述,SFMN的热还原导致金属纳米颗粒(Ni或Ni- fe合金)的析出和Ruddlesden-Popper相9 (RP)的原位形成。对测试电池的HRTEM, SEM和XRD表征表明,与热还原相比,钙钛矿在阴极极化下的结构转变加速。这使得我们能够深入了解整个转化过程在细胞电化学行为中的作用。采用EIS分析研究了SFNM的电化学性能。弛豫时间分布(DRT)分析也用于进一步了解不同细胞机制根据其特征频率的阻抗。溶解的金属纳米颗粒有助于提高电极的电导率和活性,然而,RP相的形成似乎也有重要的作用,特别是在CO 2的电还原中。为了更好地了解析出过程中形成的相之间的相互作用机制及其对SOC电极活性的影响,进一步的研究正在进行中。1 Hauch et al., Science 370, eaba6118(2020)。2 M.B. Mogensen等。清洁能源,3 (2019):175-201 3 F。Salomone等化学。Eng。[3]中国科学:自然科学版(2019),1233 - 1233。ervine, j.t.s。sofc的钙钛矿氧化物阳极。固体氧化物燃料电池用钙钛矿氧化物石原,T., Ed;斯普林格美国:波士顿,马萨诸塞州,2009;页167 - 182。5. 尹伟,等。能源环境。科学通报,12 (2019):442-462Q. Islam等人。[j] .能源科学与技术,2016,(2):1 - 6。7. O. Kwon等。期刊。能源学报,(2020),032001Jh,明,Jh。et al。《自然》,(2016)528-531。z;中国生物医学工程学报,2016,33 (2):669 - 669
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Study on Exsolution Process of Sr2FeMo0.6Ni0.4O6 via in Situ Cathodic Polarization
Solid oxide cells (SOCs) are nowadays one of the most promising energy conversion technologies, to accelerate and promote the ongoing energy transition 1,2 , based on the use of renewable resources. These devices in fact allow the development of valuable low carbon footprint power-to-X (X= power, fuels) chains of energy conversion and storage 3 . In this respect is crucial the design of innovative, cost-effective materials and processes for more and more versatile and reversible devices. In the last decade, simple perovskite (ABO 3 ) and double perovskite (A 2 BBʹO 6 ) oxide have been proved to be a valuable alternative to cermet SOC electrodes, thanks to their relative ease of functionalization via doping and exsolution and their mixed ionic-electron conduction 4-6 . Exsolution process is strongly dependent on the type of metal and perovskite and on methodology adopted to induce the reduction 7 . Cathodic electrochemical polarization has been demonstrated to be a valuable approach to boost the exsolution especially from titanate based structures, obtaining higher dispersions than that derived from thermal reduction 8 . In this work, we explored for the first time the behaviour of the double perovskite Sr 2 FeMo 0.6 Ni 0.4 O 6-δ (SFMN) under cathodic polarization and we investigated the impact of the structural evolution on the electrochemical performances of a multi-functional electrode for H 2 -SOFC and CO 2 -SOEC applications. SFMN was prepared by sol gel method and used to prepare supported SFMN/ La 0.8 Sr 0.2 Ga 0.8 Mg 0.2 O 3-δ (LSGM)/La 0.6 Sr 0.4 Fe 0.8 Co 0.2 O 3-δ :Ce 0.9 Gd 0.1 O 2-δ (LSFCo:GDC) cells that were tested either before and after thermal or electrochemical reduction at 850°C. As already reported the thermal reduction of SFMN leads to the exsolution of metal nanoparticles (of Ni or Ni-Fe alloys) and the in situ formation of Ruddlesden-Popper phase 9 (RP). HRTEM, SEM and XRD characterizations of tested cells allowed to observe an acceleration of the structural transformation of perovskite under cathodic polarization in comparison to what observed under thermal reduction. This allows to gain insights on the role of entire transformation on the electrochemical behaviours of cells. Electrochemical properties of SFNM were investigated by EIS analysis. Distribution of relaxation times (DRT) analyses was also used to obtain further insights on the impedance of the different cell mechanisms according to their characteristic frequency. The exsolved metal nanoparticles contributed to improve the conductivity and activity of the electrode, however, also the formation of RP phase seems have a significant role, especially in the electroreduction of CO 2 . Further studies are in progress to better understand the mechanisms of interaction between the phases formed during the exsolution process and their role on SOC electrodes activity. References 1 Hauch et al., Science 370, eaba6118 (2020). 2 M.B. Mogensen et al. Clean Energy, 3 (2019) 175–201 3 F. Salomone et.al Chem. Eng. Journal 377 (2019) , 120233 4.Irvine, J. T. S. Perovskite Oxide Anodes for SOFCs. In Perovskite Oxide for Solid Oxide Fuel Cells ; Ishihara, T., Ed.; Springer US: Boston, MA, 2009; pp 167–182. 5. W. Yin, et al. Energy Environ. Sci. 12 ( 2019 ) 442–462 6. Q. Islam, et al. J. Power Sources 492 ( 2021 ) , 229626. 7. O. Kwon et.al. J. Phys. Energy2, ( 2020) , 032001 8. Jh, Myung, Jh. et al. Nature 537, (2016) 528–531 9. Z.; Du et.al ACS Nano 10 , 2016 , 8660–8669
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