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理解用于高温应用的纳米级镍钆掺杂二氧化铈电极中的粗化和降解。

Understanding the Coarsening and Degradation in a Nanoscale Nickel Gadolinia-Doped-Ceria Electrode for High-Temperature Applications.

作者信息

Chen Jingyi, Ouyang Mengzheng, Boldrin Paul, Atkinson Alan, Brandon Nigel P

机构信息

Department of Materials, Imperial College, London SW7 2AZ, U.K.

Dyson School of Design Engineering, Imperial College, London SW7 2AZ, U.K.

出版信息

ACS Appl Mater Interfaces. 2020 Oct 21;12(42):47564-47573. doi: 10.1021/acsami.0c13784. Epub 2020 Oct 12.

DOI:10.1021/acsami.0c13784
PMID:33044810
Abstract

Nanostructure engineering is an effective approach to enhance the electrochemical performance of energy devices. While the high surface area of nanoparticles greatly enlarges the density of reaction sites, it often also leads to relatively rapid degradation as the particles tend to coarsen to reduce their high surface energy. Therefore, a nickel/gadolinia-doped-ceria (CGO) cermet electrode is studied, with a novel porous nanostructure consisting of nanoscale Ni (100 nm) and CGO (50 nm) crystallites, cosintered from nanocomposite precursor agglomerate particles. This electrode combines both high performance and excellent durability, with a total area-specific resistance (ASR) of 0.11 Ω cm at 800 °C and a stable ASR with up to 170 h ageing in humidified 5% H-N. Post-test analysis by 3D tomography shows that nickel coarsens and is responsible for the initial increase in ASR. However, the subsequent electrochemical performance is stable because reaction at the double phase boundaries (DPBs) on the surfaces of nanoscale CGO becomes dominant and is resistant to ageing. At this stage, the coarsened Ni network is also stabilized by the surrounding nanostructure. The dominant role of the DPB reaction is supported quantitatively using a continuum model with geometrical parameters obtained from 3D tomography.

摘要

纳米结构工程是提高能量装置电化学性能的有效方法。虽然纳米颗粒的高表面积极大地增加了反应位点的密度,但由于颗粒倾向于粗化以降低其高表面能,这通常也会导致相对快速的降解。因此,研究了一种镍/钆掺杂二氧化铈(CGO)金属陶瓷电极,它具有由纳米级镍(100纳米)和CGO(50纳米)微晶组成的新型多孔纳米结构,由纳米复合前驱体团聚颗粒共烧结而成。该电极兼具高性能和出色的耐久性,在800℃时的总面积比电阻(ASR)为0.11Ω·cm,在加湿的5%H-N中老化长达170小时时ASR稳定。通过三维断层扫描进行的测试后分析表明,镍粗化是ASR初始增加的原因。然而,随后的电化学性能是稳定的,因为纳米级CGO表面双相边界(DPB)处的反应占主导地位且抗老化。在此阶段,粗化的镍网络也被周围的纳米结构稳定。使用从三维断层扫描获得几何参数的连续模型定量支持了DPB反应的主导作用。

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