Fischer Robert, Dessiex Matthieu A, Marone Federica, Büchi Felix N
Electrochemistry Laboratory, Paul Scherrer Institut, 5232 Villigen PSI, Switzerland.
Laboratory of Renewable Energy Science and Engineering, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.
ACS Appl Energy Mater. 2024 Apr 19;7(9):3590-3601. doi: 10.1021/acsaem.3c02882. eCollection 2024 May 13.
Forward-bias bipolar membrane (BPM) CO coelectrolysis (CO2ELY) aims at overcoming the issues of salt precipitation and CO crossover in anion exchange membrane CO2ELY. Increasing the stability of BPM-CO2ELY is crucial for widespread application of the technique. In this study, we employ time-resolved X-ray tomographic microscopy to elucidate the structural dynamics that occur within the electrochemical cell during operation under various conditions. Using advanced image processing methods, including custom 4D machine learning segmentation, we can visualize and quantify damages in the membrane and anode catalyst layer (CL). We compare our results to a CO transport model and hypothesize gaseous CO as the cause of the observed damages. At any operation condition, CO is formed at the junction in the center of the BPM by recombination of carbonate ions. CO migrates to the anode by diffusion and goes into the gas phase at the interface of the membrane and anode CL. After sufficient CO accumulation and pressure buildup after only tens of minutes, small irreversible holes break into the CL distributed over the entire active area. Additionally, at higher current densities, the CO accumulation leads to membrane delamination at the BPM junction. Despite the clear degradation processes, we do not observe an obvious direct effect on the electrochemical performance. The poor stability of BPM-CO2ELY remains an open question.
正向偏置双极膜(BPM)CO共电解(CO2ELY)旨在克服阴离子交换膜CO2ELY中的盐沉淀和CO渗透问题。提高BPM-CO2ELY的稳定性对于该技术的广泛应用至关重要。在本研究中,我们采用时间分辨X射线断层扫描显微镜来阐明在各种条件下运行期间电化学电池内发生的结构动力学。使用先进的图像处理方法,包括定制的4D机器学习分割,我们可以可视化和量化膜和阳极催化剂层(CL)中的损伤。我们将结果与CO传输模型进行比较,并假设气态CO是观察到的损伤的原因。在任何操作条件下,CO在BPM中心的交界处通过碳酸根离子的重组形成。CO通过扩散迁移到阳极,并在膜和阳极CL的界面处进入气相。仅在几十分钟后,在足够的CO积累和压力增加后,小的不可逆孔在分布于整个活性区域的CL中形成。此外,在较高电流密度下,CO积累导致BPM交界处的膜分层。尽管有明显的降解过程,但我们没有观察到对电化学性能有明显的直接影响。BPM-CO2ELY的稳定性差仍然是一个悬而未决的问题。