Wenhao Ren, Huanlei Zhang, Miyeon Chang, Nanjun Chen, Wenchao Ma, Jun Gu, Meng Lin, Xile Hu
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引用次数: 0
Abstract
Zero-gap membrane electrode assembly (MEA) CO electrolyzer stands as a promising technology for circular carbon economy. However, current CO electrolyzers are energetically inefficient when operating at ampere-level current densities. Here, by analyzing the performance discrepancies between MEA and flow cells, we identify the depletion of K+ and water at the cathode as the main contributor to the low performance of MEA CO electrolyzers. This is attributed to the unique cathodic interface in catholyte-free MEA, where there is no aqueous electrolyte to maintain the three-phase interface. Through the development of needle-array catalysts with intensified electric fields (EFs) at their tips, we are able to concentrate the limited K+ cations onto the tips of the cathode, while simultaneously facilitating water uptake via electro-osmosis. We construct an MEA CO electrolyzer that achieves a large current density of 2,500 mA cm−2 at a voltage of only 2.7 V.
零间隙膜电极组件(MEA)一氧化碳电解槽是一种很有前途的循环碳经济技术。然而,目前的二氧化碳电解槽在安培级电流密度下运行时能量效率较低。在这里,通过分析 MEA 和流动电池之间的性能差异,我们发现阴极的 K+ 和水耗尽是导致 MEA CO 电解槽性能低下的主要原因。这归因于无阴极电解质 MEA 中独特的阴极界面,即没有水电解质来维持三相界面。通过开发针状阵列催化剂,并在其顶端加强电场 (EF),我们能够将有限的 K+ 阳离子集中到阴极顶端,同时通过电渗透促进水的吸收。我们构建的 MEA CO 电解槽在电压仅为 2.7 V 的情况下可达到 2,500 mA cm-2 的大电流密度。
期刊介绍:
Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.