Cao Changsheng, Ma Dong-Dong, Jia Jingchun, Xu Qiang, Wu Xin-Tao, Zhu Qi-Long
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences (CAS), Fuzhou, 350002, China.
University of Chinese Academy of Sciences, Beijing, 100049, China.
Adv Mater. 2021 Jun;33(25):e2008631. doi: 10.1002/adma.202008631. Epub 2021 May 14.
Electrosynthesis of formic acid/formate is a promising alternative protocol to industrial processes. Herein, a pioneering pair-electrosynthesis tactic is reported for exclusively producing formate via coupling selectively electrocatalytic methanol oxidation reaction (MOR) and CO reduction reaction (CO RR), in which the electrode derived from Ni-based metal-organic framework (Ni-MOF) nanosheet arrays (Ni-NF-Af), as well as the Bi-MOF-derived ultrathin bismuthenes (Bi-enes), both obtained through an in situ electrochemical conversion process, are used as efficient anodic and cathodic electrocatalysts, respectively, achieving concurrent yielding of the same high-value product at both electrodes with greatly reduced energy input. The as-prepared Ni-NF-Af only needs quite low potentials to reach large current densities (e.g., 100 mA cm @1.345 V) with ≈100% selectivity for anodic methanol-to-formate conversion. Meanwhile, for CO RR in the cathode, the as-prepared Bi-enes can simultaneously exhibit near-unity selectivity, large current densities, and good stability in a wide potential window toward formate production. Consequently, the coupled MOR//CO RR system based on the distinctive MOF-derived catalysts displays excellent performance for pair-electrosynthesis of formate, delivering high current densities and nearly 100% selectivity for formate production in both the anode and the cathode. This work provides a novel way to design advanced MOF-derived electrocatalysts and innovative electrolytic systems for electrochemical production of value-added feedstocks.
甲酸/甲酸盐的电合成是一种有前景的工业生产替代方案。在此,报道了一种开创性的双电极电合成策略,通过将选择性电催化甲醇氧化反应(MOR)和CO还原反应(CO RR)耦合来专门生产甲酸盐,其中由镍基金属有机框架(Ni-MOF)纳米片阵列(Ni-NF-Af)衍生的电极以及通过原位电化学转化过程获得的Bi-MOF衍生的超薄铋烯(Bi-enes)分别用作高效的阳极和阴极电催化剂,在两个电极上同时产生相同的高价值产物,同时大幅降低了能量输入。所制备的Ni-NF-Af仅需相当低的电位就能达到大电流密度(例如,在1.345 V时为100 mA cm@),阳极甲醇到甲酸盐转化的选择性约为100%。同时,对于阴极中的CO RR,所制备的Bi-enes在宽电位窗口内对甲酸盐生产能同时表现出接近100%的选择性、大电流密度和良好的稳定性。因此,基于独特的MOF衍生催化剂的耦合MOR//CO RR系统在甲酸盐的双电极电合成中表现出优异的性能,在阳极和阴极都能提供高电流密度和近100%的甲酸盐生产选择性。这项工作为设计先进的MOF衍生电催化剂和创新的电解系统以电化学生产增值原料提供了一种新方法。