Wu Huali, Singh-Morgan Amrita, Qi Kun, Zeng Zhiyuan, Mougel Victor, Voiry Damien
Institut Européen des Membranes, IEM, UMR 5635, Université Montpellier, ENSCM, CNRS, Montpellier 34000, France.
Department of Chemistry and Applied Biosciences, ETH Zürich, Zürich 8093, Switzerland.
ACS Catal. 2023 Apr 6;13(8):5375-5396. doi: 10.1021/acscatal.3c00201. eCollection 2023 Apr 21.
Carbon and nitrogen fixation strategies are regarded as alternative routes to produce valuable chemicals used as energy carriers and fertilizers that are traditionally obtained from unsustainable and energy-intensive coal gasification (CO and CH), Fischer-Tropsch (CH), and Haber-Bosch (NH) processes. Recently, the electrocatalytic CO reduction reaction (CORR) and N reduction reaction (NRR) have received tremendous attention, with the merits of being both efficient strategies to store renewable electricity while providing alternative preparation routes to fossil-fuel-driven reactions. To date, the development of the CORR and NRR processes is primarily hindered by the competitive hydrogen evolution reaction (HER); however, the corresponding strategies for inhibiting this undesired side reaction are still quite limited. Considering such complex reactions involve three gas-liquid-solid phases and successive proton-coupled electron transfers, it appears meaningful to review the current strategies for improving product selectivity in light of their respective reaction mechanisms, kinetics, and thermodynamics. By examining the developments and understanding in catalyst design, electrolyte engineering, and three-phase interface modulation, we discuss three key strategies for improving product selectivity for the CORR and NRR: (i) targeting molecularly defined active sites, (ii) increasing the local reactant concentration at the active sites, and (iii) stabilizing and confining product intermediates.
碳固定和氮固定策略被视为生产用作能量载体和肥料的有价值化学品的替代途径,这些化学品传统上是通过不可持续且能源密集型的煤气化(CO和CH)、费托合成(CH)以及哈伯-博施(NH)工艺获得的。最近,电催化CO还原反应(CORR)和N还原反应(NRR)受到了极大关注,它们具有既能高效存储可再生电力,又能为化石燃料驱动的反应提供替代制备路线的优点。迄今为止,CORR和NRR工艺的发展主要受到竞争性析氢反应(HER)的阻碍;然而,抑制这种不期望的副反应的相应策略仍然相当有限。考虑到此类复杂反应涉及气-液-固三相以及连续的质子耦合电子转移,根据各自的反应机理、动力学和热力学来回顾当前提高产物选择性的策略似乎是有意义的。通过研究催化剂设计、电解质工程和三相界面调制方面的进展并加以理解,我们讨论了提高CORR和NRR产物选择性的三个关键策略:(i)靶向分子定义的活性位点;(ii)提高活性位点处的局部反应物浓度;(iii)稳定并限制产物中间体。