Liu Huiyuan, Zhao Jian, Li Xianguo
Department of Mechanical and Mechatronics Engineering, University of Waterloo, 200 University Avenue West, Waterloo, ON N2L 3G1 Canada.
Electrochem Energ Rev. 2022;5(4):13. doi: 10.1007/s41918-022-00173-3. Epub 2022 Sep 24.
Proton exchange membrane fuel cells are playing an increasing role in postpandemic economic recovery and climate action plans. However, their performance, cost, and durability are significantly related to Pt-based electrocatalysts, hampering their large-scale commercial application. Hence, considerable efforts have been devoted to improving the activity and durability of Pt-based electrocatalysts by controlled synthesis in recent years as an effective method for decreasing Pt use, and consequently, the cost. Therefore, this review article focuses on the synthesis processes of carbon-supported Pt-based electrocatalysts, which significantly affect the nanoparticle size, shape, and dispersion on supports and thus the activity and durability of the prepared electrocatalysts. The reviewed processes include (i) the functionalization of a commercial carbon support for enhanced catalyst-support interaction and additional catalytic effects, (ii) the methods for loading Pt-based electrocatalysts onto a carbon support that impact the manufacturing costs of electrocatalysts, (iii) the preparation of spherical and nonspherical Pt-based electrocatalysts (polyhedrons, nanocages, nanoframes, one- and two-dimensional nanostructures), and (iv) the postsynthesis treatments of supported electrocatalysts. The influences of the supports, key experimental parameters, and postsynthesis treatments on Pt-based electrocatalysts are scrutinized in detail. Future research directions are outlined, including (i) the full exploitation of the potential functionalization of commercial carbon supports, (ii) scaled-up one-pot synthesis of carbon-supported Pt-based electrocatalysts, and (iii) simplification of postsynthesis treatments. One-pot synthesis in aqueous instead of organic reaction systems and the minimal use of organic ligands are preferred to simplify the synthesis and postsynthesis treatment processes and to promote the mass production of commercial carbon-supported Pt-based electrocatalysts.
This review focuses on the synthesis process of Pt-based electrocatalysts/C to develop aqueous one-pot synthesis at large-scale production for PEMFC stack application.
质子交换膜燃料电池在疫情后经济复苏和气候行动计划中发挥着越来越重要的作用。然而,其性能、成本和耐久性与铂基电催化剂密切相关,这阻碍了它们的大规模商业应用。因此,近年来人们致力于通过可控合成来提高铂基电催化剂的活性和耐久性,作为减少铂用量从而降低成本的有效方法。因此,本文综述聚焦于碳载铂基电催化剂的合成过程,这显著影响纳米颗粒的尺寸、形状及其在载体上的分散情况,进而影响所制备电催化剂的活性和耐久性。所综述的过程包括:(i)对商业碳载体进行功能化以增强催化剂 - 载体相互作用和额外的催化效果;(ii)将铂基电催化剂负载到碳载体上的方法,这会影响电催化剂的制造成本;(iii)球形和非球形铂基电催化剂(多面体、纳米笼、纳米框架、一维和二维纳米结构)的制备;以及(iv)负载型电催化剂的合成后处理。详细审视了载体、关键实验参数和合成后处理对铂基电催化剂的影响。概述了未来的研究方向,包括:(i)充分挖掘商业碳载体潜在的功能化;(ii)扩大碳载铂基电催化剂的一锅法合成规模;以及(iii)简化合成后处理。优选在水性而非有机反应体系中进行一锅法合成,并尽量减少有机配体的使用,以简化合成和合成后处理过程,促进商业碳载铂基电催化剂的大规模生产。
本综述聚焦于铂基电催化剂/C的合成过程,以开发用于质子交换膜燃料电池堆应用的大规模水性一锅法合成。