{"title":"用于 PEM 水电解器的复合阳极:使用导电添加剂降低铱含量和材料成本","authors":"Kara J. Ferner, and , Shawn Litster*, ","doi":"10.1021/acsaem.4c0186610.1021/acsaem.4c01866","DOIUrl":null,"url":null,"abstract":"<p >To enable the greater installed capacity of proton exchange membrane water electrolysis (PEMWE) for clean hydrogen production, associated costs must be lowered while achieving high current density performance and durability. Scarce and expensive iridium (Ir) required for the oxygen evolution reaction (OER) is a large contributor to the overall cost, yet high loadings of Ir (1–2 mg<sub>Ir</sub> cm<sup>–2</sup>) are currently needed in commercial systems to maintain sufficient activity, conductivity, and durability. To meet the aggressive targets for low Ir loadings, we introduce a composite anode approach using a conductive additive that is less expensive than Ir to facilitate robust, high-performance operation with low Ir loading by retaining electrode thickness and in-plane electrical conductivity. In this demonstration, we use platinum (Pt) black as the conductive additive given its high electrical conductivity, acid stability, and current price one-fifth that of Ir. Using a high-activity commercial Ir oxide (IrO<i><sub>x</sub></i>) catalyst, we present a 95% Ir loading reduction and 80% cost reduction of the anode catalyst materials while maintaining equal current density performance at a cell voltage of 1.8 V. Furthermore, we show enhanced stability of a composite anode compared to an IrO<i><sub>x</sub></i> anode with loadings of 0.10 mg<sub>Ir</sub> cm<sup>–2</sup> via accelerated stress test (AST) and postmortem imaging. 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引用次数: 0
摘要
为了提高质子交换膜水电解法(PEMWE)用于清洁制氢的装机容量,必须在实现高电流密度性能和耐用性的同时降低相关成本。氧进化反应(OER)所需的铱(Ir)稀缺且昂贵,是造成总成本的主要原因,但目前在商业系统中需要较高的铱负载量(1-2 mgIr cm-2),以保持足够的活性、导电性和耐用性。为了达到低 Ir 负载的苛刻目标,我们引入了一种复合阳极方法,使用比 Ir 更便宜的导电添加剂,通过保持电极厚度和面内导电性,在低 Ir 负载的情况下实现稳健、高性能的运行。在这次演示中,我们使用铂(Pt)黑作为导电添加剂,因为它具有高导电性、酸稳定性,而且目前的价格只有 Ir 的五分之一。通过使用高活性的商用氧化铱(IrOx)催化剂,我们发现在电池电压为 1.8 V 时,铱的负载量减少了 95%,阳极催化剂材料的成本降低了 80%,同时保持了相同的电流密度性能。此外,通过加速应力测试 (AST) 和死后成像,我们还展示了复合阳极与负载量为 0.10 mgIr cm-2 的氧化铱阳极相比所具有的更高稳定性。通过这种方法,我们在降低Ir负载和材料成本方面取得了可喜的成果,解决了广泛采用PEMWE进行清洁制氢的重大障碍。
Composite Anode for PEM Water Electrolyzers: Lowering Iridium Loadings and Reducing Material Costs with a Conductive Additive
To enable the greater installed capacity of proton exchange membrane water electrolysis (PEMWE) for clean hydrogen production, associated costs must be lowered while achieving high current density performance and durability. Scarce and expensive iridium (Ir) required for the oxygen evolution reaction (OER) is a large contributor to the overall cost, yet high loadings of Ir (1–2 mgIr cm–2) are currently needed in commercial systems to maintain sufficient activity, conductivity, and durability. To meet the aggressive targets for low Ir loadings, we introduce a composite anode approach using a conductive additive that is less expensive than Ir to facilitate robust, high-performance operation with low Ir loading by retaining electrode thickness and in-plane electrical conductivity. In this demonstration, we use platinum (Pt) black as the conductive additive given its high electrical conductivity, acid stability, and current price one-fifth that of Ir. Using a high-activity commercial Ir oxide (IrOx) catalyst, we present a 95% Ir loading reduction and 80% cost reduction of the anode catalyst materials while maintaining equal current density performance at a cell voltage of 1.8 V. Furthermore, we show enhanced stability of a composite anode compared to an IrOx anode with loadings of 0.10 mgIr cm–2 via accelerated stress test (AST) and postmortem imaging. With this approach, we show promising results toward lowering Ir loadings and material costs, addressing a significant barrier to the widespread adoption of PEMWE for clean hydrogen production.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.