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Synthesis, characterization, and durability study of Pt-Co hollow nanoparticles deposited on carbon xerogel electrocatalysts for Proton Exchange Membrane Fuel Cells (PEMFC)

机译:质子交换膜燃料电池用碳干凝胶电催化剂上沉积的Pt-Co空心纳米粒子的合成,表征和耐久性研究

摘要

Proton exchange membrane fuel cell (PEMFC) catalysts are generally made of carbon black (CB)supported platinum-based nanoparticles. However, the properties of CBs, as described by RodríguezReinoso [1], are not optimal for electrocatalysis. A possible solution to the drawbacks of CBs is the use of synthetic nanostructured materials with a controllable and reproducible texture and with a pure, known and constant chemical composition; carbon xerogels (CX) exhibit such properties [2].Recently, various highly dispersed CX-supported Pt nanoparticles catalysts (Pt/CX) have been synthesized via several methods, such as the strong electrostatic adsorption (SEA) [3] or the charge-enhanced dry impregnation (CEDI) [4].However, the decrease of the Pt mass contained in the PEMFC electrodes, in particular at the cathode where the oxygen reduction reaction (ORR) is processed, remains a major challenge. Improving the ORR mass activity is currently best achieved by alloying Pt with 3d-transition metal atoms such as cobalt (Co). These alloys perform better than the ORR because the substitution of some Pt atoms by 3d-metal atoms with smaller radius leads to a modified Pt electronic structure [5]. The synthesis and durability of Pt-Co hollow particles/CX (Fig. 1) is currently being studied in our groups. The results indicate that the specific and mass activity of the bimetallic hollow particles dispersed on CX is ca. 10 times higher than that of pure Pt/CB. The first durability results show good stability of the hollow particles structure. Performances and accelerated stress tests (ASTs) in PEMFCs were finally performed.
机译:质子交换膜燃料电池(PEMFC)催化剂通常由炭黑(CB)负载的铂基纳米颗粒制成。但是,如RodríguezReinoso[1]所述,CB的性质并非电催化的最佳选择。解决CB缺点的一种可能的解决方法是使用具有可控和可复制的质地,具有纯净,已知和恒定化学成分的合成纳米结构材料;碳干凝胶(CX)表现出这种特性[2]。最近,各种高度分散的CX负载的Pt纳米颗粒催化剂(Pt / CX)已通过多种方法合成,例如强静电吸附(SEA)[3]或电荷增强干浸渍(CEDI)[4]。但是,Pt的降低PEMFC电极中,尤其是在进行氧还原反应(ORR)的阴极处所包含的质量仍然是主要挑战。目前,通过将Pt与3d过渡金属原子(例如钴(Co))合金化,可以最佳地提高ORR质量活性。这些合金的性能优于ORR,因为用半径较小的3d金属原子取代了一些Pt原子会导致修饰的Pt电子结构[5]。目前正在我们的小组中研究Pt-Co空心颗粒/ CX的合成和耐久性(图1)。结果表明,分散在CX上的双金属空心颗粒的比活和质量活度约为。比纯Pt / CB高10倍。第一耐久性结果显示出中空颗粒结构的良好稳定性。最终在PEMFC中执行了性能和加速应力测试(AST)。

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