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Platinum-Alloy Cathode Catalyst Degradation in Proton Exchange Membrane Fuel Cells: Nanometer-Scale Compositional and Morphological Changes

机译:质子交换膜燃料电池中铂 - 合金阴极催化剂降解:纳米级成分和形态变化

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摘要

Electrochemical measurements showed an ≈75% Pt surface area loss and an ≈40% specific activity loss for a membrane electrode assembly (MEA) cathode with acid-treated “Pt[subscript 3]Co ” catalyst particles in a H[subscript 2]/N[subscript 2] proton exchange membrane fuel cell after 24h voltage cycling between 0.65 and 1.05V vs reversible hydrogen electrode. Transmission electron microscopy, scanning transmission electron microscopy, associated X-ray energy dispersive spectroscopy, and high angle annular dark-field techniques were used to probe the microstructural changes of the MEA cathode and the compositional changes along the MEA cathode thickness and within individual Pt[subscript x]Co nanoparticles before and after voltage cycling. Further Co dissolution from acid-treated Pt[subscript x]Co particles that leads to an increased thickness of a Pt-enriched surface layer and the development of core/shell Pt[subscript x]Co particles was largely responsible for the reduction in the specific activity of Pt[subscript x]Co nanoparticle after potential cycling. The Pt weight loss associated with the formation of Pt crystallites near the cathode/membrane interface largely contributed to the measured electrochemical surface area loss, while particle growth of the Pt[subscript x]Co particles via Ostwald ripening played a lesser role.
机译:电化学测量显示含有酸处理的“Pt [下标3] Co”催化剂颗粒的膜电极组件(MEA)阴极的含有酸处理的“Pt [下标3] Co”催化剂颗粒的≈75%Pt表面积损失和≈40%的特定活性损失。 N [下标2]质子交换膜燃料电池在24h电压循环后0.65和1.05V Vs可逆氢电极。透射电子显微镜,扫描透射电子显微镜,相关的X射线能量分散光谱和高角度环形暗场技术用于探测MEA阴极的微观结构变化和沿着MEA阴极厚度和单独的PT内的组成变化[下标X] CO纳米颗粒前后电压循环。来自酸处理的Pt [下标X] Co颗粒的进一步溶解,其导致Pt富集的表面层的厚度增加,并且核/壳Pt [下标X] Co颗粒的显影很大程度上负责所述特定的减少潜在循环后Pt [下标X] Co纳米粒子的活性。与在阴极/膜界面附近形成Pt微晶相关的Pt重量损失在很大程度上导致了测量的电化学表面积损失,而Pt [下标x] Co颗粒的颗粒生长通过Ostwald成熟的作用较小。

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