材料科学
形态学(生物学)
催化作用
化学工程
碳纤维
表面结构
纳米技术
曲面(拓扑)
复合材料
结晶学
有机化学
几何学
复合数
生物
数学
工程类
遗传学
化学
作者
Robin Girod,Vasiliki Tileli
标识
DOI:10.1002/aenm.202500400
摘要
Abstract In proton exchange membrane fuel cells, the interior porosity of the standard high surface area carbon (HSC) supports anchors and shields catalysts, offering benefits in performance and durability. Yet, these carbons also add mass transport resistance. This delicate tradeoff relies on their interior diffusion pathways, which are difficult to fully characterize and remain poorly understood. Here, the multiscale morphology of HSCs is reported using full‐range electron tomography, resolving features down to single carbon planes. It is found that the supports typically feature a core‐shell morphology with large central pores and compact shell in which pores are slit‐shaped and sub‐nm in size, while entry points are 7–8 Å in diameter and are rarely in close proximity to Pt catalysts. This remarkably resolved structural landscape reveals that O 2 diffusion pathways in HSCs are narrower and longer than previously assumed, indicating the critical value of the carbon support redesign for optimizing cell performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI