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Understanding the effects of material properties and operating conditions on component aging in polymer electrolyte water electrolyzers

机译:了解材料特性和操作条件对聚合物电解质水电解槽中部件老化的影响

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摘要

If polymer electrolyte water electrolysis (PEWE) is to penetrate the energy market in the context of power-to-x, challenges related to component durability need to be understood and addressed. In this study, PEWE component degradation mechanisms are induced by combining catalyst-coated membranes (CCMs) with specific cell materials and operating conditions. The effect of the cell compression on the catalyst layer performance is investigated using cell assemblies with porous transport layers (PTLs) having different material properties. Rigid PTL-surface features result in local variation in anode catalyst layer (CL) porosity, and increased CL proton transport resistance. The creep of the CCM leads to the formation of thin sections and an increase in the content of H-2 in the O-2 product gas, causing in turn higher fluoride release rate from the ionomer/membrane. In addition, PEWE cells are subjected to a start-stop protocol to promote catalyst degradation through the formation of active, but unstable iridium hydroxo species. An increasing trend of catalyst dissolution is observed in the case of CCM samples that were operated at higher potential.
机译:如果聚合物电解质水电解(PEWE)在power-to-x的背景下打入能源市场,则需要理解和解决与组件耐久性相关的挑战。在这项研究中,PEWE组分降解机理是通过将催化剂涂覆的膜(CCM)与特定的电池材料和操作条件结合在一起而引起的。使用具有不同材料性能的多孔传输层(PTL)的电池组件研究了电池压缩对催化剂层性能的影响。刚性的PTL表面特征会导致阳极催化剂层(CL)孔隙率局部变化,并增加CL质子传输阻力。 CCM的蠕变导致形成薄截面,并增加O-2产物气体中H-2的含量,进而导致离聚物/膜的氟化物释放速率更高。另外,对PEWE电池进行启动-停止方案以通过形成活性但不稳定的铱羟基物质来促进催化剂降解。在以较高电势操作的CCM样品中,观察到催化剂溶解的增加趋势。

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