Morphology Evolution and Adsorption Behavior of Ionomers from Solution to Pt/C Substrates

被引:15
作者
Guo, Yuting [1 ]
Mabuchi, Takuya [1 ,2 ]
Li, Gaoyang [1 ]
Tokumasu, Takashi [1 ]
机构
[1] Tohoku Univ, Inst Fluid Sci, Sendai, Miyagi 9808577, Japan
[2] Tohoku Univ, Frontier Res Inst Interdisciplinary Sci, Sendai, Miyagi 9808577, Japan
关键词
MOLECULAR-DYNAMICS; CATALYST LAYER; SURFACTANT ADSORPTION; NAFION LONOMER; HEAT-TRANSFER; FUEL-CELLS; POLYMER; TRANSPORT; FILMS; SIMULATIONS;
D O I
10.1021/acs.macromol.2c00533
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Coarse-grained molecular dynamics simulations were performed to understand the morphological evolution and adsorption mechanism of Nafion ionomers from the aqueous solutions to the Pt/C substrate surface under various solution compositions and substrate properties. We found that the ionomer coverage did not increase with the increasing ionomer-to-carbon ratio but was related to the size and concentration of the ionomer aggregates, following the Langmuir adsorption model that shows a wettability switching behavior due to their changed morphology from solution to the surface. Ionomer aggregates in the solution tended to unfold and spread on the carbon substrate rather than Pt particles, although the cylindrical ionomer aggregates were easily attracted by Pt particles initially due to their hydrophilic ionic shells. The smaller Pt particles had a greater effect on ionomer adsorption. With the increasing number of Pt particles, ionomer coverage increased first and then decreased, depending on whether there was enough carbon surface to anchor the ionomer backbone. A balanced Pt/C ratio and the appropriate distribution of the Pt particles were required for tuning the ionomer coverage and distribution toward the design of the catalyst ink structure to improve the power performance.
引用
收藏
页码:4245 / 4255
页数:11
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