Optimization of a Perovskite Oxide-Based Cathode Catalyst Layer on Performance of Direct Ammonia Fuel Cells

被引:6
作者
Jeerh, Georgina [1 ]
Zou, Peimiao [1 ]
Zhang, Mengfei [1 ]
Tao, Shanwen [1 ,2 ]
机构
[1] Univ Warwick, Sch Engn, Coventry CV4 7AL, Warwick, England
[2] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
基金
英国工程与自然科学研究理事会; “创新英国”项目;
关键词
direct ammonia fuel cell (DAFC); perovskite; cathode; catalyst layer; optimization; OXYGEN REDUCTION REACTION; ANION-EXCHANGE MEMBRANES; IONOMER CONTENT; RECENT PROGRESS; NAFION CONTENT; HYDROXIDE; TRANSPORT; CARBON; INK; ELECTROCATALYSTS;
D O I
10.1021/acsami.2c17253
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To maximize fuel cell performance, transport pathways for electrons, ions, and reactants should be connected well. This demands a well-constructed microstructure in the catalyst layer (CL). Herein we design and optimize a cathode CL for a direct ammonia fuel cell (DAFC) using a perovskite oxide as the catalyst to reduce reliance on platinum group metals (PGMs). The effects of tailoring carbon, ionomer, and polytetrafluoroethylene (PTFE) content in cathode CLs (CCLs) were explored, and several DAFCs were tested. Using the same catalyst and operating conditions, the lowest maximum current density and peak power density obtained were 85.3 mA cm-2 and 5.92 mW cm-2, respectively, which substantially increased to 317 mA cm-2 and 30.1 mW cm-2 through proper carbon, ionomer, and PTFE optimization, illustrating the importance of an effective three-phase interface. The findings reveal that despite employment of an active catalyst for oxygen reduction at the cathode site, the true performance of the catalyst cannot be reflected unless it is supported by proper design of the CCL. The study also reveals that by optimizing the CCL, similar performances to those of Pt/C-based CCLs in literature can be obtained at a cost reduction.
引用
收藏
页码:1029 / 1041
页数:13
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