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Influence of platinum group metal-free catalyst synthesis on microbial fuel cell performance

机译:不含铂族金属的催化剂合成对微生物燃料电池性能的影响

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摘要

Platinum group metal-free (PGM-free) ORR catalysts from the Fe-N-C family were synthesized using sacrificial support method (SSM) technique. Six experimental steps were used during the synthesis: 1) mixing the precursor, the metal salt, and the silica template; 2) first pyrolysis in hydrogen rich atmosphere; 3) ball milling; 4) etching the silica template using harsh acids environment; 5) the second pyrolysis in ammonia rich atmosphere; 6) final ball milling. Three independent batches were fabricated following the same procedure. The effect of each synthetic parameters on the surface chemistry and the electrocatalytic performance in neutral media was studied. Rotating ring disk electrode (RRDE) experiment showed an increase in half wave potential and limiting current after the pyrolysis steps. The additional improvement was observed after etching and performing the second pyrolysis. A similar trend was seen in microbial fuel cells (MFCs), in which the power output increased from 167 ± 2 μW cm−2 to 214 ± 5 μW cm−2. X-ray Photoelectron Spectroscopy (XPS) was used to evaluate surface chemistry of catalysts obtained after each synthetic step. The changes in chemical composition were directly correlated with the improvements in performance. We report outstanding reproducibility in both composition and performance among the three different batches.
机译:采用牺牲支撑法(SSM)合成了Fe-N-C族的无铂族金属(无PGM)ORR催化剂。在合成过程中使用了六个实验步骤:1)混合前体,金属盐和二氧化硅模板; 2)首先在富氢气氛中热解; 3)球磨; 4)在强酸环境下蚀刻二氧化硅模板; 5)在富氨气氛下进行第二次热解; 6)最后的球磨。按照相同的程序制造三个独立的批次。研究了各个合成参数对中性介质中表面化学和电催化性能的影响。旋转环盘电极(RRDE)实验表明,热解步骤后,半波电势和极限电流增加。在蚀刻并进行第二次热解后,观察到另外的改善。在微生物燃料电池(MFCs)中也看到了类似的趋势,其中功率输出从167±2μWcm -2 增加到214±5μWcm -2 。 X射线光电子能谱(XPS)用于评估每个合成步骤后获得的催化剂的表面化学性质。化学成分的变化与性能的提高直接相关。我们报告了三个不同批次在成分和性能方面均具有出色的可重复性。

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