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孔修饰和磷掺杂对用于碱性氧还原反应的磷酸活化Fe-N-C的影响

Pore Modification and Phosphorus Doping Effect on Phosphoric Acid-Activated Fe-N-C for Alkaline Oxygen Reduction Reaction.

作者信息

Kim Jong Gyeong, Han Sunghoon, Pak Chanho

机构信息

Graduate School of Energy Convergence, Institute of Integrated Technology, Gwangju Institute of Science and Technology, Gwangju 61005, Korea.

出版信息

Nanomaterials (Basel). 2021 Jun 8;11(6):1519. doi: 10.3390/nano11061519.

Abstract

The price and scarcity of platinum has driven up the demand for non-precious metal catalysts such as Fe-N-C. In this study, the effects of phosphoric acid (PA) activation and phosphorus doping were investigated using Fe-N-C catalysts prepared using SBA-15 as a sacrificial template. The physical and structural changes caused by the addition of PA were analyzed by nitrogen adsorption/desorption and X-ray diffraction. Analysis of the electronic states of Fe, N, and P were conducted by X-ray photoelectron spectroscopy. The amount and size of micropores varied depending on the PA content, with changes in pore structure observed using 0.066 g of PA. The electronic states of Fe and N did not change significantly after treatment with PA, and P was mainly found in states bonded to oxygen or carbon. When 0.135 g of PA was introduced per 1 g of silica, a catalytic activity which was increased slightly by 10 mV at -3 mA/cm was observed. A change in Fe-N-C stability was also observed through the introduction of PA.

摘要

铂的价格和稀缺性推动了对诸如Fe-N-C等非贵金属催化剂的需求。在本研究中,使用以SBA-15作为牺牲模板制备的Fe-N-C催化剂,研究了磷酸(PA)活化和磷掺杂的效果。通过氮气吸附/脱附和X射线衍射分析了添加PA引起的物理和结构变化。通过X射线光电子能谱对Fe、N和P的电子态进行了分析。微孔的数量和尺寸随PA含量而变化,使用0.066 g PA时观察到孔结构的变化。用PA处理后,Fe和N的电子态没有明显变化,P主要以与氧或碳结合的状态存在。当每1 g二氧化硅引入0.135 g PA时,在-3 mA/cm下观察到催化活性略有增加,增加了10 mV。通过引入PA还观察到Fe-N-C稳定性的变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fc5/8229517/57974a00b81c/nanomaterials-11-01519-g001a.jpg

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