Valorization of Naturally Abundant Low-Value Peat into Highly Active Non-Platinum Group Metal Oxygen Reduction Catalysts

Patrick Teppor, Rutha Jäger, Jaak Nerut, Miriam Koppel, Jaan Aruväli, Olga Volobujeva, Enn Lust
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Abstract

As society continues to adopt an increasingly eco-friendly stance, the efficient usage of natural resources needs to be maximised. For instance, energy obtained from biomass covers roughly a tenth of the global demand. This biomass can instead be used as a carbon source to produce value-added materials such as tnon-platinum group metal (NPGM) oxygen reduction catalysts, which are desperately sought after as global demand for fuel cells continues to rise [1,2]. For example, peat is an extremely abundant biomass material in Estonia covering roughly 20% of the country [3]. Herein, the viability of using peat-based catalysts as oxygen reduction catalysts in alkaline media was investigated. The peat sourced from a local peatland was processed and modified with inexpensive iron and nitrogen precursors through the common double-pyrolysis and acid washing synthesis procedure into peat-based NPGM catalysts. Additionally, zinc chloride was used as a pore forming agent. The influence of several principal synthesis parameters, e.g. precursor compound type and amount, on the physical and electrochemical properties of these materials was investigated using various characterization methods. The NPGM catalysts obtained from naturally abundant peat were highly microporous systems due to the inclusion of zinc chloride in the synthesis mixture. High onset (~0.93 V vs RHE) and half-wave potential (~0.83 V vs RHE) values were obtained for most of the materials in activity screening experiments conducted with a rotating disc electrode setup using 0.1 M KOH. However, using an excessive amount of the nitrogen precursor in the synthesis proved to be detrimental to the obtained activity. The high activity of the obtained peat-derived catalysts was further investigated in a rotating ring disc electrode setup where the influence of the studied synthesis parameters on the oxygen reduction reaction selectivity was more evident. Acknowledgments This work was supported by the EU through the European Regional Development Fund under projects TK141 “Advanced materials and high-technology devices for energy recuperation systems” (2014-2020.4.01.15-0011), NAMUR “Nanomaterials - research and applications” (3.2.0304.12-0397), NAMUR+ core facility funded by the Estonian Research Council (TT 13), PRG676 “Development of express analysis methods for micro-mesoporous materials for Estonian peat derived carbon supercapacitors” (01.01.2020–31.12.2024) and PUT1581 (1.01.2017–31.12.2020). References F. Jaouen, D. Jones, N. Coutard, V. Artero, P. Strasser, A. Kucernak, Johns. Matthey Technol Rev. 2018, 62, 231. E4tech, 2022, The Fuel Cell Industry Review 2021 . M. Orru, H. Orru, Est. J. Earth Sci. 2008, 57, 87.
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天然丰富的低价值泥炭转化为高活性非铂族金属氧还原催化剂的研究
随着社会继续采取越来越环保的立场,需要最大限度地有效利用自然资源。例如,从生物质能中获得的能源约占全球需求的十分之一。这种生物质可以作为碳源来生产增值材料,如非铂族金属(NPGM)氧还原催化剂,随着全球对燃料电池的需求持续上升,这种材料受到了迫切的追捧[1,2]。例如,泥炭是爱沙尼亚极其丰富的生物质材料,约占该国面积的20%[3]。本文研究了在碱性介质中使用泥炭基催化剂作为氧还原催化剂的可行性。从当地泥炭地获取泥炭,通过常见的双热解和酸洗合成工艺,用廉价的铁和氮前体对其进行处理和改性,制备出泥炭基NPGM催化剂。另外,氯化锌作为成孔剂。采用不同的表征方法研究了前驱体化合物类型和用量等主要合成参数对材料物理和电化学性能的影响。从天然丰富的泥炭中获得的NPGM催化剂由于在合成混合物中包含氯化锌而具有高度微孔体系。在0.1 M KOH的旋转圆盘电极装置上进行的活性筛选实验中,大多数材料获得了高起始电位(~0.93 V vs RHE)和半波电位(~0.83 V vs RHE)值。然而,在合成中使用过量的氮前体被证明对获得的活性是有害的。在旋转环盘式电极装置上进一步研究了所制备的泥炭系催化剂的高活性,其中合成参数对氧还原反应选择性的影响更为明显。本工作由欧盟通过欧洲区域发展基金项目TK141“能源回收系统的先进材料和高科技设备”(2014-2020.4.01.15-0011),NAMUR“纳米材料-研究和应用”(3.2.0304.12-0397),NAMUR+核心设施由爱沙尼亚研究理事会(TT 13)资助。PRG676“爱沙尼亚泥炭衍生碳超级电容器微介孔材料快速分析方法的发展”(01.01.2020-31.12.2024)和PUT1581(1.01.2017-31.12.2020)。参考文献F. Jaouen, D. Jones, N. Coutard, V. Artero, P. Strasser, A. Kucernak, Johns。自动化学报,2018,62,231。E4tech, 2022, The Fuel Cell Industry Review 2021。张建军,张建军,张建军,等。地球科学进展,2008,32(1):1 - 4。
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