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Tea-leaf-residual derived electrocatalyst: Hierarchical pore structure and self nitrogen and fluorine co-doping for efficient oxygen reduction reaction

机译:茶叶残渣衍生的电催化剂:分层孔隙结构和自氮和氟共掺杂以有效进行氧还原反应

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The heteroatom-doped carbon materials as metal-free catalysts show great potential for oxygen reduction reaction (ORR) due to the high electrocatalytic activity, low cost, long-term stability, and environmental friendliness. Utilizing biomass as precursors has offered facile and extremely low-cost strategy to large-scale fabrication of highly efficient carbon materials with abundant pore structures and elements. In this work, tea residue was used as precursor to synthesize nitrogen (N) and fluorine (F) co-doped porous carbon materials via one-step annealing process without any activation or post-treatment. The morphology, pore structure, elemental composition of our sample as well as its electrocatalytic performance in ORR were studied. This biomass-based carbon materials has high specific surface area (855.6 m(2) g(-1)) and hierarchical pore structure, which can offer abundant active sites and meanwhile is favorable to ion diffusion of liquid electrolyte. Secondly, the heteroatoms (especially F) doping can induce charge redistribution thanks to the electronegativity difference, which can facilitate electron transfer in ORR. When compared to commercial Pt/C, our catalyst shows a higher limited current density and a high electron transfer number of about 3.8. Finally, the catalyst also demonstrates excellent methanol tolerance in the alkaline medium. Our work provides an economical and facile strategy to synthesize efficient electrocatalyst for ORR. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:由于具有高的电催化活性,低成本,长期稳定性和环境友好性,作为无金属催化剂的杂原子掺杂碳材料显示出巨大的氧还原反应(ORR)潜力。利用生物质作为前体为大规模制造具有丰富孔结构和元素的高效碳材料提供了简便且极低成本的策略。在这项工作中,茶渣被用作前驱体,通过一步退火工艺合成了氮(N)和氟(F)共掺杂的多孔碳材料,而没有进行任何活化或后处理。研究了样品的形貌,孔结构,元素组成及其在ORR中的电催化性能。这种基于生物质的碳材料具有高的比表面积(855.6 m(2)g(-1))和分层的孔结构,可以提供丰富的活性位,同时有利于液体电解质的离子扩散。其次,由于电负性差异,杂原子(尤其是F)掺杂会引起电荷重新分布,从而促进ORR中的电子转移。与市售Pt / C相比,我们的催化剂显示出更高的极限电流密度和约3.8的高电子转移数。最后,该催化剂还显示出在碱性介质中优异的甲醇耐受性。我们的工作提供了一种经济实用的策略来合成ORR的高效电催化剂。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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