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Gelatin-derived sustainable carbon-based functional materials for energy conversion and storage with controllability of structure and component

机译:明胶衍生的可持续碳基功能材料用于能量转换和存储结构和组件可控

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摘要

Nonprecious carbon catalysts and electrodes are vital components in energy conversion and storage systems. Despite recent progress, controllable synthesis of carbon functional materials is still a great challenge. We report a novel strategy to prepare simultaneously Fe-N-C catalysts and Fe3O4/N-doped carbon hybrids based on the sol-gel chemistry of gelatin and iron with controllability of structure and component. The catalysts demonstrate higher catalytic activity and better durability for oxygen reduction than precious Pt/C catalysts. The active sites of FeN4/C (D1) and N-FeN2+2/C (D3) are identified by Mössbauer spectroscopy, and most of the Fe ions are converted into D1 or D3 species. The oxygen reduction reaction (ORR) activity correlates well with the surface area, porosity, and the content of active Fe-Nx /C (D1 + D3) species. As an anode material for lithium storage, Fe3O4/carbon hybrids exhibit superior rate capability and excellent cycling performance. The synthetic approach and the proposed mechanism open new avenues for the development of sustainable carbon-based functional materials.
机译:非贵金属催化剂和电极是能量转换和存储系统中的重要组成部分。尽管有最近的进展,但是碳功能材料的可控合成仍然是一个巨大的挑战。我们报告了一种基于明胶和铁的溶胶-凝胶化学同时具有结构和组分可控性的同时制备Fe-N-C催化剂和Fe3O4 / N掺杂的碳杂化物的新策略。与珍贵的Pt / C催化剂相比,该催化剂表现出更高的催化活性和更好的氧还原耐久性。 FeN4 / C(D1)和N-FeN2 + 2 / C(D3)的活性位点通过Mössbauer光谱法鉴定,大多数Fe离子被转化为D1或D3物种。氧还原反应(ORR)活性与表面积,孔隙率和活性Fe-Nx / C(D1 + D3)种类的含量密切相关。作为用于锂存储的阳极材料,Fe3O4 /碳杂化物表现出优异的速率能力和出色的循环性能。合成方法和拟议的机制为开发可持续的碳基功能材料开辟了新途径。

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