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仿生制备 CeO 封装的氮自掺杂生物炭用于高效氧还原

Bionic Preparation of CeO-Encapsulated Nitrogen Self-Doped Biochars for Highly Efficient Oxygen Reduction.

机构信息

School of Resource and Environmental Science, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy , Wuhan University , Wuhan 430079 , China.

State Key Laboratory of Environmental Criteria and Risk Assessment , Chinese Research Academy of Environmental Sciences , Beijing 100012 , China.

出版信息

ACS Appl Mater Interfaces. 2020 Jan 22;12(3):3642-3653. doi: 10.1021/acsami.9b19614. Epub 2020 Jan 13.

DOI:10.1021/acsami.9b19614
PMID:31894955
Abstract

This study reports the superior performance of novel carbonaceous materials, CeO-encapsulated nitrogen-doped biochars [BC-Ce- ( = 1 and 2)], for oxygen reduction reaction (ORR). The biomass precursor of this value-added biochar material was biomimetically prepared via a hydroponic operation in the Ce-enriched solution. The characterization results showed that CeO with large amounts of oxygen vacancies was stably embedded in the N self-doped biochars during the pyrolytic processes. The measured specific surface areas of cerium-free biochar (BC sample), BC-Ce-1, and BC-Ce-2 were 79, 566, and 518 m/g, respectively. The BC-Ce- ( = 1 and 2) showed excellent ORR performances with onset potentials of ∼0.90-0.91 V, which outperformed the commercial 10 wt % Pt/C and BC. Compared with Pt/C, the BC-Ce-2 had better methanol tolerance and stability. Also, BC-Ce-2 displayed excellent electrochemical activity for Zn/air batteries. Controlled experiments and density functional theoretical calculations illustrated the synergistic effect between the pyri-N/C centers and CeO with oxygen vacancies in ORR. The Lewis base sites, created by pyri-N and oxygen vacancies, greatly facilitated the chemisorption of O molecules.

摘要

这项研究报告了新型碳质材料——CeO 封装的氮掺杂生物炭 [BC-Ce-(=1 和 2)] 在氧还原反应(ORR)中的卓越性能。这种增值生物炭材料的生物质前体是通过在富含铈的溶液中进行水培操作仿生制备的。表征结果表明,CeO 中的大量氧空位在热解过程中稳定地嵌入到 N 自掺杂生物炭中。未添加 Ce 的生物炭(BC 样品)、BC-Ce-1 和 BC-Ce-2 的比表面积分别为 79、566 和 518 m2/g。BC-Ce-(=1 和 2)表现出优异的 ORR 性能,起始电位约为 0.90-0.91 V,优于商业 10wt%Pt/C 和 BC。与 Pt/C 相比,BC-Ce-2 具有更好的甲醇耐受性和稳定性。此外,BC-Ce-2 还显示出对锌/空气电池优异的电化学活性。对照实验和密度泛函理论计算说明了在 ORR 中吡咯-N/C 中心与具有氧空位的 CeO 之间的协同效应。吡咯-N 和氧空位产生的Lewis 碱位极大地促进了 O 分子的化学吸附。

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