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首页> 外文期刊>Electrochimica Acta >One-step synthesis of shell/core structural boron and nitrogen co-doped graphitic carbonanodiamond as efficient electrocatalyst for the oxygen reduction reaction in alkaline media
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One-step synthesis of shell/core structural boron and nitrogen co-doped graphitic carbonanodiamond as efficient electrocatalyst for the oxygen reduction reaction in alkaline media

机译:壳/核结构硼和氮共掺杂石墨碳/纳米金刚石的一步合成,作为碱性介质中氧还原反应的有效电催化剂

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Shell/core structural boron and nitrogen co-doped graphitic carbonanodiamond (BN-C/ND) non-noble metal catalyst has been synthesized by a simple one-step heat-treatment of the mixture with nanodiamond, melamine, boric acid and FeCl3. In the process of the surface graphitization of nanodiamond with catalysis by FeCl3, B and N atoms from the decomposition of boric acid and melamine were directly introduced into the graphite lattice to form B, N co-doped graphitic carbon shell, while the core still retained the diamond structure. Electrochemical measurements of the BN-C/ND catalyst show much higher electrocatalytic activities towards oxygen reduction reaction (ORR) in alkaline medium than its analogues doped with B or N alone (B-C/ND or N-C/ND). The high catalytic activity of BN-C/ND is attributed to the synergetic effect caused by co-doping of C/ND with B and N. Meanwhile, the BN-C/ND exhibits an excellent electrochemical stability due to the special shell/core structure. There is almost no alteration occurred in the cyclic voltammetry measurements for BN-C/ND before and after 5000 cycles. All experimental results prove that the BN-C/ND may be exploited as a potentially efficient and inexpensive non-noble metal cathode catalyst for ORR to substitute Pt-based catalysts in fuel cells. (C) 2016 Elsevier Ltd. All rights reserved.
机译:通过对纳米金刚石,三聚氰胺,硼酸和FeCl3进行简单的一步热处理,合成了壳/核结构硼和氮共掺杂的石墨碳/纳米金刚石(BN-C / ND)非贵金属催化剂。在FeCl3催化下的纳米金刚石表面石墨化过程中,硼酸和三聚氰胺分解产生的B和N原子被直接引入石墨晶格中,形成B,N共掺杂的石墨碳壳,而核仍保留钻石结构。 BN-C / ND催化剂的电化学测量表明,在碱性介质中,其对氧还原反应(ORR)的电催化活性远高于仅掺杂B或N的类似物(B-C / ND或N-C / ND)。 BN-C / ND的高催化活性归因于C / ND与B和N共同掺杂引起的协同效应。同时,BN-C / ND由于特殊的壳/核而具有出色的电化学稳定性。结构体。 5000次循环前后,BN-C / ND循环伏安法测量中几乎没有发生变化。所有实验结果证明,BN-C / ND可用作ORR的潜在有效且廉价的非贵金属阴极催化剂,以替代燃料电池中的Pt基催化剂。 (C)2016 Elsevier Ltd.保留所有权利。

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