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Porous Carbon Nanosheets Codoped with Nitrogen and Sulfur for Oxygen Reduction Reaction in Microbial Fuel Cells

机译:氮和硫共掺杂的多孔碳纳米片在微生物燃料电池中的氧还原反应

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In this work, a simple synthesis strategy has been developed for the preparation of nitrogen and sulfur-codoped porous carbon nanosheets (N/S-CNS) as a cathode catalyst for microbial fuel cells (MFCs). The as-prepared N/S-CNS showed favorable features for electrochemical energy conversion such as high surface area (1004 m(2) g(-1)), defect structure, and abundant exposure of active sites that arose primarily from porous nanosheet morphology. Benefiting from the unique nanostructure, the resulting nanosheets exhibited effective electrocatalytic activity toward oxygen reduction reaction (ORR). The onset potential of the N/S-CNS in linear-sweep voltammetry was approximately -0.05 V vs Ag/AgCl in neutral phosphate buffer saline. Electrochemical impedance spectroscopy showed that the ohmic and charge-transfer resistance of the codoped catalyst were 1.5 and 14.8 Omega, respectively, both of which were lower than that of platinum/carbon (Pt/C). Furthermore, the electron-transfer number of the N/S-CNS was calculated to be similar to 3.5, suggesting that ORR on the catalyst proceeds predominantly through the favorable four-electron pathway. The MFC with N/S-CNS as a cathode catalyst generated current density (6.6 A m(-2)) comparable to that with Pt/C (7.3 A m(-2)). The high durability and low price indicate that N/S-CNS can be a competitive catalyst for applications of MFCs.
机译:在这项工作中,已经开发出一种简单的合成策略,用于制备氮和硫共掺杂的多孔碳纳米片(N / S-CNS),作为微生物燃料电池(MFCs)的阴极催化剂。所制备的N / S-CNS显示出电化学能量转换的有利功能,例如高表面积(1004 m(2)g(-1)),缺陷结构以及主要由多孔纳米片形态引起的大量活性位暴露。得益于独特的纳米结构,所得纳米片对氧还原反应(ORR)表现出有效的电催化活性。 N / S-CNS在线性扫描伏安法中的起始电位相对于在中性磷酸盐缓冲盐水中的Ag / AgCl约为-0.05V。电化学阻抗谱表明,共掺杂催化剂的欧姆电阻和电荷转移电阻分别为1.5和14.8Ω,均低于铂/碳(Pt / C)。此外,N / S-CNS的电子转移数经计算与3.5相似,表明催化剂上的ORR主要通过有利的四电子途径进行。使用N / S-CNS作为阴极催化剂的MFC产生的电流密度(6.6 A m(-2))与Pt / C(7.3 A m(-2))相当。高耐久性和低价格表明,N / S-CNS可以成为MFC应用的竞争催化剂。

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