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Binary and ternary doping of nitrogen, boron, and phosphorus into carbon for enhancing electrochemical oxygen reduction activity

机译:将氮,硼和磷二元和三元掺杂到碳中以增强电化学氧还原活性

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摘要

N-doped carbon, a promising alternative to Pt catalyst for oxygen reduction reactions (ORRs) in acidic media, is modified in order to increase its catalytic activity through the additional doping of B and P at the carbon growth step. This additional doping alters the electrical, physical, and morphological properties of the carbon. The B-doping reinforces the sp ~2-structure of graphite and increases the portion of pyridinic-N sites in the carbon lattice, whereas P-doping enhances the charge delocalization of the carbon atoms and produces carbon structures with many edge sites. These electrical and physical alternations of the N-doped carbon are more favorable for the reduction of the oxygen on the carbon surface. Compared with N-doped carbon, B,N-doped or P,N-doped carbon shows 1.2 or 2.1 times higher ORR activity at 0.6 V (vs RHE) in acidic media. The most active catalyst in the reaction is the ternary-doped carbon (B,P,N-doped carbon), which records -6.0 mA/mg of mass activity at 0.6 V (vs RHE), and it is 2.3 times higher than that of the N-doped carbon. These results imply that the binary or ternary doping of B and P with N into carbon induces remarkable performance enhancements, and the charge delocalization of the carbon atoms or number of edge sites of the carbon is a significant factor in deciding the oxygen reduction activity in carbon-based catalysts.
机译:为了在酸性介质中进行氧还原反应(ORR)的Pt催化剂的一种有前途的替代方法,对N掺杂的碳进行了改性,以通过在碳生长步骤中对B和P进行额外的掺杂来提高其催化活性。这种额外的掺杂会改变碳的电,物理和形态学性质。 B掺杂增强了石墨的sp〜2-结构,并增加了碳晶格中吡啶N部位的部分,而P掺杂则增强了碳原子的电荷离域并产生了具有许多边缘部位的碳结构。 N掺杂碳的这些电学和物理的交替对于减少碳表面上的氧更有利。与N掺杂的碳相比,B,N掺杂或P,N掺杂的碳在酸性介质中在0.6 V(vs RHE)下的ORR活性高1.2或2.1倍。反应中活性最高的催化剂是三元掺杂碳(B,P,N掺杂碳),在0.6 V(vs RHE)下记录的质量活度为-6.0 mA / mg,是该值的2.3倍。 N掺杂碳。这些结果表明,将B和P与N进行二元或三元掺杂会显着提高性能,并且碳原子的电荷离域或碳边缘位置的数量是决定碳中氧还原活性的重要因素。基催化剂。

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