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氮掺杂碳纳米壁/金刚石薄膜作为氧还原反应的高效电催化剂。

Nitrogen-doped carbon nanowalls/diamond films as efficient electrocatalysts toward oxygen reduction reaction.

作者信息

Zhang Chuyan, Huang Nan, Zhai Zhaofeng, Liu Lusheng, Chen Bin, Lu Zhigang, Zhou Meiqi, Song Haozhe, Shi Dan, Yang Bing, Yang Nianjun, Jiang Xin

机构信息

Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, No.72 Wenhua Road, Shenyang 110016, People's Republic of China.

Institute of Materials Engineering, University of Siegen, No.9-11 Paul-Bonatz-Str., Siegen D-57076, Germany.

出版信息

Nanotechnology. 2021 Oct 20;33(1). doi: 10.1088/1361-6528/ac2a84.

DOI:10.1088/1361-6528/ac2a84
PMID:34571493
Abstract

Substitution of commercial Pt/C electrocatalysts with efficient carbon-based ones for oxygen reduction reaction (ORR) still remains a huge challenge. For practical ORR applications it is significant to design robust 3D network nanostructures in that they do not require polymer binders. For conventional powder catalysts, they must be combined with substrate, leading to their shedding and degradation. In this work, vertically-aligned N-doped carbon nanowalls/diamond (N-CNWs/D) films are synthesized by means of a microwave plasma chemical vapor deposition technique, where nitrogen doping is conducted during the growth process and a subsequent facile annealing treatment under Ar atmosphere. The obtained Ar treated N-CNWs/D film exhibits an ORR onset potential of 835 mV (versus reversible hydrogen electrode) in 0.1 mol lKOH solution in a four-electron reaction pathway. It also displays excellent tolerance toward methanol crossover and long-term stability (e.g. a current density loss of only 10% even after 16 h measurement). The boosting ORR performance can be attributed to the activated pyridinic N dopant at abundant edge sites and enlarged electrochemical surface areas of N-CNWs/D films. This work not only develops a controllable strategy to fabricate binder-free carbon-based ORR electrocatalysts, but also paves a way to in-depth understand actual active sites in terms of ORR pathway mechanisms.

摘要

用高效的碳基催化剂替代商业铂碳(Pt/C)电催化剂用于氧还原反应(ORR)仍然是一个巨大的挑战。对于实际的ORR应用来说,设计坚固的三维网络纳米结构非常重要,因为它们不需要聚合物粘合剂。对于传统的粉末催化剂,它们必须与基底结合,这会导致其脱落和降解。在这项工作中,通过微波等离子体化学气相沉积技术合成了垂直排列的氮掺杂碳纳米壁/金刚石(N-CNWs/D)薄膜,其中在生长过程中进行氮掺杂,并随后在氩气气氛下进行简便的退火处理。所获得的经氩气处理的N-CNWs/D薄膜在0.1 mol lKOH溶液中以四电子反应途径表现出835 mV(相对于可逆氢电极)的ORR起始电位。它还对甲醇渗透表现出优异的耐受性和长期稳定性(例如,即使在测量16小时后电流密度损失仅为10%)。ORR性能的提升可归因于在丰富边缘位点处被激活的吡啶型氮掺杂剂以及N-CNWs/D薄膜增大的电化学表面积。这项工作不仅开发了一种可控策略来制备无粘合剂的碳基ORR电催化剂,而且为从ORR途径机制方面深入理解实际活性位点铺平了道路。

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