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CoO纳米颗粒在片状碳纳米纤维上的高分散性及氧还原反应活性。

High dispersion and oxygen reduction reaction activity of CoO nanoparticles on platelet-type carbon nanofibers.

作者信息

Yamada Naohito, Kowalski Damian, Koyama Akira, Zhu Chunyu, Aoki Yoshitaka, Habazaki Hiroki

机构信息

Faculty of Engineering, Hokkaido University Sapporo Hokkaido 060-8628 Japan

Graduate School of Chemical Sciences and Engineering, Hokkaido University Sapporo Hokkaido 060-8628 Japan.

出版信息

RSC Adv. 2019 Jan 28;9(7):3726-3733. doi: 10.1039/c8ra09898k. eCollection 2019 Jan 25.

Abstract

In this study, platelet-type carbon nanofibers prepared by the liquid phase carbonization of polymers in the pores of a porous anodic alumina template were used to prepare the CoO/carbon electrocatalysts. For comparison, CoO nanoparticles were also deposited on multiwall carbon nanotubes (MWCNTs). Both the nitrogen-free platelet-type carbon nanofibers (pCNFs) and the nitrogen-containing analogue (N-pCNFs) exhibited better dispersion and higher amount of deposited CoO nanoparticles compared to the MWCNTs. In addition, many individual CoO nanoparticles were deposited separately on pCNF and N-pCNF, whereas aggregated deposition was commonplace on MWCNTs. The results indicated that the side wall of the pCNFs, which consisted of carbon edge planes, was the preferential nucleation site of CoO nanoparticles rather than the basal planes of carbon that predominated the surface of the MWCNTs. The oxygen reduction reaction (ORR) activity of the CoO/pCNF composite in 0.1 mol dm KOH solution was better than that of CoO/MWCNTs. The N-pCNF further enhanced the ORR activity of the CoO/pCNFs even though the dispersion and supported amount of CoO nanoparticles were negligibly affected by the presence of the nitrogen species. Synergistic interactions of the CoO nanoparticles with N-doped CNFs contributed to the increased ORR activity.

摘要

在本研究中,通过在多孔阳极氧化铝模板的孔隙中对聚合物进行液相碳化制备的血小板型碳纳米纤维被用于制备CoO/碳电催化剂。为作比较,CoO纳米颗粒也被沉积在多壁碳纳米管(MWCNTs)上。与MWCNTs相比,无氮血小板型碳纳米纤维(pCNFs)和含氮类似物(N-pCNFs)均表现出更好的分散性以及更高的CoO纳米颗粒沉积量。此外,许多单个的CoO纳米颗粒分别沉积在pCNF和N-pCNF上,而在MWCNTs上则常见聚集沉积。结果表明,由碳边缘平面组成的pCNFs的侧壁是CoO纳米颗粒的优先成核位点,而非主导MWCNTs表面的碳基面。CoO/pCNF复合材料在0.1 mol dm KOH溶液中的氧还原反应(ORR)活性优于CoO/MWCNTs。尽管CoO纳米颗粒的分散性和负载量受氮物种存在的影响可忽略不计,但N-pCNF进一步提高了CoO/pCNFs的ORR活性。CoO纳米颗粒与氮掺杂CNFs的协同相互作用导致ORR活性增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5bbb/9060432/8fc1a9ecb4c8/c8ra09898k-f1.jpg

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