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担载在氮掺杂还原氧化石墨烯上的 CoO 纳米粒子作为用于 HO 还原、氧还原和析氧反应的多功能催化剂。

CoO nanoparticles anchored on nitrogen-doped reduced graphene oxide as a multifunctional catalyst for HO reduction, oxygen reduction and evolution reaction.

机构信息

Department of Chemistry, Capital Normal University, Beijing, 100048, China.

出版信息

Sci Rep. 2017 Mar 8;7:43638. doi: 10.1038/srep43638.

DOI:10.1038/srep43638
PMID:28272415
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5341290/
Abstract

This study describes a facile and effective route to synthesize hybrid material consisting of CoO nanoparticles anchored on nitrogen-doped reduced graphene oxide (CoO/N-rGO) as a high-performance tri-functional catalyst for oxygen reduction reaction (ORR), oxygen evolution reaction (OER) and HO sensing. Electrocatalytic activity of CoO/N-rGO to hydrogen peroxide reduction was tested by cyclic voltammetry (CV), linear sweep voltammetry (LSV) and chronoamperometry. Under a reduction potential at -0.6 V to HO, this constructing HO sensor exhibits a linear response ranging from 0.2 to 17.5 mM with a detection limit to be 0.1 mM. Although CoO/rGO or nitrogen-doped reduced graphene oxide (N-rGO) alone has little catalytic activity, the CoO/N-rGO exhibits high ORR activity. The CoO/N-rGO hybrid demonstrates satisfied catalytic activity with ORR peak potential to be -0.26 V (vs. Ag/AgCl) and the number of electron transfer number is 3.4, but superior stability to Pt/C in alkaline solutions. The same hybrid is also highly active for OER with the onset potential, current density and Tafel slope to be better than Pt/C. The unusual catalytic activity of CoO/N-rGO for hydrogen peroxide reduction, ORR and OER may be ascribed to synergetic chemical coupling effects between CoO, nitrogen and graphene.

摘要

这项研究描述了一种简便有效的方法,用于合成由 CoO 纳米粒子锚定在氮掺杂还原氧化石墨烯(CoO/N-rGO)上的混合材料,作为一种高性能的三功能催化剂,用于氧还原反应(ORR)、氧析出反应(OER)和 HO 传感。通过循环伏安法(CV)、线性扫描伏安法(LSV)和计时电流法测试了 CoO/N-rGO 对过氧化氢还原的电催化活性。在 -0.6 V 至 HO 的还原电位下,该构建的 HO 传感器在 0.2 至 17.5 mM 的范围内呈现出线性响应,检测限为 0.1 mM。尽管 CoO/rGO 或氮掺杂还原氧化石墨烯(N-rGO)单独的催化活性很小,但 CoO/N-rGO 表现出高的 ORR 活性。CoO/N-rGO 杂化具有满意的 ORR 活性,其 ORR 峰电位为-0.26 V(相对于 Ag/AgCl),电子转移数为 3.4,但在碱性溶液中比 Pt/C 更稳定。相同的杂化也对 OER 具有高活性,其起始电位、电流密度和塔菲尔斜率优于 Pt/C。CoO/N-rGO 对过氧化氢还原、ORR 和 OER 的异常催化活性可能归因于 CoO、氮和石墨烯之间的协同化学耦合效应。

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