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原位生长的碳球作为钴氧化物在氧析出反应中增强活性的理想载体。

In-situ developed carbon spheres function as promising support for enhanced activity of cobalt oxide in oxygen evolution reaction.

机构信息

Department of Chemistry, BITS Pilani, Pilani, Rajasthan 333031, India.

出版信息

J Colloid Interface Sci. 2018 Nov 15;530:264-273. doi: 10.1016/j.jcis.2018.06.087. Epub 2018 Jun 28.

Abstract

Highly active, stable electrocatalyst for oxygen evolution reaction (OER) is sincerely required for the practical application of water splitting to get rid from the sluggish reaction kinetics and the stability issue. Here, CoO is studied as OER catalyst and to improve the electrocatalytic activity, carbon is chosen as the conducting support. A simple and cost-effective synthetic route is developed for the synthesis of CoO on carbon support following hydrothermal route using various hydrolyzing agents. The heterostructure 'CoO/C' perform well in OER as a non-precious metal catalyst. The best CoO/C electrocatalyst can generate 10 and 30 mA/cm current densities upon application of 1.623 V and 1.678 V vs. RHE whereas, bare CoO can generate current density of 10 and 30 mA/cm upon application of 1.677 and 1.754 V vs. RHE. Carbon in the heterostructure helps to improve the conductivity and at the same time enhances the charge transfer ability which further leads to increase current density and stability to the catalyst. CoO/C can generate unaltered current density up to 1000 cycles.

摘要

对于水分解的实际应用,需要高效、稳定的析氧反应 (OER) 电催化剂来摆脱缓慢的反应动力学和稳定性问题。在这里,CoO 被研究为 OER 催化剂,为了提高电催化活性,选择碳作为导电载体。通过水热法,使用各种水解剂,开发了一种简单且具有成本效益的合成 CoO 负载在碳载体上的方法。异质结构 'CoO/C' 作为非贵金属催化剂在 OER 中表现良好。最佳的 CoO/C 电催化剂在施加 1.623 V 和 1.678 V 相对于 RHE 时可分别产生 10 和 30 mA/cm 的电流密度,而纯 CoO 在施加 1.677 和 1.754 V 相对于 RHE 时可分别产生 10 和 30 mA/cm 的电流密度。异质结构中的碳有助于提高导电性,同时增强电荷转移能力,从而进一步提高催化剂的电流密度和稳定性。CoO/C 可以在 1000 个循环内产生不变的电流密度。

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