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核氧化非晶态钴磷纳米结构:一种先进且高效的析氧催化剂。

Core-Oxidized Amorphous Cobalt Phosphide Nanostructures: An Advanced and Highly Efficient Oxygen Evolution Catalyst.

作者信息

Anantharaj Sengeni, Reddy Pula Nagesh, Kundu Subrata

机构信息

Academy of Scientific and Innovative Research, CSIR-Central Electrochemical Research Institute (CECRI) Campus , New Delhi, India.

Electrochemical Materials Science (ECMS) Division, CSIR-CECRI , Karaikudi 630006, Tamil Nadu, India.

出版信息

Inorg Chem. 2017 Feb 6;56(3):1742-1756. doi: 10.1021/acs.inorgchem.6b02929. Epub 2017 Jan 24.

DOI:10.1021/acs.inorgchem.6b02929
PMID:28117987
Abstract

We demonstrated a high-yield and easily reproducible synthesis of a highly active oxygen evolution reaction (OER) catalyst, "the core-oxidized amorphous cobalt phosphide nanostructures". The rational formation of such core-oxidized amorphous cobalt phosphide nanostructures was accomplished by homogenization, drying, and annealing of a cobalt(II) acetate and sodium hypophosphite mixture taken in the weight ratio of 1:10 in an open atmosphere. Electrocatalytic studies were carried out on the same mixture and in comparison with commercial catalysts, viz., CoO-Sigma, NiO-Sigma, and RuO-Sigma, have shown that our catalyst is superior to all three commercial catalysts in terms of having very low overpotential (287 mV at 10 mA cm), lower Tafel slope (0.070 V dec), good stability upon constant potential electrolysis, and accelerated degradation tests along with a significantly higher mass activity of 300 A g at an overpotential of 360 mV. The synergism between the amorphous CoP shell with the CoO core is attributed to the observed enhancement in the OER performance of our catalyst. Moreover, detailed literature has revealed that our catalyst is superior to most of the earlier reports.

摘要

我们展示了一种高产且易于重现的合成高活性析氧反应(OER)催化剂“核心氧化非晶态磷化钴纳米结构”的方法。这种核心氧化非晶态磷化钴纳米结构的合理形成是通过在开放气氛中对醋酸钴和次磷酸钠按重量比1:10混合的混合物进行均质化、干燥和退火来实现的。对同一混合物进行了电催化研究,并与商业催化剂(即CoO-Sigma、NiO-Sigma和RuO-Sigma)进行了比较,结果表明,我们的催化剂在过电位非常低(10 mA cm时为287 mV)、塔菲尔斜率较低(0.070 V dec)、恒电位电解时稳定性良好、加速降解测试以及在360 mV过电位下具有显著更高的300 A g质量活性方面优于所有三种商业催化剂。非晶态CoP壳层与CoO核心之间的协同作用归因于我们催化剂的OER性能所观察到的增强。此外,详细的文献表明,我们的催化剂优于大多数早期报道。

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引用本文的文献

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Polymers (Basel). 2019 May 8;11(5):828. doi: 10.3390/polym11050828.
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Catalysis by design: development of a bifunctional water splitting catalyst through an operando measurement directed optimization cycle.
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Chem Sci. 2018 May 8;9(24):5322-5333. doi: 10.1039/c8sc01415a. eCollection 2018 Jun 28.