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钴铁磷纳米片阵列作为一种用于析氧反应的高度协同且高效的电催化剂。

Co-Fe-P Nanosheet Arrays as a Highly Synergistic and Efficient Electrocatalyst for Oxygen Evolution Reaction.

作者信息

Xie Yanyu, Huang Huanfeng, Chen Zhuodi, He Zhujie, Huang Zhixiang, Ning Shunlian, Fan Yanan, Barboiu Mihail, Shi Jian-Ying, Wang Dawei, Su Cheng-Yong

机构信息

Lehn Institute of Functional Materials, MOE Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China.

Institut Europeen des Membranes, Adaptive Supramolecular Nanosystems Group, University of Montpellier, ENSCM-CNRS, Place E. Bataillon CC047, 34095 Montpellier, France.

出版信息

Inorg Chem. 2022 May 30;61(21):8283-8290. doi: 10.1021/acs.inorgchem.2c00727. Epub 2022 May 18.

Abstract

The rational design and synthesis of highly efficient electrocatalysts for oxygen evolution reaction (OER) is of critical importance to the large-scale production of hydrogen by water electrolysis. Here, we develop a bimetallic, synergistic, and highly efficient Co-Fe-P electrocatalyst for OER, by selecting a two-dimensional metal-organic framework (MOF) of Co-ZIF-L as the precursor. The Co-Fe-P electrocatalyst features pronounced synergistic effects induced by notable electron transfer from Co to Fe, and a large electrochemical active surface area achieved by organizing the synergistic Co-Fe-P into hierarchical nanosheet arrays with disordered grain boundaries. Such features facilitate the generation of abundant and efficiently exposed Co sites for electrocatalytic OER and thus enable Co-Fe-P to deliver excellent activity (overpotential and Tafel slope as low as 240 mV and 36 mV dec, respectively, at a current density of 10 mA cm in 1.0 M KOH solution). The Co-Fe-P electrocatalyst also shows great durability by steadily working for up to 24 h. Our work thus provides new insight into the development of highly efficient electrocatalysts based on nanoscale and/or electronic structure engineering.

摘要

合理设计和合成用于析氧反应(OER)的高效电催化剂对于通过水电解大规模制氢至关重要。在此,我们通过选择二维Co-ZIF-L金属有机框架(MOF)作为前驱体,开发了一种用于OER的双金属、协同且高效的Co-Fe-P电催化剂。Co-Fe-P电催化剂具有显著的协同效应,这是由从Co到Fe的显著电子转移引起的,并且通过将协同的Co-Fe-P组织成具有无序晶界的分级纳米片阵列实现了大的电化学活性表面积。这些特性有助于产生大量且有效暴露的用于电催化OER的Co位点,从而使Co-Fe-P具有优异的活性(在1.0 M KOH溶液中,电流密度为10 mA cm时,过电位和塔菲尔斜率分别低至240 mV和36 mV dec)。Co-Fe-P电催化剂还通过稳定工作长达24小时表现出出色的耐久性。因此,我们的工作为基于纳米尺度和/或电子结构工程的高效电催化剂的开发提供了新的见解。

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