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近球形的磷酸钴纳米颗粒/碳纳米片杂化物:一种用于氧还原和水分解的高性能三功能电催化剂。

Nearly spherical CoP nanoparticle/carbon nanosheet hybrids: a high-performance trifunctional electrocatalyst for oxygen reduction and water splitting.

作者信息

Zou Wenjian, Dou Kunpeng, Jiang Qi, Xiang Jiadong, Kaun Chao-Cheng, Tang Hao

机构信息

State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology Wuhan 430070 People's Republic of China

College of Information Science and Engineering, Ocean University of China Qingdao 266100 People's Republic of China.

出版信息

RSC Adv. 2019 Dec 4;9(68):39951-39957. doi: 10.1039/c9ra07334e. eCollection 2019 Dec 2.

Abstract

Developing active multifunctional electrocatalysts composed of earth-abundant and cheap elements is an urgent demand in energy conversion applications. This study presents a facile approach for the scalable synthesis of nanostructured cobalt phosphide embedded in carbon nanosheets (CoP NPs/CNSs). The hybrid structures show highly efficient trifunctional electrocatalytic activities toward the oxygen reduction reaction (ORR), oxygen evolution reaction (OER), and hydrogen evolution reaction (HER) under alkaline condition. The catalytic performances, which are remarkably superior to those of the previously reported CoP nanostructures enclosed by single or a few low index facets, can be attributed to the nearly spherical shape of the CoP nanoparticles with many more exposed crystal planes. Density functional theory (DFT) computations are performed to investigate the facet effects of CoP on electrocatalytic activity, and they reveal the relatively low overpotentials of (101) facets towards the OER and the free energy of water dissociation (Δ ) and adsorbed H intermediates (Δ ) of (311) toward the HER being close to thermoneutral. This work is expected to inspire the design and fabrication of multifunctional and high-efficiency electrocatalysts by selectively exposing specific crystal planes.

摘要

开发由储量丰富且廉价的元素组成的活性多功能电催化剂是能源转换应用中的迫切需求。本研究提出了一种简便的方法,用于可扩展地合成嵌入碳纳米片的纳米结构磷化钴(CoP NPs/CNSs)。该混合结构在碱性条件下对氧还原反应(ORR)、析氧反应(OER)和析氢反应(HER)表现出高效的三功能电催化活性。其催化性能明显优于先前报道的由单个或几个低指数晶面包围的CoP纳米结构,这可归因于具有更多暴露晶面的近球形CoP纳米颗粒。进行密度泛函理论(DFT)计算以研究CoP的晶面效应,结果表明(101)晶面对OER的过电位相对较低,(311)晶面对HER的水解离自由能(Δ )和吸附H中间体的自由能(Δ )接近热中性。这项工作有望通过选择性暴露特定晶面来激发多功能高效电催化剂的设计与制备。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4870/9076228/93d0d458d142/c9ra07334e-f1.jpg

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