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Prof. Dr. Xuebo Zhao
Qilu University of Technology
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Current Location :> Home > Publications > Text
One-step and scalable synthesis of Ni2P nanocrystals encapsulated in N, P-codoped hierarchically porous carbon matrix using a bipyridine and phosphonate linked nickel metal-organic framework as highly efficient electrocatalysts for overall water splitting,
writer:Liting Yan,Huimin Jiang,Ying Wang,Liangjun Li,Xin Gu,Pengcheng Dai,Dandan Liu,Si-Fu Tang,Xuebo Zhao*
keywords:Metal-organic frameworks;One-step pyrolysis;Multi-component doping;electrocatalyst;Nickel phosphides;Overall water splitting
source:期刊
specific source:ELECTROCHIMICA ACTA,2019 ,297 , pp.755-766
Issue time:2019年
The development of highly active and durable noble-metal-free electrocatalysts for overall water splitting is a great challenge. Herein, a microdroplet flow reaction is used for ultrafast and continuous synthesis of a nickel metal-organic framework material with 4,4''-bipyridine and phosphonate ligands. A one step pyrolysis of this metal-organic framework to various heat treatment temperatures and hold times at maximum temperature give a range of electrocatalysts, containing crystalline Ni2P nanoparticles dispersed in a porous carbonaceous matrix incorporating relatively high concentrations of both nitrogen and phosphorus derived from the original metaleorganic framework. The Ni2P electrocatalysts inherite the morphology of the metal-organic framework precursor, have a uniform dispersion of Ni2P sites and Brunauer-Emmett-Teller surface areas in the range 558-754 m(2) g(-1). The Ni2P electrocatalysts exhibit excellent catalytic performance for both hydrogen and oxygen evolution reactions in 1.0 M KOH and an electrolyzer using Ni2P electrocatalysts as both cathode and anode generates a current density of 10 mA cm(-2) at a voltage of 1.62 V with superior durability. This facile and scalable synthesis strategy for the rational design of electrocatalysts represents a proof-of-concept with the potential for scale-up for use in practical applications. (C) 2018 Elsevier Ltd. All rights reserved.
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