Nickel-Rich Phosphide (Ni12P5) Nanosheets Coupled with Oxidized Multiwalled Carbon Nanotubes for Oxygen Evolution

被引:31
作者
Aziz, S. K. Tarik [1 ]
Malik, Bibhudatta [1 ]
Sadhanala, Hari Krishna [1 ]
Gedanken, Aharon [1 ]
Noked, Malachi [1 ]
Nessim, Gilbert Daniel [1 ]
机构
[1] Bar Ilan Univ, Bar Ilan Inst Nanotechnol & Adv Mat BINA, Dept Chem, IL-52900 Ramat Gan, Israel
基金
以色列科学基金会;
关键词
nickel phosphide; mildly oxidized multiwalled carbon nanotubes; oxygen evolution reaction; X-ray photoelectron spectroscopy; chronoamperometry; ELECTROCHEMICAL WATER OXIDATION; CATALYTIC-ACTIVITY; FACILE SYNTHESIS; OXIDE; EFFICIENT; ELECTROCATALYSTS; CRYSTALLIZATION; NANOPARTICLES; STABILITY; HYDROGEN;
D O I
10.1021/acsanm.0c02169
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Exploring and identifying efficient materials with operative active sites for electrochemical oxygen evolution reaction (OER) is of paramount importance for the future of energy conversion technologies like electrolyzers and fuel cells. Herein, we develop an effective strategy to couple physically distinct metal-rich nickel phosphide (Ni12P5) with mildly oxidized multiwall carbon nanotubes (O-MWCNTs) to boost the efficiency of OER. Ni12P5-O-MWCNTs outperforms O-2 evolution activity in contrast to the parental materials, Ni12P5 and O-MWCNTs. Intriguingly, Ni12P5-O-MVVCNTs shows an overpotential of 280 mV achieved at a current density of 10 mAcm(-2). The hybrid, Ni12P5-O-MWCNTs demonstrates remarkable OER activity by the virtue of development of heterointerfaces in which the effective interaction between Ni12P5 and O-MWCNTs plays a crucial role. Moreover, we have analyzed the XPS and HR-TEM of Ni12P5-O-MWCNTs after the chronoamperometry study of OER to examine the structural changes due to the prolonged oxidation reaction. This post OER study enabled us to identify the precatalyst and the active functional groups present in O-MWCNTs. Our approach opens a path for fabricating hybrid catalytic systems with synergetic activity to facilitate optimized electrocatalytic activity.
引用
收藏
页码:10914 / 10921
页数:8
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