OH-enriched NiS/Ni3S2-Zr Heterostructure for Overall Water Splitting Performance in Alkaline Media

被引:3
|
作者
Sai, K. Naga Sathya [1 ]
Darsan, Ardra S. [2 ,3 ]
Wang, Kehan [1 ]
Pandikumar, Alagarsamy [3 ,4 ]
Venkatakrishnan, Shankar Muthukonda [5 ]
Hong, Zhanglian [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, Hangzhou 310027, Peoples R China
[2] Cent Electrochem Res Inst, Electrochem Power Sources Div, CSIR, Karaikkudi 630003, Tamil Nadu, India
[3] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[4] Cent Electrochem Res Inst, Electroorgan & Mat Electrochem Div, CSIR, Karaikkudi 630003, Tamil Nadu, India
[5] Yogi Vemana Univ, Dept Mat Sci & Nanotechnol, Nanocatalysis & Solar Fuels Res Lab, Kadapa 516005, Andhra Pradesh, India
关键词
NiS/Ni3S2; OH-groups; doping; bifunctional electrocatalyst; porousheterostructure; water splitting; green hydrogen; HYDROGEN EVOLUTION REACTION; NITROGEN-DOPED GRAPHENE; NANOSHEET ARRAYS; NICKEL FOAM; EFFICIENT; ELECTROCATALYST; ELECTRODE;
D O I
10.1021/acsanm.4c01502
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The development of highly efficient Ni-sulfide-based catalysts is desirable but limited due to slow kinetics in alkaline hydrogen evolution reactions (HER) and water electrolysis. Herein, we report the design of a high-valent doping strategy combined with selective surface etching to generate an OH-enriched porous heterostructure NiS/Ni3S2 nanosphere with an optimal electronic structure. The E-NiS/Ni3S2-Zr-(6 mM) electrocatalyst requires only 50 mV to achieve 10 mA cm(-2) for the HER. Oxygen evolution reaction (OER) requires 205 and 282 mV to reach 10 and 100 mA cm(-2), respectively. In addition, for total water splitting in alkaline medium, the assembled cell with E-NiS/Ni3S2-Zr-(6 mM) as both the positive and negative electrodes requires ultralow voltages of 1.41 and 1.51 V at 10 mA and 20 mA cm(-2) current densities, respectively. Notably, E-NiS/Ni3S2-Zr-(6 mM) showed excellent stability for 30 h in HER, OER, and water electrolysis. Delving into the underlying electrochemical processes and electron transfer kinetics, a diverse array of techniques such as linear sweep voltammogram, electrochemical impedance spectroscopy, electrochemical active surface area, C-dl, cyclic voltammetry, chronoamperometric, and turn over frequency were employed. Comprehensive characterization encompassing X-ray diffraction, X-ray photoelectron spectroscopy, Fourier transform infrared, Raman, scanning electron microscopy, energy dispersive X-ray spectroscopy, and transmission electron microscopy was conducted to explore the electronic and morphological attributes of the synthesized materials. The approach formulated in this study paves the way for achieving optimal electrocatalyst performance, positioning them as compelling alternatives to noble metal-based electrocatalysts.
引用
收藏
页码:11931 / 11941
页数:11
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