Metal organic framework nanosheets in-situ derivatization of heterogeneous Cu2S/Ni3S2 nanoparticles for enhanced water splitting and glucose sensing

被引:6
作者
Jiang, Rong [1 ]
Cheng, Yikun [1 ]
Wang, Tianshuo [1 ]
Zhu, Youqi [2 ]
Cao, Chuanbao [2 ]
Ma, Xiaojun [1 ]
Liu, Guohan [3 ]
Chen, Long [1 ]
机构
[1] Shihezi Univ, Sch Chem & Chem Engn, State Key Lab Incubat,Base Green Proc Chem Engn, Shihezi 832003, Peoples R China
[2] Beijing Inst Technol, Res Ctr Mat Sci, Beijing Key Lab Construct Tailorable Adv Funct Mat, Beijing 100081, Peoples R China
[3] Gansu Acad Sci, Inst Sensor Technol, Lanzhou 730000, Peoples R China
关键词
MOFs; Heterogeneous; Water splitting; Glucose detection; HYDROGEN EVOLUTION; HIGHLY EFFICIENT; ALKALINE; ARRAYS; ELECTROCATALYSTS; MODULATION; SURFACE; FOAM; NI;
D O I
10.1016/j.ijhydene.2023.06.322
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metal organic frameworks (MOFs) are considered as promising electrocatalytic materials because of its good designability and structural diversity. Herein, the composite materials of Cu2S/Ni3S2@Ni-BDC/NF are successfully synthesized through the hydrothermal and electrodeposition methods. The distinctive heterostructure provides ample active sites and retains structural integrity to promote durability. When it is explored as bifunctional electrocatalyst, the overpotential of 63 mV at 10 mA cm-2 current density for the hydrogen evolution reaction (HER), the overpotential of 353 mV at 50 mA cm-2 current density for the oxygen evolution reaction (OER). In a two-electrode system, an extremely low cell voltage of 1.55 Vis required to achieve 20 mA cm-2 current density. Moreover, Cu2S/Ni3S2@Ni-BDC exhibits satisfactory glucose sensitivity of 56,220 mA mM-1 cm-2 and outstanding anti-interference performance. This design not only successfully constructs 0D/2D heterogeneous interface of electrocatalyst, but also demonstrates the multifunctional application potential of water splitting and glucose electrochemical sensors.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:647 / 657
页数:11
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