MoS2 Anchored on Agar-Derived 3D Nitrogen-Doped Porous Carbon for Electrocatalytic Hydrogen Evolution Reaction and Lithium-Ion Batteries

被引:6
|
作者
Cao, Chunling [1 ]
Liu, Shengkai [1 ]
Fan, Jinxin [1 ]
Li, Guodong [2 ]
Arenal, Raul [2 ]
Wang, Cheng [1 ]
Li, Wenjiang [1 ]
Xie, Fei [1 ]
机构
[1] Tianjin Univ Technol, Sch Mat Sci & Engn, Sch Chem & Chem Engn, Tianjin Key Lab Organ Solar Cells & Photochem Con, Tianjin 300384, Peoples R China
[2] Univ Zaragoza, CSIC, Inst Nanociencia & Mat Aragon INMA, Calle Mariano Esquillor, Zaragoza 50018, Spain
来源
ADVANCED SUSTAINABLE SYSTEMS | 2022年 / 6卷 / 03期
基金
中国国家自然科学基金;
关键词
hydrogen evolution reaction; lithium-ion batteries; molybdenum disulfide; nitrogen-doped porous carbon; ENERGY-STORAGE; ELECTROCHEMICAL PROPERTIES; PERFORMANCE; NANOSHEETS; ANODE; FRAMEWORKS; EXCELLENT; SPHERES; SULFUR; RICH;
D O I
10.1002/adsu.202100393
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
MoS2 has been explored as a potential material for hydrogen evolution reaction (HER) and lithium-ion batteries (LIBs). However, the limited number of active sites and poor conductivity restrain its applications. Herein, a facile method is reported to construct MoS2 nanosheets (MoS(2)NSs) grown on agar-derived 3D nitrogen-doped porous carbon (MoS2-NPC). The as-prepared MoS2-NPC composite exhibits good stability and HER electrocatalytic properties with a low overpotential of 209 mV at 10 mA cm(-2) and a small Tafel slope of 41 mV dec(-1). Furthermore, as an anode of LIBs, it delivers an initial discharge capacity of 1289 mAh eat 0.1 A g(-1) and rate capability of 712 and 419 mAh g(-1) at 0.5 and 2.0 A g(-1), respectively. This is attributed to the synergistic effects and unique 3D network structure, which avoids the aggregation of MoS2 and results in more exposed active sites. The agar-derived 3D nitrogen-doped porous carbon can act as a support material for MoS(2)NSs dispersed on the surface, providing a cheap and efficient strategy to prepare high quality catalysts for electrochemical energy conversion and storage applications.
引用
收藏
页数:10
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