共 50 条
Fabricating carbon quantum dots of graphitic carbon nitride vis ultrasonic exfoliation for highly efficient H2O2 production
被引:21
|作者:
Wang, Yue
[1
,2
]
Yang, Zhaojing
[1
]
Zhang, Chengxu
[1
]
Feng, Yuebin
[3
]
Shao, Haodong
[1
,2
]
Chen, Jian
[1
]
Hu, Jue
[1
,2
]
Zhang, Libo
[1
,2
]
机构:
[1] Kunming Univ Sci & Technol, Fac Met & Energy Engn, Kunming 650093, Peoples R China
[2] Kunming Univ Sci & Technol, State Key Lab Complex Nonferrous Met Resources Cle, Kunming 650093, Yunnan, Peoples R China
[3] Kunming Univ Sci & Technol, Fac Sci, Kunming 650093, Peoples R China
关键词:
Graphitic carbon nitride;
Ultrasound;
Two-electron oxygen reduction;
Hydrogen peroxide preparation;
NANOSHEETS;
PHOTOCATALYSTS;
PERFORMANCE;
CHEMISTRY;
D O I:
10.1016/j.ultsonch.2023.106582
中图分类号:
O42 [声学];
学科分类号:
070206 ;
082403 ;
摘要:
A promising and sustainable approach for producing hydrogen peroxide is the two-electron oxygen reduction reaction (2e- ORR), which uses very stable graphitic carbon nitride (g-C3N4). However, the catalytic performance of pristine g-C3N4 is still far from satisfactory. Here, we demonstrate for the first time the controlled fabrication of carbon quantum dots (CQDs)-modified graphitic carbon nitride carbon (g-C3N4/CQDs-X) by ultrasonic stripping for efficient 2e- ORR electrocatalysis. HRTEM, UV-vis, EPR and EIS analyses are in good consistent which prove the in-situ generation of CQDs. The effect of sonication time on the physical properties and ORR activity of g-C3N4 is discussed for the first time. The g-C3N4/CQDs-12 catalyst shows a selectivity of up to 95% at a potential of 0.35 V vs. RHE, which is much higher than that of the original g-C3N4 catalyst (88%). Additionally, the H2O2 yield is up to 1466.6 mmol g-1 in 12 h, which is twice as high as the original g-C3N4 catalyst. It is discovered that the addition of CQDs through ultrasonic improves the g-C3N4 catalyst's electrical conductivity and electron transfer capability in addition to its high specific surface area and distinctive porous structure, speeding up the reaction rate. This research offers a green method for enhancing g-C3N4 activity.
引用
收藏
页数:12
相关论文