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In situ modification of cobalt on MXene/TiO2 as composite photocatalyst for efficient nitrogen fixation
被引:84
|作者:
Gao, Wanguo
[1
]
Li, Xiaoman
[1
]
Luo, Shijian
[1
]
Luo, Zhenglong
[1
]
Zhang, Xu
[1
]
Huang, Rong
[1
]
Luo, Min
[1
]
机构:
[1] Ningxia Univ, Sch Chem & Chem Engn, State Key Lab High Efficiency Utilizat Coal & Gre, Yinchuan 750021, Ningxia, Peoples R China
基金:
中国国家自然科学基金;
关键词:
MXene;
TiO2;
Co-modified;
Photocatalytic nitrogen fixation;
CARBON NITRIDE;
OXYGEN VACANCIES;
001;
FACETS;
AMMONIA;
NANOSHEETS;
HETEROJUNCTION;
PHOTOFIXATION;
PERFORMANCE;
DINITROGEN;
REDUCTION;
D O I:
10.1016/j.jcis.2020.11.064
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:
Modulation of the binding of the reactant or product species with catalysts is an effective approach to optimize the photocatalytic activity. Herein, we explored the relationship between the binding of reactant (N-2) and product (NH3) with catalyst and the photocatalytic nitrogen fixation activity. The surface reactivity of nitrogen with water was tuned by introducing Co into the MXene@TiO2 catalysts, which the TiO2 nanoparticle derived from the in-situ growth on the surface of MXene nanosheets. Co modified adjusted the chemisorption equilibrium of the catalyst for reactant (N-2) and product (NH3), thus promoted product desorption and efficiency of the active site. Remarkably, the optimal catalyst (MXene/TiO2/Co-0.5%) exhibited outstanding NH4+ production rate (110 mu mol g(-1) h(-1)) and excellent stability in pure water without any hole sacrificial agent under Ultraviolet-Visible (UV-vis) light in N-2 and air ambient. (C) 2020 Elsevier Inc. All rights reserved.
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页码:20 / 29
页数:10
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