Tuning the N-bonded cerium(iii) fraction/g-C3N4 interface in hollow structures using an in situ reduction treatment for superior photochemical hydrogen evolution Electronic supplementary information (ESI) available. See DOI: 10.1039/c9cy01305a

CORC > 生态环境研究中心 > 中国科学院生态环境研究中心 > 中国科学院饮用水科学与技术重点实验室

	Tuning the N-bonded cerium(iii) fraction/g-C3N4 interface in hollow structures using an in situ reduction treatment for superior photochemical hydrogen evolution Electronic supplementary information (ESI) available. See DOI: 10.1039/c9cy01305a
	Waqas, Muhammad ; Yang, Bo ; Cao, Lujie ; Zhao, Xu ; Iqbal, Waheed ; Xiao, Ke ; Zhu, Caizhen ; Zhang, Junmin
刊名	CATALYSIS SCIENCE & TECHNOLOGY
	2019-10-07
卷号	9 期号:19 页码:5322-5332
ISSN号	2044-4753
英文摘要	The synthesis of inorganic/organic interfaces in spherical hollow structures (HS) is a promising but challenging task. Herein, we innovatively utilized porous CeO2-HS as a scaffold to incorporate cyanamide molecules, which upon one-step in situ reducing treatment, yielded nitrogen-bonded CeO2-x/g-C3N4-HS. The electron microscope and spectroscopic analysis validated two functions of cyanamide: i) it generates an in situ reducing atmosphere (CO, N-2, NOx) to tune the cerium oxide vacancy population, and ii) it acts as a N and g-C3N4 precursor. Meanwhile, the unique HS geometry promotes cerium oxide reduction at low temperature due to the following: i) the high surface area of CeO2-HS provides a larger area for CeO2/CO interaction; ii) adequate pore volume enhances the cerium oxide reduction kinetics; and, iii) the CeO2 nanoparticles increase the ceria surface defect population by obeying the ceria oxygen vacancy transport model. Remarkably, the N-CeO2-x/g-C3N4-HS photocatalyst hydrogen evolution rate is 43.32 mu mol g(-1) h(-1) under visible light (lambda >= 420 nm), which is 3.8 times higher than pristine g-C3N4 (11.4 mu mol g(-1) h(-1)) due to: a) enhancement of the material's light-harvesting ability by HS, b) formation of controlled optically active Ce3+ sites, and c) intimate inorganic/organic interfaces, which boosted the minority carriers' separation efficiency.
内容类型	期刊论文
源URL	[http://ir.rcees.ac.cn/handle/311016/43545]
专题	生态环境研究中心_中国科学院饮用水科学与技术重点实验室
作者单位	1.Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Peoples R China 2.Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Key Lab Drinking Water Sci & Technol, Beijing 100085, Peoples R China 3.Shenzhen Univ, Coll Chem & Environm Engn, Shenzhen 518060, Peoples R China
推荐引用方式 GB/T 7714	Waqas, Muhammad,Yang, Bo,Cao, Lujie,et al. Tuning the N-bonded cerium(iii) fraction/g-C3N4 interface in hollow structures using an in situ reduction treatment for superior photochemical hydrogen evolution Electronic supplementary information (ESI) available. See DOI: 10.1039/c9cy01305a[J]. CATALYSIS SCIENCE & TECHNOLOGY,2019,9(19):5322-5332.
APA	Waqas, Muhammad.,Yang, Bo.,Cao, Lujie.,Zhao, Xu.,Iqbal, Waheed.,...&Zhang, Junmin.(2019).Tuning the N-bonded cerium(iii) fraction/g-C3N4 interface in hollow structures using an in situ reduction treatment for superior photochemical hydrogen evolution Electronic supplementary information (ESI) available. See DOI: 10.1039/c9cy01305a.CATALYSIS SCIENCE & TECHNOLOGY,9(19),5322-5332.
MLA	Waqas, Muhammad,et al."Tuning the N-bonded cerium(iii) fraction/g-C3N4 interface in hollow structures using an in situ reduction treatment for superior photochemical hydrogen evolution Electronic supplementary information (ESI) available. See DOI: 10.1039/c9cy01305a".CATALYSIS SCIENCE & TECHNOLOGY 9.19(2019):5322-5332.