机构:
Tianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R ChinaTianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R China
Zeng, Lirong
[1
]
Cui, Lan
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机构:
Tianjin Univ, Ctr Anal, Tianjin 300072, Peoples R ChinaTianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R China
Cui, Lan
[2
]
Wang, Caiyun
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机构:
Tianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R ChinaTianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R China
Wang, Caiyun
[1
]
Guo, Wei
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机构:
Tianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R ChinaTianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R China
Guo, Wei
[1
]
Gong, Cairong
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Tianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R ChinaTianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R China
Gong, Cairong
[1
]
机构:
[1] Tianjin Univ, Sch Mat Sci & Engn, Inst New Energy, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Ctr Anal, Tianjin 300072, Peoples R China
In this work, the Ag loaded Ce-based catalyst was synthesized (by the sol-gel method) and its performance was studied by TG, H-2-TPR, XRD, SEM, TEM, BET and XPS. The results show that Ag nanoparticles be successfully loaded onto the CeO2 surface and the relative content of Ag nanoparticles is about 10.22 wt.% close to the theoretical value (10%). XPS shows that Ag nanoparticles induce a great number of oxygen vacancies in the CeO2 lattice through the electronic transfer, and H-2-TPR indicates that the Ag-assisted CeO2 catalyst exhibits a better reduction performance and Ag nanoparticles can promote O- transform into O2-. The catalytic activity for soot oxidation was studied by TG under air atmosphere and the activity was found to be obviously enhanced when Ag nanoparticles be load on the surface of CeO2 (T-10 = 386 degrees C, T-90 = 472.5 degrees C, T-m = 431 degrees C). The reaction mechanism was also presented and O-2(-) species is regarded as the determinant factor for the catalytic activity.
机构:
Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, IndiaIndian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Bera, P
Patil, KC
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机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Patil, KC
Hegde, MS
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机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
机构:
Tsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R ChinaTsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
Weng, Duan
Li, Jia
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机构:
Tsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R ChinaTsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
Li, Jia
Wu, Xiaodong
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机构:
Tsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R ChinaTsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
Wu, Xiaodong
Si, Zhichun
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机构:
Tsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R ChinaTsinghua Univ, Dept Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R China
机构:
Beijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R ChinaBeijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R China
Huang, Junfeng
Wang, Shanshan
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机构:
Beijing Inst Technol, Anal & Testing Ctr, Beijing 10081, Peoples R ChinaBeijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R China
Wang, Shanshan
Wang, Xiaochen
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机构:
Changan Univ, Shaanxi Key Lab New Transportat Energy & Automot E, Xian 710064, Peoples R ChinaBeijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R China
Wang, Xiaochen
Gao, Jianbing
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机构:
Beijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R ChinaBeijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R China
Gao, Jianbing
Wang, Yufeng
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机构:
Beijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R ChinaBeijing Inst Technol, Sch Mech Engn, Beijing 10081, Peoples R China
机构:
Tsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R ChinaTsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R China
Zheng, Changlong
Wu, Xiaodong
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机构:
Tsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R ChinaTsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R China
Wu, Xiaodong
Li, Zhenguo
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h-index: 0
机构:
China Automot Technol & Res Ctr, Natl Engn Lab Mobile Source Emiss Control Technol, Tianjin 300300, Peoples R ChinaTsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R China
Li, Zhenguo
Ran, Rui
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机构:
Tsinghua Univ, Sch Mat Sci & Engn, State Key Lab New Ceram & Fine Proc, Beijing 100084, Peoples R ChinaTsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R China
Ran, Rui
Weng, Duan
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机构:
Tsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R ChinaTsinghua Univ, Sch Mat Sci & Engn, Key Lab Adv Mat, Minist Educ, Beijing 100084, Peoples R China
机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Sarode, PR
Priolkar, KR
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机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Priolkar, KR
Bera, P
论文数: 0引用数: 0
h-index: 0
机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Bera, P
Hegde, MS
论文数: 0引用数: 0
h-index: 0
机构:
Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, IndiaIndian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Hegde, MS
Emura, S
论文数: 0引用数: 0
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机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
Emura, S
Kumashiro, R
论文数: 0引用数: 0
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机构:Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India