以金属有机骨架为牺牲模板制备MnOx-CeO2及其催化氧化

引用本文: 林雪婷, 付名利, 贺辉, 吴军良, 陈礼敏, 叶代启, 胡芸, 王逸凡, WENWilliam. 以金属有机骨架为牺牲模板制备MnO_x-CeO₂及其催化氧化[J]. 物理化学学报, 2018, 34(6): 719-730. doi: 10.3866/PKU.WHXB201712011 shu

Citation: LIN Xueting, FU Mingli, HE Hui, WU Junliang, CHEN Limin, YE Daiqi, HU Yun, WANG Yifan, WEN William. Synthesis of MnO_x-CeO₂ Using Metal-Organic Framework as Sacrificial Template and Its Performance in the Toluene Catalytic Oxidation Reaction[J]. Acta Physico-Chimica Sinica, 2018, 34(6): 719-730. doi: 10.3866/PKU.WHXB201712011 shu

以金属有机骨架为牺牲模板制备MnO_x-CeO₂及其催化氧化

1.
华南理工大学，环境与能源学院，广州 510006
2.
广东省大气环境与污染控制重点实验室，广州 510006
3.
挥发性有机物污染治理技术与装备国家工程实验室，广州 510006
4.
Centre for Clean Environment and Energy, Environmental Futures Centre, School of Environment, Griffith University, Gold Coast, QLD4222, Australia

通讯作者: 付名利, mlfu@scut.edu.cn

基金项目:

国家自然科学基金(No.51578245, No.51378213, No.51108187, No.21777047)，广东省自然科学基金项目(Grant No. 2016A030311003)

摘要: 以均苯三甲酸合铈-金属有机骨架(CeBTC-MOF)作为模板制备系列不同Mn含量的MnO_x-CeO₂催化剂，用于甲苯催化氧化。应用X射线衍射(XRD)、N₂物理吸附-脱附、热重分析(TG)、元素分析(EA)、电感耦合等离子体发射光谱法(ICP-OES)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、程序升温还原(H₂-TPR)、X射线光电子能谱(XPS)、拉曼光谱(Raman)和紫外可见漫反射(UV-vis)等手段对催化剂进行了表征。结果表明，通过MOF模板法制备的复合氧化物具备棒状形貌、高度分散、高比表面积和纳米晶体颗粒等特征。Mn在引入MOF的过程中，一部分进入CeO₂晶格形成固溶体，另一部分则分散在CeO₂表面，且分散的Mn分为单层分散态和晶相态。其中，CeO₂载体表面和Mn分散物之间的强相互作用是影响活性的重要因素。当表面分散的Mn低于单层分散阈值6.2%时，Mn以嵌入模型的形式与表面CeO₂发生强相互作用，有效促进催化剂的还原从而提高活性；当表面分散的Mn超过单层分散阈值6.2%时，载体表面形成Mn₃O₄晶相结构，对活性无明显促进作用。

关键词:

English

Synthesis of MnO_x-CeO₂ Using Metal-Organic Framework as Sacrificial Template and Its Performance in the Toluene Catalytic Oxidation Reaction

1.
School of Environment and Energy, South China University of Technology, Guangzhou 510006, P. R. China
2.
Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control (SCUT), Guangzhou 510006, P. R.China
3.
National Engineering Laboratory for VOCs Pollution Control Technology and Equipment, Guangzhou 510006, P. R. China
4.
Centre for Clean Environment and Energy, Environmental Futures Centre, School of Environment, Griffith University, Gold Coast, QLD4222, Australia

Corresponding author: FU Mingli, Email: mlfu@scut.edu.cn; Tel.: +86-13632349413

Received Date: 27 October 2017
Accepted Date: 27 November 2017
Revised Date: 20 November 2017
Available Online: 15 June 2018
Fund Project:

The project was supported by the National Natural Science Foundation of China (No.51578245, No.51378213, No.51108187, No.21777047), and the Guangdong Natural Science Foundation, China (Grant No. 2016A030311003)

Abstract: A series of MnO_x-CeO₂ with different Mn contents was prepared using CeBTC-MOF as the sacrificial template. These constituted a new kind of porous crystalline materials assembled by cerium as metal ions and 1, 3, 5-benzenetricarboxylic acid as organic ligands. The composite oxides exhibited good redox properties and were tested as catalysts in the oxidation of toluene. To obtain insight into the structure-activity relationship of the catalysts, the samples were characterized using powder X-ray diffraction (XRD), nitrogen adsorption-desorption, thermogravimetric analysis (TG), elemental analysis (EA), inductively coupled plasma-optical emission spectrometry (ICP-OES), scanning electron microscopy (SEM), transmission electron microscopy (TEM), H₂ temperature-programmed reduction (H₂-TPR), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy (Raman), and UV-Vis diffuse reflectance spectroscopy. Studies of the CeBTC-MOF template showed that the metal-organic framework could be completely decomposed at a calcination temperature of 300 ℃. Therefore, CeBTC-MOF decomposed and generated CO₂ and H₂O during the calcination process. The gas molecule spilled out from the structure to form the interior void space. The spilling out could be controlled by varying the calcination temperature. This regulated the quantity and size of the interior void, which in turn made the surface area controllable. The secondary building unit of CeBTC-MOF was oxidized to nano-sized crystalline particles, which exhibited outstanding interfacial contact. SEM and TEM results showed that the composite oxides prepared by pyrolysis of the CeBTC-MOF template exhibited rod-shaped nanocrystalline particles. While introducing Mn into MOF, part of Mn entered the ceria lattice to form solid solution and the remaining Mn was dispersed on CeO₂ surface. The elemental mappings revealed a well-proportioned distribution of Mn, which confirmed the successful formation of bimetallic metal oxides using the MOF-template method. All the samples exhibited sizes and shapes similar to their parent MOFs. As for catalytic activity, all the composite oxides showed better performances than pure CeO₂ for catalytic oxidation of toluene. This could be attributed to higher concentration of oxygen vacancies, which was characterized by Raman spectroscopy. In addition, the XPS results indicated that Mn⁴⁺/(Mn²⁺+Mn³⁺), Ce⁴⁺/Ce³⁺, O_latt (lattice oxygen), and O_sur(surface oxygen) all participated in the redox process during catalytic oxidation of toluene, which helped elucidate the mechanism at a micro level.Interestingly, the catalytic activity did not improve further when the Mn content of the composite oxides reached 5%. This could be ascribed to two different states of the dispersed Mn: monolayer dispersion state and crystalline phase. The strong interaction between ceria oxides and dispersed Mn species played an important role in affecting catalytic activity. The results showed the presence of a monolayer dispersion threshold (6.2%), confirmed by XPS characterization, which was in accordance with all the characterization results; it was proved that this threshold had a significant impact on the catalytic activity. When the dispersed Mn content was lower than the monolayer dispersion threshold, Mn reacted with the surface CeO₂ in the form of an incorporation model, leading to charge transfer and higher concentration of oxygen vacancies, which in turn effectively promoted the catalytic performance. When the dispersed Mn content exceeded the monolayer dispersion threshold, Mn₃O₄ was formed on the CeO₂ surface; this disrupted the promotion of catalytic activity, which explains the same catalytic activity of all the samples (5% MnO_x-CeO₂, 8% MnO_x-CeO₂, and 10% MnO_x-CeO₂).This successful formation of bimetallic metal oxides using CeBTC-MOF template indicated that composite oxide synthesis was feasible using the MOF template method. To obtain high catalyst performance of these composite oxides, it was important to control the metal content at the level of the monolayer dispersion threshold.

Key words:

1. [1]
  Kim, K.; Ahn, H. Appl. Catal. B: Environ. 2009, 91, 308.doi: 10.1016/j.apcatb.2009.05.037
2. [2]
  Li, P.; He, C.; Cheng, J.; Ma, C.; Dou, B.; Hao, Z. Appl. Catal. B: Environ. 2011, 101, 570. doi: 10.1016/j.apcatb.2010.10.030
3. [3]
  Liotta, L. Appl. Catal. B: Environ. 2010, 100, 403. doi: 10.1016/j.apcatb.2010.08.023
4. [4]
  De Rivas, B.; Fonseca, R.; Sampedro, C.; Gutiérrez-Ortiz, J. Appl. Catal. B: Environ. 2009, 90, 545. doi: 10.1016/j.apcatb.2009.04.017
5. [5]
  Okal, J.; Zawadzki, M. Appl. Catal. B: Environ.2009, 89, 22. doi: 10.1016/j.apcatb.2008.11.024
6. [6]
  Wu, X.; Liu, S.; Weng, D.; Lin, F.; Ran, R. Hazard. Mater. 2011, 187, 283. doi: 10.1016/j.jhazmat.2011.01.010
7. [7]
  Tikhomirov, K.; Krocher, O.; Elsener, M.; Wokaun, A. Appl. Catal. B: Environ. 2006, 64, 72. doi: 10.1016/j.apcatb.2005.11.003
8. [8]
  Becerra, M.; Arias, N.; Giraldo, O.; Suarez, F.; Gomez, M.; Lopez, A. Appl. Catal. B: Environ. 2011, 102, 260. doi: 10.1016/j.apcatb.2010.12.006
9. [9]
  Santos, V.; Pereira, M.; Orfao, J.; Figueiredo, J. Appl. Catal. B: Environ. 2010, 99, 353. doi: 10.1016/j.apcatb.2010.07.007
10. [10]
  Bastos, S.; Orfao, J.; Freitas, M.; Pereira, M.; Figueiredo, J. Appl. Catal. B: Environ. 2009, 93, 30. doi: 10.1016/j.apcatb.2009.09.009
11. [11]
  Shan, W.; Ma, N.; Yang, J.; Dong, X.; Liu, C.; Wei, L. J. Nat. Gas Chem. 2010, 19, 86. doi: 10.1016/S1003-9953[09]60033-5
12. [12]
  Champness, N.; Schroder, M. Curr. Opin. Solid. St. M. 1998, 3, 419. doi: 10.1016/S1359-0286[98]80055-7
13. [13]
  Zhang, L.; Wu, H.; Madhavi, S.; Hng, H.; Lou, X. J. Am. Chem. Soc. 2012, 134, 17388. doi: 10.1021/ja307475c
14. [14]
  Fuertes, A.; Centeno, T. J. Mater. Chem. 2005, 15, 1079. doi: 10.1039/b416007j
15. [15]
  Das, R.; Pachfule, P.; Banerjee, R.; Poddar, P. Nanoscale 2012, 4, 591. doi: 10.1039/c1nr10944h
16. [16]
  Zhang, F.; Chen, C.; Xiao, W.; Xu, L.; Zhang, N. Catal. Commun. 2012, 26, 25. doi: 10.1016/j.catcom.2012.04.028
17. [17]
  徐力, 陈超, 王瑞, 罗家还, 刘云凌, 张宁.高等学校化学学报, 2013, 34, 1907. doi: 10.7503 /cjcu20130260Xu, L.; Chen, C.; Wang, R.; Luo, J.; Liu, Y.; Zhang, N. Chem. J. Chin. Univ. 2013, 34, 1907. doi: 10.7503/cjcu20130260
18. [18]
  Liu, K.; You, H.; Jia, G.; Zheng, Y.; Huang, Y.; Song, Y.; Yang, M.; Zhang, L.; Zhang, H. Cryst. Growth Des. 2010, 10, 790. doi: 10.1021/cg901170j
19. [19]
  戴越, 李珊珊, 汤常金, 姚小江, 齐蕾, 刘斌, 高飞, 董林.无机化学学报, 2012, 28, 1555. http://www.cqvip.com/QK/93659X/201208/42657836.htmlDai, Y.; Li, S.; Tang, C.; Yao, X.; Qi, L.; Liu, B.; Gao, F.; Dong, L. Chin. J. Inorg. Chem. 2012, 28, 1555. http://www.cqvip.com/QK/93659X/201208/42657836.html
20. [20]
  王春明, 赵壁英, 谢有畅.催化学报, 2003, 24, 475. doi: 10.3321/j.issn:0253-9837.2003.06.017Wang, C.; Zhao, B.; Xie, Y. Chin. J. Catal. 2003, 24, 475. doi: 10.3321/j.issn:0253-9837.2003.06.017
21. [21]
  Kaliaguine, S.; Van Neste, A.; Szabo, V.; Gallot, J.; Bassir, M.; Muzychuk, R. Appl. Catal. A: Gen. 2001, 209, 345. doi: 10.1016/S0926-860X[00]00779-1
22. [22]
  Wu, Z.; Li, M.; Howe, J.; Meyer, H.; Overbury, S. Langmuir 2010, 26, 16595. doi: 10.1021/la101723w
23. [23]
  Hungria, A.; Fernandez-Garcia, M.; Anderson, J.; Martinez-Arias, A. J. Catal. 2005, 235, 262. doi: 10.1016/j.jcat.2005.08.012
24. [24]
  邓存, 段连运, 徐献平, 谢有畅.天然气化工, 1992, 6, 6.Deng, C.; Duan, L.; Xu, X.; Xie, Y. Nat. Gas Chem. Ind. 1992, 6, 6.
25. [25]
  Taniguchi, T.; Watanabe, T.; Sugiyama, N.; Subramani, A.; Wagata, H.; Matsushita, N.; Yoshimura, M. J. Phys. Chem. C 2009, 46, 19789. doi: 10.1021/jp9049457
26. [26]
  刘英骏, 吴江平, 郭沁林, 桂琳琳, 唐有祺.催化学报, 1987, 8, 14. http://www.ixueshu.com/document/aca8ef7586d054f5318947a18e7f9386.htmlLiu, Y.; Wu, J.; Guo, Q.; Gui, L.; Tang, Y. Chin. J. Catal. 1987, 8, 14. http://www.ixueshu.com/document/aca8ef7586d054f5318947a18e7f9386.html
27. [27]
  桂琳琳, 刘英骏, 郭沁林, 黄惠忠, 唐有祺.中国科学, 1985, 6, 509. http://www.ixueshu.com/document/70e03324790d2225318947a18e7f9386.htmlGui, L.; Liu, Y.; Guo, Q.; Huang, H.; Tang, Y.Sci. China Chem. 1985, 6, 509. http://www.ixueshu.com/document/70e03324790d2225318947a18e7f9386.html
28. [28]
  Zhang, Y.; Zhang, L.; Deng, J.; Dai, H.; He, H. Inorg. Chem. 2009, 48, 2181. doi: 10.1021/ic802195j
29. [29]
  Li, Y.; Sun, Q.; Kong, M.; Shi, W.; Huang, J.; Tang, J.; Zhao, X.J. Phys. Chem. C 2011, 115, 14050. doi: 10.1021/jp202720g
30. [30]
  Kan, J.; Deng, L.; Li, B.; Huang, Q.; Zhu, S.; Shen, S.; Chen, Y. Appl. Catal. A: Gen. 2017, 530, 21. doi: 10.1016/j.apcata.2016.11.013
31. [31]
  Wan, H.; Li, D.; Dai, Y.; Hu, Y.; Liu, B.; Dong, L. J. Mol. Catal. A -Chem. 2010, 332, 32. doi: 10.1016/j.molcata.2010.08.016
32. [32]
  Di Monte, R.; KasPar, J.; Fornasiero, P.; Graziani, M.; Paze, C.; Gubitosa, G. Inorg. Chim. Acta 2002, 334, 318. doi: 10.1016/S0020-1693[02]00800-9
33. [33]
  Qi, G.; Yang, R. J. Phys. Chem. B 2004, 108, 40. doi: 10.1021/jp048431h
34. [34]
  Wang, X.; Kang, Q.; Li, D. Appl. Catal. B: Environ. 2009, 86, 166. doi: 10.1016/j.apcatb.2008.08.009
35. [35]
  Rico-Pérez, V.; Aneggi, E.; Bueno-López, A.; Trovarelli, A. Appl. Catal. B: Environ.2016, 197, 95. doi: 10.1016/j.apcatb.2016.02.051
36. [36]
  Liao, Y.; Fu, M.; Chen, L.; Wu, J.; Huang, B.; Ye, D. Catal. Today 2013, 216, 220. doi: 10.1016/j.cattod.2013.06.017
37. [37]
  Lin, X.; Li, S.; He, H.; Wu, Z.; Wu, J.; Chen, L.; Ye, D.; Fu, M. Appl. Catal. B: Environ. 2017, doi: 10.1016/j.apcatb.2017.06.071
38. [38]
  刘小青, 李时卉, 孙梦婷, 喻成龙, 黄碧纯.物理化学学报, 2016, 32, 1236. doi: 10.3866/PKU.WHXB201602251Liu, X.; Li, S.; Sun, M.; Yu, C.; Huang, B. Acta Phys. -Chim. Sin. 2016, 32, 1236. doi: 10.3866/PKU.WHXB201602251
39. [39]
  Li, D.; Yu, Q.; Li, S.; Wan, H.; Liu, L.; Qi, L.; Liu, B.; Gao, F.; Dong, L.; Chen, Y. Chem.-A Eur. J. 2011, 17, 5668. doi: 10.1002/chem.201002786
40. [40]
  张玉芬, 谢有畅, 张阳, 张德龙, 唐有祺.中国科学, 1986, 8, 805. http://chem.scichina.com:8081/sciB//CN/abstract/abstract395009.shtmlZhang, Y.; Xie, Y.; Zhang, Y.; Zhang, D.; Tang, Y. Sci. China Chem. 1986, 8, 805. http://chem.scichina.com:8081/sciB//CN/abstract/abstract395009.shtml
41. [41]
  Parida, K.; Dash, S.; Singha, S. Appl. Catal. A: Gen. 2008, 351, 59. doi: 10.1016/j.apcata.2008.08.027
42. [42]
  郁青春, 张世超, 王新东.工业催化, 2007, 15, 12. http://www.cqvip.com/Main/Detail.aspx?id=24037731Yu, Q.; Zhang, S.; Wang, X. Ind. Catal. 2007, 15, 12. http://www.cqvip.com/Main/Detail.aspx?id=24037731
43. [43]
  董林, 陈懿.无机化学学报, 2000, 2, 250. doi: 10.3321/j.issn:1001-4861.2000.02.011Dong, L.; Chen, Y. Chinese J. Inorg. Chem. 2000, 2, 250. doi: 10.3321/j.issn:1001-4861.2000.02.011

扫一扫看文章

计量

PDF下载量: 8
文章访问数: 525
HTML全文浏览量: 39

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

以金属有机骨架为牺牲模板制备MnO_x-CeO₂及其催化氧化

通讯作者: 付名利, mlfu@scut.edu.cn

English

Synthesis of MnO_x-CeO₂ Using Metal-Organic Framework as Sacrificial Template and Its Performance in the Toluene Catalytic Oxidation Reaction

Corresponding author: FU Mingli, Email: mlfu@scut.edu.cn; Tel.: +86-13632349413

CCS Chemistry：嵌段共聚物自组装成 “三明治”二维有机材料，实现纳米级压力传感功能

CCS Chemistry：颜徐州、鲍哲南：你的皮肤可能是一片SPMs

CCS Chemistry：工作高效不疲劳，只须让催化剂动起来

CCS Chemistry：静电组装导向聚合- 聚电解质纳米凝胶量化制备新策略

CCS Chemistry：金黄色葡萄球菌醛基脱氢酶是如何识别特异性底物的？

计量

通讯作者: 陈斌, bchen63@163.com

中国化学会秘书处