Z型Ag3PO4/Ag2MoO4异质结光催化剂构建和光催化降解有机污染物

doi:10.1016/S1872-2067(16)62570-6

催化学报 ›› 2017, Vol. 38 ›› Issue (2): 337-347.DOI: 10.1016/S1872-2067(16)62570-6

Z型Ag₃PO₄/Ag₂MoO₄异质结光催化剂构建和光催化降解有机污染物

唐华^a, 付彦惠^a, 苌树方^a, 谢思雨^a, 唐国刚^a,b

a 江苏大学材料科学与工程学院, 江苏镇江 212003;
b 镇江高等专科学校化学与材料工程学院, 江苏镇江 212003

收稿日期:2016-08-28 修回日期:2016-09-30 出版日期:2017-02-18 发布日期:2017-03-14
通讯作者: Hua Tang,Tel/Fax:+86-511-88790268;E-mail:tanghua@mail.ujs.edu.cn
基金资助:
国家自然科学基金（51672113，51302112）；武汉理工大学复合新技术国家重点实验室开放基金（2016-KF-10）.

Construction of Ag₃PO₄/Ag₂MoO₄ Z-scheme heterogeneous photocatalyst for the remediation of organic pollutants

Hua Tang^a, Yanhui Fu^a, Shufang Chang^a, Siyu Xie^a, Guogang Tang^a,b

a School of Materials Science and Engineering, Jiangsu University, Zhenjiang 212013, Jiangsu, China;
b School of Chemistry and Materials Engineering, Zhenjiang College, Zhenjiang 212003, Jiangsu, China

Received:2016-08-28 Revised:2016-09-30 Online:2017-02-18 Published:2017-03-14
Contact: 10.1016/S1872-2067(16)62570-6
Supported by:
This work was supported by the National Natural Science Foundation of China (51672113, 51302112) and the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing (Wuhan University of Technology, 2016-KF-10).

摘要/Abstract

摘要：

作为一种绿色技术，半导体光催化氧化广泛应用于环境污染物治理和太阳能转化领域.高效、稳定、可回收利用催化剂的开发是光催化技术发展的一个重要方向.Ag系半导体光催化剂因在可见光分解水制氢及降解有机污染物等方面表现出优异的催化性能而广受关注.然而，该催化剂失活快，制约了其应用.因此，提高Ag系半导体材料的光催化稳定性成为近年研究热点.在各种Ag基光催化剂中，Ag₃PO₄光催化剂因其在可见光下光氧化水产生O₂以及有机染料的光催化分解中有着高的量子效率，引起了人们广泛关注.如何进一步提升Ag₃PO₄光催化剂性能及在光催化过程中的稳定性成为研究焦点，包括Ag₃PO₄光催化剂的特殊形貌和晶体结构控制生长以及复合材料控制制备.但是Z型Ag₃PO₄基可见光催化剂的构筑仍然是一个挑战.
本文利用Ag₂MoO₄和Ag₃PO₄的溶液相反应法合成了Z型Ag₃PO₄/Ag₂MoO₄复合光催化剂，通过Ag₃PO₄/Ag₂MoO₄异质结光催化剂在可见光下降解罗丹明B（RhB）、亚甲基橙（MO）、亚甲基蓝（MB）和苯酚研究了其光催化性能，采用X射线衍射（XRD）、能谱、傅立叶变换红外光谱（FT-IR）、拉曼光谱、场发射扫描电子显微镜（FE-SEM）以及紫外可见漫反射光谱（UV-vis）等手段表征了该催化剂.
XRD，FTIR和拉曼光谱结果表明，复合材料由Ag₃PO₄，Ag₂MoO₄和单质银组成，表面成功合成了Z构型Ag₃PO₄/Ag/Ag₂MoO₄复合材料.SEM结果发现纯Ag₃PO₄是规则的球状，纯Ag₂MoO₄则是多面体状块的颗粒，在Ag₃PO₄/Ag₂MoO₄复合材料中可以看到规则的球状体Ag₃PO₄和Ag₂MoO₄纳米颗粒，并且随着Ag₂MoO₄含量的增加，Ag₃PO₄颗粒的尺寸逐渐减小.UV-vis结果发现Ag₂MoO₄的加入拓展了复合材料对可见光的吸收范围.光催化性能测试结果表明，8% Ag₂MoO₄/Ag₃PO₄在可见光下具有优异的光催化性能：可见光照射5 min，RhB，MO和MB的降解效率分别可达95%，97%和90%.复合材料样品经过4个循环实验后，其降解RhB的效率仍然保持在84%，证明了其具有较高的稳定性.
为了进一步研究Ag₃PO₄/Ag₂MoO₄的光催化机理，我们用对苯醌、乙二胺四乙酸二钠和丁醇进行了捕捉剂实验.结果表明，超氧自由基和光生空穴在降解有机染料过程中起主要作用.通过光电流测试、复合材料价带导带位置计算以及循环过程样品XRD分析并结合文献结果认为，Z构型Ag₃PO₄/Ag/Ag₂MoO₄异质结光催化体系以及可见光照射初期金属Ag纳米颗粒的生成是其具有高光催化活性和稳定性的原因.

关键词: Z型异质结, 磷酸银, 杂化材料, 电荷转移, 光催化

Abstract:

Hole/electron separation and charge transfer are the key processes for enhancing the visible-light photocatalysis performance of heterogeneous photocatalytic systems. To better utilize and understand these effects, binary Ag₃PO₄/Ag₂MoO₄ hybrid materials were fabricated by a facile solution-phase reaction and characterized systematically by X-ray diffraction (XRD), energy-dispersive spectroscopy, Fourier transform infrared spectroscopy, Raman spectroscopy, field-emission scanning electron microscopy and ultraviolet-visible diffuse-reflectance spectroscopy. Under visible-light illumination, a heterogeneous Ag₃PO₄/Ag/Ag₂MoO₄ photocatalyst was constructed and demonstrated enhanced photocatalytic activity and photostability compared with pristine Ag₃PO₄ toward the remediation of the organic dye rhodamine B. The Ag₃PO₄/Ag₂MoO₄ hybrid catalyst with 8% mole fraction of Ag₂MoO₄ exhibited the highest photocatalytic activity toward the removal of typical dye molecules, including methyl orange, methylene blue and phenol aqueous solution. Moreover, the mechanism of the photocatalytic enhancement was investigated via hole- and radical-trapping experiments, photocurrent measurements, electrochemical impedance spectroscopy and XRD measurements. The XRD analysis revealed that metallic Ag nanoparticles formed initially on the surface of the Ag₃PO₄/Ag₂MoO₄ composites under visible-light illumination, leading to the generation of a Ag₃PO₄/Ag/Ag₂MoO₄ Z-scheme tandem photocatalytic system. The enhanced photocatalytic activity and stability were attributed to the formation of the Ag₃PO₄/Ag/Ag₂MoO₄ Z-scheme heterojunction and surface plasmon resonance of photo-reduced Ag nanoparticles on the surface. Finally, a plasmonic Z-scheme photocatalytic mechanism was proposed. This work may provide new insights into the design and preparation of advanced visible-light photocatalytic materials and facilitate their practical application in environmental issues.

Key words: Z-scheme heterojunction, Silver phosphate, Hybrid material, Charge transfer, Photocatalysis

唐华, 付彦惠, 苌树方, 谢思雨, 唐国刚. Z型Ag₃PO₄/Ag₂MoO₄异质结光催化剂构建和光催化降解有机污染物[J]. 催化学报, 2017, 38(2): 337-347.

Hua Tang, Yanhui Fu, Shufang Chang, Siyu Xie, Guogang Tang. Construction of Ag₃PO₄/Ag₂MoO₄ Z-scheme heterogeneous photocatalyst for the remediation of organic pollutants[J]. Chinese Journal of Catalysis, 2017, 38(2): 337-347.

×
扫码分享

导出引用管理器 EndNote|Ris|BibTeX

链接本文: https://www.cjcatal.com/CN/10.1016/S1872-2067(16)62570-6

https://www.cjcatal.com/CN/Y2017/V38/I2/337

参考文献

[1] S. W. Cao, J. X. Low, J. G. Yu, M. Jaroniec, Adv. Mater., 2015, 27, 2150-2176.
[2] M. Marszewski, S. W. Cao, J. G. Yu, M. Jaroniec, Mater. Horiz., 2015, 2, 261-278.
[3] Q. J. Xiang, B. Cheng, J. G. Yu, Angew. Chem. Int. Ed., 2015, 54, 11350-11366.
[4] Q. Li, X. Li, S. Wageh, A. A. Al-Ghamdi, J. G. Yu, Adv. Energy Mater., 2015, 5, 1500010.
[5] X. Li, J. G. Yu, M. Jaroniec, Chem. Soc. Rev., 2016, 45, 2603-2636.
[6] K. F. Wu, T. Q. Lian, Chem. Soc. Rev., 2016, 45, 3781-3810.
[7] L. K. Putri, W. J. Ong, W. S. Chang, S. P. Chai, Appl. Surf. Sci., 2015, 358, 2-14.
[8] S. Ye, R. Wang, M. Z. Wu, Y. P. Yuan, Appl. Surf. Sci., 2015, 358, 15-27.
[9] W. J. Ong, L. L. Tan, Y. H. Ng, S. T. Yong, S. P. Chai, Chem. Rev., 2016, 116, 7159-7329.
[10] J. Schneider, M. Matsuoka, M. Takeuchi, J. Zhang, Y. Horiuchi, M. Anpo, D. W. Bahnemann, Chem. Rev., 2014, 114, 9919-9986.
[11] H. Tang, D. Zhang, G. G. Tang, X. R. Ji, C. S. Li, X. H. Yan, K. Q. Wu, J. Alloy. Compd., 2014, 591, 52-57.
[12] M. Pelaez, N. T. Nolan, S. C. Pillai, M. K. Seery, P. Falaras, A. G. Kontos, P. S. M. Dunlop, J. W. J. Hamilton, J. A. Byrne, K. O'shea, M. H. Entezari, D. D. Dionysiou, Appl. Catal. B, 2012, 125, 331-349.
[13] X. F. Wang, R. Yu, K. Wang, G. Q. Yang, H. G. Yu, Chin. J. Catal., 2015, 36, 1211-2218.
[14] J. Q. Wen, X. Li, W. Liu, Y. P. Fang, J. Xie, Y. H. Xu, Chin. J. Catal., 2015, 36, 2049-2070.
[15] M. C. Wen, S. S. Zhang, W. R. Dai, G. S. Li, D. Q. Zhang, Chin. J. Catal., 2015, 36, 2095-2102.
[16] J. L. Xie, Y. F. Yang, H. P. He, D. Cheng, M. M. Mao, Q. X. Jiang, L. X. Song, J. Xiong, Appl. Surf. Sci., 2015, 355, 921-929.
[17] J. G. Yu, S. H. Wang, J. X. Low, W. Xiao, Phys. Chem. Chem. Phys., 2013, 15, 16883-16890.
[18] H. Tang, S. F. Chang, K. Q. Wu, G. G. Tang, Y. H. Fu, Q. Q. Liu, X. F. Yang, RSC Adv., 2016, 6, 63117-63130.
[19] H. L. Wang, L. S. Zhang, Z. G. Chen, J. Q. Hu, S. J. Li, Z. H. Wang, J. S. Liu, X. C. Wang, Chem. Soc. Rev., 2014, 43, 5234-5244.
[20] H. Tong, S. X. Ouyang, Y. P. Bi, N. Umezawa, M. Oshikiri, J. H. Ye, Adv. Mater., 2012, 24, 229-251.
[21] J. D. Li, W. Fang, C. L. Yu, W. Q. Zhou, L. H. Zhu, Y. Xie, Appl. Surf. Sci., 2015, 358, 46-56.
[22] Z. F. Zhao, Y. Z. Wang, J. Xu, C. Y. Shang, Y. Wang, Appl. Surf. Sci., 2015, 351, 416-424.
[23] D. Zhang, H. Tang, Y. Q. Wang, K. Q. Wu, H. Huang, G. G. Tang, J. Yang, Appl. Surf. Sci., 2014, 319, 306-311.
[24] M. Cui, J. X. Yu, H. J. Lin, Y. Wu, L. H. Zhao, Y. M. He, Appl. Surf. Sci., 2016, 387, 912-920.
[25] X. F. Wang, S. F. Li, H. G. Yu, J. G. Yu, S. W. Liu, Chem-Eur. J., 2011, 17, 7777-7780.
[26] H. Tang, S. F. Chang, G. G. Tang, W. Liang, Appl. Surf. Sci., 2016, doi:10.1016/j.apsusc.2016.07.021.
[27] B. C. Zhu, P. F. Xia, Y. Li, W. Ho, J. G. Yu, Appl. Surf. Sci., 2016, doi:10.1016/j.apsusc.2016.07.104.
[28] J. Andrés, M. M. Ferrer, L. Gracia, A. Beltran, V. M. Longo, G. H. Cruvinel, R. L. Tranquilin, E. Longo, Part. Part. Syst. Char., 2015, 32, 646-651.
[29] D. F. Xu, B. Cheng, J. F. Zhang, W. K. Wang, J. G. Yu, W. Ho, J. Mater. Chem. A, 2015, 3, 20153-20166.
[30] Z. Z. Lou, B. B. Huang, Z. Y. Wang, X. Y. Ma, R. Zhang, X. Y. Zhang, X. Y. Qin, Y. Dai, M. H. Whangbo, Chem. Mater., 2014, 26, 3873-3875.
[31] Z. G. Yi, J. H. Ye, N. Kikugawa, T. Kako, S. Ouyang, H. Stu-art-Williams, H. Yang, J. Y. Cao, W. J. Luo, Z. S. Li, Y. Liu, R. L. With-ers, Nat. Mater., 2010, 9, 559-564.
[32] X. F. Yang, H. Tang, J. S. Xu, M. Antonietti, M. Shalom, ChemSus-Chem, 2015, 8, 1350-1358.
[33] H. C. Wang, Z. F. Ye, C. Liu, J. Z. Li, M. J. Zhou, Q. F. Guan, P. Lv, P. W. Huo, Y. S. Yan, Appl. Surf. Sci., 2015, 353, 391-399.
[34] L. Cai, X. L. Xiong, N. G. Liang, Q. Y. Long, Appl. Surf. Sci., 2015, 353, 939-948.
[35] P. Y. Dong, Y. H. Wang, H. H. Li, H. Li, X. L. Ma, L. L. Han, J. Mater. Chem. A, 2013, 1, 4651-4656.
[36] C. T. Dinh, T. D. Nguyen, F. Kleitz, T. O. Do, Chem. Commun., 2011, 47, 7797-7799.
[37] Y. P. Bi, S. X. Ouyang, N. Umezawa, J. Y. Cao, J. H. Ye, J. Am. Chem. Soc., 2011, 133, 6490-6492.
[38] Z. H. Chen, W. L. Wang, Z. G. Zhang, X. M. Fang, J. Phys. Chem. C, 2013, 117, 19346-19352.
[39] X. Wang, M. Utsumi, Y. G. Yang, D. W. Li, Y. X. Zhao, Z. Y. Zhang, C. P. Feng, N. Sugiura, J. J. Cheng, Appl. Surf. Sci., 2015, 325, 1-12.
[40] H. L. Lin, H. F. Ye, B. Y. Xu, J. Cao, S. F. Chen, Catal. Commun., 2013, 37, 55-59.
[41] C. S. Zhu, L. Zhang, B. Jiang, J. T. Zheng, P. Hu, S. J. Li, M. B. Wu, W. T. Wu, Appl. Surf. Sci., 2016, 377, 99-108.
[42] Z. H. Chen, F. Bing, Q. Liu, Z. G. Zhang, X. M. Fang, J. Mater. Chem. A, 2015, 3, 4652-4658.
[43] P. Zhou, J. G. Yu, M. Jaroniec, Adv. Mater., 2014, 26, 4920-4935.
[44] D. F. Xu, B. Cheng, S. W. Cao, J. G. Yu, Appl. Catal. B, 2015, 164, 380-388.
[45] W. Chen, T. Liu, T. Y. Huang, X. H. Liu, J. W. Zhu, G. R. Duan, X. J. Yang, Appl. Surf. Sci., 2015, 355, 379-387.
[46] J. Q. Li, H. Yuan, Z. F. Zhu, Appl. Surf. Sci., 2016, 385, 34-41.
[47] Y. Y. Bai, Y. Lu, J. K. Liu, J. Hazard. Mater., 2016, 307, 26-35.
[48] B. Chai, J. Li, Q. Xu, Ind. Eng. Chem. Res., 2014, 53, 8744-8752.
[49] A. F. Gouveia, J. C. Sczancoski, M. M. Ferrer, A. S. Lima, M. R. M. C. Santos, M. S. Li, R. S. Santos, E. Longo, L. S. Cavalcante, Inorg. Chem., 2014, 53, 5589-5599.
[50] Z. Li, X. T. Chen, Z. L. Xue, Sci. China Chem., 2013, 56, 443-450.
[51] J. Cao, B. D. Luo, H. L. Lin, B. Y. Xu, S. F. Chen, J. Hazard. Mater., 2012, 217, 107-115.
[52] H. J. Dong, G. Chen, J. X. Sun, Y. J. Feng, C. M. Li, G. H. Xiong, C. D. Lv, Dalton Trans., 2014, 43, 7282-7289.
[53] Z. Y. Zhang, D. L. Jiang, C. S. Xing, L. L. Chen, M. Chen, M. Q. He, Dal-ton Trans., 2015, 44, 11582-11591.
[54] H. Zangeneh, A. A. L. Zinatizadeh, M. Habibi, M. Akia, M. Hasnain Isa, J. Ind. Eng. Chem., 2015, 26, 1-36.
[55] K. F. Wu, H. M. Zhu, Z. Liu, W. Rodríguez-Córdoba, T. Q. Lian, J. Am. Chem. Soc., 2012, 134, 10337-10340.
[56] J. G. Yu, T. T. Ma, S. W. Liu, Phys. Chem. Chem. Phys., 2011, 13, 3491-3501.
[57] K. F. Wu, Z. Y. Chen, H. J. Lv, H. M. Zhu, C. L. Hill, T. Q. Lian, J. Am. Chem. Soc., 2014, 136, 7708-7716.
[58] X. F. Yang, J. L. Qin, Y. Jiang, K. M. Chen, X. H. Yan, D. Zhang, R. Li, H. Tang, Appl. Catal. B, 2015, 166, 231-240.
[59] H. Y. Li, Y. J. Sun, B. Cai, S. Y. Gan, D. X. Han, L. Niu, T. S. Wu, Appl. Catal. B, 2015, 170, 206-214.
[60] J. G. Hou, Z. Wang, C. Yang, W. L. Zhou, S. Q. Jiao, H. M. Zhu, J. Phys. Chem. C, 2013, 117, 5132-5141.
[61] H. J. Cheng, J. G. Hou, H. M. Zhu, X. M. Guo, RSC Adv., 2014, 4, 41622-41630.
[62] X. F. Wang, S. F. Li, Y. Q. Ma, H. G. Yu, J. G. Yu, J. Phys. Chem. C, 2011, 115, 14648-14655.

Z型Ag₃PO₄/Ag₂MoO₄异质结光催化剂构建和光催化降解有机污染物

Construction of Ag₃PO₄/Ag₂MoO₄ Z-scheme heterogeneous photocatalyst for the remediation of organic pollutants

PDF

可视化

摘要/Abstract

引用本文

使用本文

扫码分享

参考文献

相关文章 15

编辑推荐

Metrics

[1]	赵彬彬, 钟威, 陈峰, 王苹, 别传彪, 余火根. 高晶化g-C₃N₄光催化剂: 合成、结构调控和光催化产氢[J]. 催化学报, 2023, 52(9): 127-143.
[2]	唐小龙, 李锋, 李方, 江燕斌, 余长林. 单原子催化剂在光催化和电催化合成过氧化氢中的研究进展[J]. 催化学报, 2023, 52(9): 79-98.
[3]	蔡铭洁, 刘艳萍, 董珂欣, 陈晓波, 李世杰. 漂浮型Bi₂WO₆/C₃N₄/碳布S型异质结光催化材料用于高效净化水体环境[J]. 催化学报, 2023, 52(9): 239-251.
[4]	王思恺, 闵祥婷, 乔波涛, 颜宁, 张涛. 单原子催化: 追寻催化领域的“圣杯”[J]. 催化学报, 2023, 52(9): 1-13.
[5]	江梓聪, 程蓓, 张留洋, 张振翼, 别传彪. 氧化锌基梯型异质结光催化剂[J]. 催化学报, 2023, 52(9): 32-49.
[6]	刘博文, 蔡家杰, 张建军, 谭海燕, 程蓓, 许景三. MOF/CdS梯型光催化剂同时进行苯甲醇氧化和析氢反应及其机理研究[J]. 催化学报, 2023, 51(8): 204-215.
[7]	宋明明, 宋相海, 刘鑫, 周伟强, 霍鹏伟. ZnIn₂S₄/MOF-808微球结构S型异质结光催化剂的制备及其光还原CO₂性能研究[J]. 催化学报, 2023, 51(8): 180-192.
[8]	邵秀丽, 李可, 李静萍, 程强, 王国宏, 王楷. 揭示NiS@Ta₂O₅纳米纤维中梯型电荷转移路径及光催化CO₂转化性能[J]. 催化学报, 2023, 51(8): 193-203.
[9]	李嘉明, 李源, 王小田, 杨直雄, 张高科. TiO₂上原子分散的Fe位点促进光催化CO₂还原: 增强的催化活性、 DFT计算和机制洞察[J]. 催化学报, 2023, 51(8): 145-156.
[10]	阎菲, 张由子, 刘思碧, 邹睿卿, Jahan B Ghasemi, 李炫华. 供体-受体型卟啉基金属有机框架实现有效电荷分离高效光催化析氢[J]. 催化学报, 2023, 51(8): 124-134.
[11]	孙利娟, 王伟康, 路平, 刘芹芹, 王乐乐, 唐华. 纳米高熵合金实现光催化剂肖特基势垒的调控用于光催化制氢与苯甲醇氧化耦合反应[J]. 催化学报, 2023, 51(8): 90-100.
[12]	刘海峰, 黄祥, 陈加藏. 电子态调控促进氢气无损耗纯化中CO的光致富集和氧化[J]. 催化学报, 2023, 51(8): 49-54.
[13]	袁鑫, 范海滨, 刘杰, 覃龙州, 王剑, 段秀, 邱江凯, 郭凯. 连续流技术在光氧化还原催化转化的最新进展[J]. 催化学报, 2023, 50(7): 175-194.
[14]	余治晗, 关晨, 岳晓阳, 向全军. 碳环渗入的结晶氮化碳S型同质结及其光催化析氢[J]. 催化学报, 2023, 50(7): 361-371.
[15]	李慧杰, 池漫洲, 辛兴, 王瑞杰, 刘天府, 吕红金, 杨国昱. 异金属取代的多金属氧酸盐@光响应型金属-有机框架用于高选择性光催化CO₂还原[J]. 催化学报, 2023, 50(7): 343-351.