Polyoxometalate immobilized in MIL-101(Cr) as an efficient catalyst for water oxidation

被引:74
|
作者
Han, Jianyu [1 ,2 ]
Wang, Danping [3 ]
Du, YongHua [4 ]
Xi, Shibo [4 ]
Chen, Zhong [3 ]
Yin, Shengming [1 ]
Zhou, Tianhua [1 ]
Xu, Rong [1 ,5 ]
机构
[1] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
[2] Nanyang Technol Univ, Energy Res Inst NTU, 50 Nanyang Dr, Singapore 637553, Singapore
[3] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[4] Inst Chem & Engn Sci, 1 Pesek Rd, Singapore 627833, Singapore
[5] Natl Res Fdn, CREATE C4T, CREATE Tower Level 11,1 Create Way, Singapore 138602, Singapore
基金
新加坡国家研究基金会;
关键词
Polyoxometalates; MIL-101; Water oxidation; Photocatalysis; Electrocatalysis; METAL-ORGANIC FRAMEWORK; OXYGEN-EVOLVING CATALYST; PHOSPHOTUNGSTIC ACID; CARBON; LIGHT; FUEL; ENCAPSULATION; CHEMISTRY; PHOSPHATE;
D O I
10.1016/j.apcata.2015.10.015
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
Water oxidation is an essential reaction in artificial photosynthesis. Finding efficient and stable catalysts for this reaction is still a challenging task. Recently, a series of polyoxometalates (POMs) comprised of earth abundant materials are reported to be efficient water oxidation catalysts (WOCs). In this study, we investigated the effect of a support material to the catalytic performance of [Co(H2O)2(PW9O34)(2)](10-) (CoPOM) by immobilizing this molecular POM-based catalyst on MIL-101(Cr), a highly porous and robust metal-organic framework (MOF). The successful encapsulation of CoPOM in MIL-101 achieved by a facile ion exchange method was evidenced by combined XRD, FTIR, XPS, XANES, TEM and elemental mapping analyses. Both the photocatalytic and electrochemical studies have indicated that the CoPOM loaded on MIL-101 displays enhanced activity and improved stability due to the its electrostatic interaction with MIL-101. In addition, the heterogenization of the homogeneous CoPOM also makes it easier to be recycled. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 89
页数:7
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