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一种打破基于多金属氧酸盐的金属有机框架以获得高负载量纳米级多金属氧酸盐簇以提高染料敏化太阳能电池性能的策略。

A Strategy for Breaking Polyoxometalate-based MOFs To Obtain High Loading Amounts of Nanosized Polyoxometalate Clusters to Improve the Performance of Dye-sensitized Solar Cells.

作者信息

Zheng Xiaotao, Chen Weilin, Chen Li, Wang Yijing, Guo Xiangwei, Wang Jiabo, Wang Enbo

机构信息

Key Laboratory of Polyoxometalate Science of Ministry of Education, Department of Chemistry, Northeast Normal University, Changchun, Jilin, 130024, P. R. China.

出版信息

Chemistry. 2017 Jul 3;23(37):8871-8878. doi: 10.1002/chem.201701103. Epub 2017 Apr 24.

Abstract

Polyoxometalates (POM) have already been confirmed to act as effective electron-transfer mediators for improving the power conversion efficiency (PCE) of dye-sensitized solar cells (DSSCs) based on previous studies. However, the improvement may be limited by the agglomeration of the polyoxoanions. In this paper, the previous synthesis strategy is improved upon by breaking the metal-organic frameworks (MOFs) with POMs as the secondary building units ([Ni(bpp)(H O) ] [P W O ]⋅24 H O (1) (bpp=1,3-bis(4-pyridyl)propane) and H [Cu (H O) (P W O ) (3-dpye) ]⋅28 H O (2) (3-dpye=N,N'-bis(3-pyridinecarboxamide)-1,2-ethane)) to design and synthesize small sized and highly disperse POM nanoparticles by means of compositing with TiO , through calcination to remove the organic ligand. TEM and element mapping confirm that P W O (denoted as P W ) nanoparticles with the diameter of ≈1 nm are uniformly distributed in TiO composites. The loading amount (wt. %) of POM in MOFs reaches 75.67 %. The small sized and highly disperse P W nanoparticles may provide more active sites and specific surface areas for improving the PCE of DSSCs. Finally, the investigations indicate that the PCE of composite P W ⋅NiO@TiO photoanodes is up to 7.56 %, which was 26 % higher than the pristine TiO based photoanodes.

摘要

基于先前的研究,多金属氧酸盐(POM)已被证实可作为有效的电子转移介质,用于提高染料敏化太阳能电池(DSSC)的功率转换效率(PCE)。然而,这种提高可能会受到多金属氧阴离子团聚的限制。在本文中,通过以POM作为二级结构单元([Ni(bpp)(H₂O)₆]₃[P₂W₁₈O₆₂]·24H₂O (1) (bpp = 1,3 - 双(4 - 吡啶基)丙烷)和H₆[Cu₃(H₂O)₆(P₂W₁₈O₆₂)(3 - dpye)₂]·28H₂O (2) (3 - dpye = N,N' - 双(3 - 吡啶甲酰胺)- 1,2 - 乙烷))破坏金属有机框架(MOF)来改进先前的合成策略,通过与TiO₂复合并煅烧以去除有机配体,从而设计并合成小尺寸且高度分散的POM纳米颗粒。透射电子显微镜(TEM)和元素映射证实,直径约为1 nm的P₂W₁₈O₆₂(记为P₂W)纳米颗粒均匀分布在TiO₂复合材料中。POM在MOF中的负载量(重量百分比)达到75.67%。小尺寸且高度分散的P₂W纳米颗粒可为提高DSSC的PCE提供更多活性位点和比表面积。最后,研究表明复合P₂W·NiO@TiO₂光阳极的PCE高达7.56%,比原始TiO₂基光阳极高26%。

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