Photocatalytic hydrogen production with alkylated nickel bis-dithiolene complexes

被引:19
|
作者
Zarkadoulas, Athanasios [1 ]
Koutsouri, Eugenia [1 ]
Semidalas, Emmanouil [1 ]
Psycharis, Vassilis [2 ]
Raptopoulou, Catherine P. [2 ]
Mitsopoulou, Christiana A. [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Dept Chem, Inorgan Chem Lab, Panepistimiopolis 15771, Zografou, Greece
[2] Natl Ctr Sci Res Demokritos, Inst Nanosci & Nanotechnol, Athens 15341, Greece
关键词
Photocatalysis; Bridged-complex; Nickel; Hydrogen; Dithiolene; RAY-ABSORPTION SPECTROSCOPY; ACTIVE-SITE MODEL; ELECTROCATALYTIC REDUCTION; ELECTRONIC-STRUCTURE; DIHYDROGEN FORMATION; METAL-COMPLEXES; NI DITHIOLENES; EVOLUTION; GENERATION; PROTONS;
D O I
10.1016/j.poly.2018.06.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein, we present the preparation and characterization of two nickel dithiolene complexes, namely [Ni(C-3(S2C2Ph2}(2))] (1) and [Ni(C-3{p-OMe-C6H4)(2))] (2). X-ray diffraction data for 2 collected on single crystals reveal that the complex is a neutral mononuclear entity with symmetric square planar geometry around the metal center. Electrochemical, photophysical, and theoretical studies have been employed to characterize and to probe both compounds under study in photoinduced hydrogen evolution experiments. Catalyst (2) performs better than catalyst (1), reaching 73 TONs over a 5 h period with [Ru(bpy)(3)]Cl-2 as photosensitizer, in MeCN-water solvent mixture with ascorbate at pH 4 as a sacrificial electron donor. The different catalytic activity between the two compounds is discussed based on their different electronic properties. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:138 / 146
页数:9
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