Enhanced light-induced hydrogen evolution reaction by supramolecular systems of cobalt(II) and copper(II) octaethylporphyrins on glassy carbon electrodes

被引:16
作者
Canales, Camila [1 ]
Olea, Andres F. [2 ]
Gidi, Leyla [1 ]
Arce, Roxana [3 ]
Ramirez, Galo [1 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Quim, Dept Quim Inorgan, Av Vicuna Mackenna 4860,Casilla 306,Correo 22, Santiago, Chile
[2] Univ Autonoma Chile, Fac Ingn, Inst Ciencias Quim Aplicadas, Llano Subercaseuax 2801, Santiago, Chile
[3] Univ Santiago Chile USACH, Fac Quim & Biol, Dept Quim Mat, Av LB OHiggins 3363, Santiago, Chile
关键词
Hydrogen evolution reaction; Metalloporphyrins; Modified electrodes; Supramolecular system; Photoelectrocatalysis; OXYGEN REDUCTION; AQUEOUS-SOLUTION; PORPHYRIN; CATALYSIS; COMPLEXES; WATER; METALLOPORPHYRINS; PHTHALOCYANINES; ASSEMBLIES; GENERATION;
D O I
10.1016/j.electacta.2017.11.135
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Chemically modified glassy carbon electrodes formed by p-stacking of commercial cobalt (II) and copper (II) porphyrins have been used as stable and efficient electrocatalytic system for the hydrogen evolution reaction at pH 7.0, as reported in a previous work. In this work, it has been found that when these systems are irradiated with light of different wavelengths, their electrocatalytic responses change in terms of overpotential and photocurrent. Thus, the electroactivity of these systems towards hydrogen evolution reaction can be enhanced by irradiation at certain wavelength with no requirement of a photosensitizer. Interestingly, the largest enhancement of this reaction is observed at wavelengths corresponding to specific arrangement of porphyrins on the electrode. Cyclic voltammetry, photo-electrochemical impedance spectroscopy and UV-visible spectroscopy studies were done in order to corroborate and discuss this effect. Finally, XRD experiments allowed us to confirm the existence of highly ordered arrangement in each supramolecular system and that this is a determinant factor in the photoelectrochemical responses. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:850 / 857
页数:8
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