Issue 18, 2013

Ruthenium core-activated platinum monolayer shell high redox activity cathodic electrocatalysts for dye-sensitized solar cells

Abstract

Here, we have combined the understanding of density functional theory in relation with lattice strain-to-activity correlation to design a Rucore–Ptshell structured electrocatalyst in a dye-sensitized solar cell (DSC) cathode. This electrocatalyst possesses a compressive lattice strain in the shell region which translocates the Pt valence charge to neighboring atoms to decrease the Pt valence band density of states and thus lower the Pt d-band levels. Consequently, compared with DSCs using Pt nanoparticles (NPs) cathode, the Rucore–Ptshell NPs improves the triiodide to iodide redox reduction activity by 2.11-fold and thus boosts the photovoltaic efficiency of DSCs by ∼30.4%. These results provide mechanistic information for the development of DSCs with reduced Pt utilization and programmable electrochemical performance.

Graphical abstract: Ruthenium core-activated platinum monolayer shell high redox activity cathodic electrocatalysts for dye-sensitized solar cells

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2012
Accepted
05 Mar 2013
First published
05 Mar 2013

J. Mater. Chem. A, 2013,1, 5660-5669

Ruthenium core-activated platinum monolayer shell high redox activity cathodic electrocatalysts for dye-sensitized solar cells

T. Chen, Y. Liu, H. M. Nguyen, L. Fan, C. Wu, T. Mark Luo, C. Lee, Y. Yang, T. Wen and T. Lin, J. Mater. Chem. A, 2013, 1, 5660 DOI: 10.1039/C3TA01547E

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