journal article·2016-11-15Open access

Tuning the Photoelectrocatalytic Hydrogen Evolution of Pt-Decorated Silicon Photocathodes by the Temperature and Time of Electroless Pt Deposition

Bruno Fabre, Gaozeng Li, Francis Gouttefangeas, Loic Joanny, Gabriel Loget

Langmuir· Volume 32· Issue 45

Abstract

The electroless deposition of Pt nanoparticles (NPs) on hydrogen-terminated silicon (H–Si) surfaces is studied as a function of the temperature and the immersion time. It is demonstrated that isolated Pt structures can be produced at all investigated temperatures (between 22 and 75 °C) for short deposition times, typically within 1–10 min if the temperature is 45 °C or less than 5 min at 75 °C. For longer times, dendritic metal structures start to grow, ultimately leading to highly rough interconnected Pt networks. Upon increasing the temperature from 22 to 75 °C and for an immersion time of 5 min, the average size of the observed Pt NPs monotonously increases from 120 to 250 nm, and their number density calculated using scanning electron microscopy decreases from (4.5 ± 1.0) × 10 8 to (2.0 ± 0.5) × 10 8 Pt NPs cm –2 . The impact of both the morphology and the distribution of the Pt NPs on the photoelectrocatalytic activity of the resulting metallized photocathodes is then analyzed. Pt deposited at 45 °C for 5 min yields photocathodes with the best electrocatalytic activity for the hydrogen evolution reaction. Under illumination at 33 mW cm –2, this optimized photoelectrode shows a fill factor of 45%, an efficiency (η) of 9.7%, and a short-circuit current density (| J sc |) at 0 V versus a reversible hydrogen electrode of 15.5 mA cm –2 .
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications · Chalcogenide Semiconductor Thin Films

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Matière Condensée et Systèmes Electroactifs (MaCSE), Institut des Sciences Chimiques de Rennes (ISCR), UMR 6226 CNRS and ‡ScanMAT−CMEBA, Université de Rennes 1, Campus de Beaulieu, 35042 Rennes Cedex, France

Funding

Centre National de la Recherche Scientifique · Université de Rennes 1

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