Layered Noble Metal Dichalcogenides: Tailoring Electrochemical and Catalytic Properties

Xinyi Chia; Zdeněk Sofer; Jan Luxa; Martin Pumera

doi:10.1021/acsami.7b05083

Layered Noble Metal Dichalcogenides: Tailoring Electrochemical and Catalytic Properties

ACS Appl Mater Interfaces. 2017 Aug 2;9(30):25587-25599. doi: 10.1021/acsami.7b05083. Epub 2017 Jul 19.

Authors

Xinyi Chia¹, Zdeněk Sofer², Jan Luxa², Martin Pumera¹

Affiliations

¹ Division of Chemistry & Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University , Singapore 637371, Singapore.
² Department of Inorganic Chemistry, University of Chemistry and Technology Prague , Technická 5, 166 28 Prague 6, Czech Republic.

PMID: 28722402
DOI: 10.1021/acsami.7b05083

Abstract

Owing to the anisotropic nature, layered transition metal dichalcogenides (TMDs) have captured tremendous attention for their promising uses in a plethora of applications. Currently, bulk of the research is centered on Group 6 TMDs. Layered noble metal dichalcogenides, in particular the noble metal tellurides, belong to a subset of Group 10 TMDs, wherein the transition metal is a noble metal of either palladium or platinum. We address here a lack of contemporary knowledge on these compounds by providing a comprehensive study on the electrochemistry of layered noble metal tellurides, PdTe₂ and PtTe₂, and their efficiency as electrocatalysts toward the hydrogen evolution reaction (HER). Observed parallels in the electrochemical peaks of the noble metal tellurides are traced to the tellurium electrochemistry. PdTe₂ and PtTe₂ can be discriminated by their distinct reduction peaks in the first cathodic scans. Considering the influence of the metal component, PtTe₂ outperforms PdTe₂ in aspects of charge transfer and electrocatalysis. The heterogeneous electron transfer (HET) rate of PtTe₂ is an order of magnitude faster than PdTe₂, and a lower HER overpotential of 0.54 V versus reversible hydrogen electrode (RHE) at a current density of -10 mA cm^-2 is evident in PtTe₂. On PdTe₂ and PtTe₂ surfaces, adsorption via the Volmer process has been identified as the limiting step for HER. A general phenomenon for the noble metal tellurides is that faster HET rates are observed upon electrochemical reductive pretreatment, whereas slower HET rates occur when the noble metal tellurides are oxidized during pretreatment. PtTe₂ becomes successfully activated for HER when subject to oxidative treatment, whereas oxidized or reduced PdTe₂ shows a deactivated HER performance. These findings provide fundamental insights that are pivotal to advancing the field of the underemphasized TMDs. Furthermore, electrochemical tuning as a means to tailor specific properties of the TMDs is advantageous for the development of their future applications.

Keywords: electrochemical activation; electrochemistry; electron transfer; hydrogen evolution; layered; palladium telluride; platinum telluride.