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T. Jane Stockmann

Researcher at Paris Diderot University

Publications -  21
Citations -  362

T. Jane Stockmann is an academic researcher from Paris Diderot University. The author has contributed to research in topics: Chemistry & ITIES. The author has an hindex of 11, co-authored 13 publications receiving 263 citations. Previous affiliations of T. Jane Stockmann include University of Western Ontario & École Polytechnique Fédérale de Lausanne.

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Journal ArticleDOI

Gold Nanofilms at Liquid-Liquid Interfaces: An Emerging Platform for Redox Electrocatalysis, Nanoplasmonic Sensors, and Electrovariable Optics.

Micheál D. Scanlon, +3 more
- 30 Jan 2018 - 
TL;DR: The ability of floating gold nanofilms to impact a diverse range of fields is demonstrated: in particular, redox electrocatalysis, surface-enhanced Raman spectroscopy (SERS) or surface plasmon resonance (SPR) based sensors, and electrovariable optical devices.
Journal ArticleDOI

Platinum Nanoparticle Impacts at a Liquid|Liquid Interface

T. Jane Stockmann, +4 more
- 16 Oct 2017 - 
TL;DR: Current spikes reminiscent of nanoimpacts were recorded, which corresponded to electrocatalytic enhancement of the ORR by Pt NPs, which allowed exploration of new phenomena in single NP electrochemistry.
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Decamethylruthenocene Hydride and Hydrogen Formation at Liquid|Liquid Interfaces

Lucie Rivier, +8 more
- 05 Nov 2015 - 
TL;DR: In this paper, the authors describe a unique platform for evaluating the kinetics/thermodynamics for metallocene hydride formation using decamethylruthenocene.
Journal ArticleDOI

Electrochemical oxygen reduction at soft interfaces catalyzed by the transfer of hydrated lithium cations

Haiqiang Deng, +4 more
- 01 Oct 2014 - 
TL;DR: In this article, the oxygen reduction reaction by decamethylferrocene (DMFc), triggered by hydrophilic metallic cations behaving as Lewis acids towards water molecules in a homogeneous organic phase reaction, was investigated using cyclic voltammetry at the water|1,2-dichloroethane (w|DCE) interface.
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Surprising acidity of hydrated lithium cations in organic solvents.

Haiqiang Deng, +8 more
- 29 Apr 2014 - 
TL;DR: It is proposed that this catalytic effect is due to the surprising acidity of the hydrated cations; interactions between the cation and its surrounding solvation shell will make the constituent water molecules more acidic.