journal article·2020-11-04Open access

Increasing the Alkaline Stability of N,N-Diaryl Carbazolium Salts Using Substituent Electronic Effects

Nansi Gjineci, Sinai Aharonovich, Dario R. Dekel, Charles E. Diesendruck

ACS Applied Materials & Interfaces· Volume 12· Issue 44

Abstract

-diaryl carbazolium salts decompose through a single-electron-transfer mechanism, the change in carbazolium electron density leads to a very significant impact on their chemical stability. Substituents with very negative Hammett parameters demonstrate unparalleled stability toward dry hydroxide. This study provides guidelines for a different approach to develop stable quaternary ammonium salts for AEMFCs, making use of the unique parameters of this decomposition mechanism.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Fuel Cells and Related Materials · Electrocatalysts for Energy Conversion · Advanced battery technologies research

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

Affiliations

Schulich Faculty of Chemistry, Technion—Israel Institute of Technology, Haifa 3200008, Israel

The Wolfson Department of Chemical Engineering, Technion—Israel Institute of Technology, Haifa 3200003, Israel

The Nancy & Stephen Grand Technion Energy Program (GTEP), Technion—Israel Institute of Technology, Haifa 3200003, Israel

Funding

Israel Science Foundation · Ministry of National Infrastructure, Energy and Water Resources · Council for Higher Education · Horizon 2020 Framework Programme · Planning & Budgeting Committee · Fuel Choice Initiative

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