Highly Stable Self‐Regenerating Organic Multi‐Redox Systems derived from Bicyclic (Alkyl)(amino)carbenes (BICAACs)

Author:

Das Arpan1ORCID,Saha Sukanta2ORCID,Maji Subir1ORCID,Sarkar Pallavi3,Jose Anex1ORCID,Bhatt Madhur Mahesh1,Bhunia Anup1,Dutta Arnab2ORCID,Pati Swapan K.3ORCID,Mandal Swadhin K.1ORCID

Affiliation:

1. Department of Chemical Sciences Indian Institute of Science Education and Research Kolkata Mohanpur 741246 Nadia India.

2. Chemistry Department Indian Institute of Technology Bombay Powai Mumbai 400076 India

3. Theoretical Sciences Unit Jawaharlal Nehru Center for Advanced Scientific Research Bangalore 560064 India.

Abstract

AbstractAn extended class of organic multi‐redox systems was derived from bicyclic(alkyl)amino carbenes (BICAACs). The highly‐conjugated system undergoes a total of 4 redox events spanning a 1.8 V redox range. These organic compounds exhibited four different stable redox states (dication, radical cation, neutral and radical anion), and all of them were characterized either by single crystal X‐ray study and/or various spectroscopic studies. Three of the four redox states are stable to air and moisture. The availability of stable multiple redox states demonstrated promise towards their efficacy in the symmetric H‐cell charge/discharge cycling. Among various redox states, the dication/neutral state works efficiently and continuously for 1500 cycles in 2e charge/discharge process outside glovebox in commercially available DMF with minimum capacity loss (retaining nearly 90 % Coulombic efficiency). Surprisingly, the efficiency of the redox cycle was retained even if the system was exposed to air for 30 days when it slowly regenerated to the initial deep blue radical cation, and it exhibited another 100 charge/discharge cycles with a minimal capacity loss. Such a stable H‐cell cycling ability is not well known among organic molecule‐based systems.

Funder

Science and Engineering Research Board

Publisher

Wiley

Reference58 articles.

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