In situ Stabilization of Au and Co Nanoparticles in a Redox-Active Conjugated Microporous Polymer Matrix: Facile Heterogeneous Catalysis and Electrocatalytic Oxygen Reduction Reaction Activity

Bhattacharyya, Sohini ; Samanta, Debabrata ; Roy, Syamantak ; Haveri Radhakantha, Vishnu Priya ; Maji, Tapas Kumar (2019) In situ Stabilization of Au and Co Nanoparticles in a Redox-Active Conjugated Microporous Polymer Matrix: Facile Heterogeneous Catalysis and Electrocatalytic Oxygen Reduction Reaction Activity ACS Applied Materials & Interfaces, 11 (5). pp. 5455-5461. ISSN 1944-8244

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Official URL: http://doi.org/10.1021/acsami.8b20610

Related URL: http://dx.doi.org/10.1021/acsami.8b20610

Abstract

We report a novel in situ method for synthesis of metal nanoparticles (NPs)–CMP (conjugated microporous polymer) composites based on a redox-active, donor–acceptor CMP, tris-(4-aminophenyl)amine (TPA)–perylenediimide (PDI). The TPA–PDI CMP, comprising triphenylamine as an electron donor and PDI as an acceptor, showed stable charge-separated state and semiconducting behavior. Further, TPA–PDI CMP has been exploited for in situ stabilization of metal (Au and Co) NPs, and two novel nanocomposites (Au@TPA–PDI and Co@TPA–PDI) were prepared. The catalytic reduction of nitro aryls to amino aryls was studied using Au@TPA–PDI, which showed excellent yields and fast kinetics. The CMP itself was found to show good activity as a metal-free oxygen reduction reaction (ORR) electrocatalyst with an onset potential of 0.82 V. Stabilizing merely 2.56 wt % Co nanoparticles in the CMP matrix improved the electrochemical ORR activity of as-synthesized TPA–PDI immensely and showed an onset potential of 0.91 V, which has also been supported by density functional theory (DFT) calculations.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:124018
Deposited On:29 Oct 2021 09:41
Last Modified:29 Oct 2021 09:41

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