Engaging Dynamic Surfactant Assemblies in Improving Metal Ion Sensitivity of a 1,4,7-Triazacyclononane-Based Receptor: Differential Optical Response for Cysteine and Histidine

Maiti, Bappa ; Dey, Nilanjan ; Bhattacharya, Santanu (2019) Engaging Dynamic Surfactant Assemblies in Improving Metal Ion Sensitivity of a 1,4,7-Triazacyclononane-Based Receptor: Differential Optical Response for Cysteine and Histidine ACS Applied Bio Materials, 2 (6). pp. 2365-2373. ISSN 2576-6422

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Official URL: http://doi.org/10.1021/acsabm.9b00083

Related URL: http://dx.doi.org/10.1021/acsabm.9b00083

Abstract

Oxygen evolution reaction (OER) is energetically challenging from the platform of making many photovoltaic devices such as metal-air batteries and water splitting systems because of its poor kinetics even when precious metals are used. Herein, a Co(II)-porphyrin/pyrene-comprised conjugated microporous polymer Co-MPPy-1 has been developed which shows efficient OER in alkaline medium. The material was characterized by Fourier transform infrared, solid-state 13C cross-polarization magic angle spinning nuclear magnetic resonance, N2 volumetric adsorption/desorption analysis, scanning electron microscopy, ultra high resolution-transmission electron microscopy, X-ray photoelectron spectroscopy, and other physical studies. Co-MPPy-1 showed Brunauer-Emmett-Teller surface area of ∼501 m2 g-1. Co-MPPy-1 achieved a current density of 1 and 10 mA/cm-2 at 340 and 420 mV, respectively. The turnover frequency calculated for the OER is 0.43 s-1. The heterogeneity of this electrocatalyst was tested by chronoamperometric measurement and 1000 cycle recyclability test with retainment of the excellent electrochemical catalytic activity. This can be attributed to the presence of high density of Co(II) porphyrin unit and efficient charge transport in the π-conductive conjugated polymeric backbone.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:134262
Deposited On:05 Jan 2023 11:37
Last Modified:05 Jan 2023 11:37

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