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Abstract Electrocatalytic proton reduction to form dihydrogen (H2) is an effective way to store energy in the form of chemical bonds. In this study, we validate the applicability of a main‐group‐element‐based tin porphyrin complex as an effective molecular electrocatalyst for proton reduction. A PEGylated Sn porphyrin complex (SnPEGP) displayed high activity (−4.6 mA cm−2at −1.7 V vs. Fc/Fc+) and high selectivity (H2Faradaic efficiency of 94 % at −1.7 V vs. Fc/Fc+) in acetonitrile (MeCN) with trifluoroacetic acid (TFA) as the proton source. The maximum turnover frequency (TOFmax) for H2production was obtained as 1099 s−1. Spectroelectrochemical analysis, in conjunction with quantum chemical calculations, suggest that proton reduction occurs via an electron‐chemical‐electron‐chemical (ECEC) pathway. This study reveals that the tin porphyrin catalyst serves as a novel platform for investigating molecular electrocatalytic reactions and provides new mechanistic insights into proton reduction.
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Hydrodechlorination of Alachlor Using a Molecular Electrocatalyst
Abstract Reductive hydrodechlorination is an effective approach to enhance the degradation rate of chlorinated herbicides such as alachlor, which are frequently detected in ground and surface water. In this study, a cobalt porphyrin complex with eight triazole units and alkyl chains,CoPor8T, was synthesized to catalyze the reductive hydrodechlorination of alachlor. Mechanistic study was performed using a combination of voltametric, spectroscopic, and electrospectroscopic techniques. A conversion yield of 84 % at −1.8 V vs. Fc/Fc+and chloride ion concentration of 96 % was obtained after electrocatalysis. This work provides a new avenue of using molecular catalysts for electrocatalytic chlorinated herbicide remediation.
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- Award ID(s):
- 2051260
- PAR ID:
- 10395861
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- ChemCatChem
- Volume:
- 15
- Issue:
- 5
- ISSN:
- 1867-3880
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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