MFC-driven H2S electro-oxidation based on Fe nanoparticles anchored on carbon aerogel-ZIF-8: a combined experimental and DFT study
Electrocatalysts for the electrochemical oxidation of hydrogen sulfide (H2S) to elemental sulfur and its recovery in the form of sulfur, particularly catalysts based on metal–organic-framework (MOF) supports, have been widely investigated. However, energy saving during the electrochemical oxidation...
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Published in | Journal of materials chemistry. C, Materials for optical and electronic devices Vol. 10; no. 4; pp. 1421 - 1435 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
28.01.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Electrocatalysts for the electrochemical oxidation of hydrogen sulfide (H2S) to elemental sulfur and its recovery in the form of sulfur, particularly catalysts based on metal–organic-framework (MOF) supports, have been widely investigated. However, energy saving during the electrochemical oxidation of H2S, the formation of a catalyst with superb conductivity and stability by protecting a zeolitic imidazolate framework-8 (ZIF-8) from being destroyed during synthesis, and the prevention of Fe sites from deactivation are still challenging tasks. Herein, an effective strategy to improve the crystalline structure and enhance the porosity/surface area of ZIF-8 with poor crystallinity by the induced growth of a carbon aerogel (CA)-ZIF-8 on a mixed-metal metal–organic framework (MM-MOF) template with good crystallinity and optimized Fe nanoparticle doping content (1, 3, and 5 wt%) is described. Moreover, a microbial fuel cell (MFC) with different cathode catalysts was started up and operated to provide the electrical energy to drive the electrocatalytic removal of H2S. Through open-circuit voltage (OCV) and anodic polarization measurements at 0.2, 0.5, and 0.7 V vs. the standard hydrogen electrode (SHE), the Fe-doped CAs-ZIF-8@MM-MOF (1 wt%) exhibits excellent electro-catalytic activity (8.12 ± 0.11 h−1 at 0.7 V vs. SHE) compared to a pristine carbon cloth (CC) electrode (1.13 ± 0.24 h−1 at 0.7 V vs. SHE). According to surface characterization and density functional theory (DFT) calculation results, it is worth noting that the introduction of a low loading of Fe nanoparticles into a catalyst support prefers to occupy an Fe–N4 configuration rather than an M–Fe–M (C) configuration. The Fe–N4 active centers favor the adsorption and association/dissociation of H2S. In contrast, the M–Fe–M (C) centers are more favorable for strengthening the bonding between the Fe nanoparticles and the support. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d1tc03877j |