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Autor(en) / Beteiligte
Titel
A conductive catecholate-based framework coordinated with unsaturated bismuth boosts CO electroreduction to formate
Ist Teil von
  • Chemical science (Cambridge), 2023-06, Vol.14 (25), p.686-6866
Erscheinungsjahr
2023
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • Bismuth-based metal-organic frameworks (Bi-MOFs) have received attention in electrochemical CO 2 -to-formate conversion. However, the low conductivity and saturated coordination of Bi-MOFs usually lead to poor performance, which severely limits their widespread application. Herein, a conductive catecholate-based framework with Bi-enriched sites (HHTP, 2,3,6,7,10,11-hexahydroxytriphenylene) is constructed and the zigzagging corrugated topology of Bi-HHTP is first unraveled via single-crystal X-ray diffraction. Bi-HHTP possesses excellent electrical conductivity (1.65 S m −1 ) and unsaturated coordination Bi sites are confirmed by electron paramagnetic resonance spectroscopy. Bi-HHTP exhibited an outstanding performance for selective formate production of 95% with a maximum turnover frequency of 576 h −1 in a flow cell, which surpassed most of the previously reported Bi-MOFs. Significantly, the structure of Bi-HHTP could be well maintained after catalysis. In situ attenuated total reflectance Fourier transform infrared spectroscopy (ATR-FTIR) confirms that the key intermediate is *COOH species. Density functional theory (DFT) calculations reveal that the rate-determining step is *COOH species generation, which is consistent with the in situ ATR-FTIR results. DFT calculations confirmed that the unsaturated coordination Bi sites acted as active sites for electrochemical CO 2 -to-formate conversion. This work provides new insights into the rational design of conductive, stable, and active Bi-MOFs to improve their performance towards electrochemical CO 2 reduction. A conductive MOF, named Bi-based catecholate BiHHTP, exhibited excellent catalytic performance towards CO 2 electroreduction.
Sprache
Identifikatoren
ISSN: 2041-6520
eISSN: 2041-6539
DOI: 10.1039/d3sc01876h
Titel-ID: cdi_rsc_primary_d3sc01876h
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