(5g) A New System of Electrochemical Oxidation Conversion of Biomass Coupled with Electrochemical Reduction of Carbon Dioxide to Formic Acid
AIChE Annual Meeting
2024
2024 AIChE Annual Meeting
Catalysis and Reaction Engineering Division
Biomass Conversion and Biorefining I: Platform Molecule Conversion
Sunday, October 27, 2024 - 5:18pm to 5:36pm
Therefore, in this work, we developed a facile method of electrodeposition based on chelating agents for preparing two-dimensional nanosheet electrocatalysts on both the anode and cathode. The anode electrocatalyst is prepared using electrodeposition method assisted with different chelating agent. It was found that the Ni-based electrocatalyst prepared by using EDTA2Na had the best performance for electrooxidation of biomass derived aldehydes (e.g. 5-hydroxymethylfurfural (HMF)). When the ratio of Ni2+ to EDTA2Na is 1:0.25, the electrocatalyst is dispersed scaly structure, which can achieve a high yield of 96.2% for FDCA and 96.7% for FEFDCA. The Ni-0.25EDTA2Na electrocatalyst can be stably cycled six time.
In the cathode, Bi-based electrocatalysts prepared by electrodeposition with different chelating agents have different morphologies. Bi-EDTA2Na has two-dimensional sheets with nano-corrugated paper morphology, which can achieve the FEHCOO- of 96% and the current density of 60mA/cm2. In the wide voltage range, the FEHCOO- of Bi-EDTA2Na is greater than 90%. Bi-EDTA2Na can be stably cycled for 24h. The current density of CO2RR to HCOOH can be further improved by using flow cell. And we prove BiO2CO3 is the active species.
Compared with the traditional OER-CO2RR coupling system, the new system can reduce the energy by 7.02%. The value of FDCA produced by the anode HMFOR is greatly increased by hundreds of times compared with the traditional system of OER. This work developed a renewable electricity-driven new system of biomass electrooxidation coupled with CO2RR.