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High-yield electrochemical production of formaldehyde from CO2 and seawater.

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TLDR
This work presents their work on the electrochemical reduction of CO2 in seawater using a boron-doped diamond (BDD) electrode under ambient conditions to produce formaldehyde, which overcomes the usual limitation of the low yield of higher-order products, and also reduces the generation of H2.
Abstract
The catalytic, electrocatalytic, or photocatalytic conversion of CO2 into useful chemicals in high yield for industrial applications has so far proven difficult. Herein, we present our work on the electrochemical reduction of CO2 in seawater using a boron-doped diamond (BDD) electrode under ambient conditions to produce formaldehyde. This method overcomes the usual limitation of the low yield of higher-order products, and also reduces the generation of H2 . In comparison with other electrode materials, BDD electrodes have a wide potential window and high electrochemical stability, and, moreover, exhibit very high Faradaic efficiency (74%) for the production of formaldehyde, using either methanol, aqueous NaCl, or seawater as the electrolyte. The high Faradaic efficiency is attributed to the sp(3)-bonded carbon of the BDD. Our results have wide ranging implications for the efficient and cost-effective conversion of CO2.

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Cu and Cu-Based Nanoparticles: Synthesis and Applications in Catalysis.

TL;DR: A critical appraisal of different synthetic approaches to Cu and Cu-based nanoparticles and copper nanoparticles immobilized into or supported on various support materials (SiO2, magnetic support materials, etc.), along with their applications in catalysis.
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Cocatalysts for Selective Photoreduction of CO2 into Solar Fuels.

TL;DR: Various cocatalysts, such as the biomimetic, metal-based,Metal-free, and multifunctional ones, and their selectivity for CO2 photoreduction are summarized and discussed, along with the recent advances in this area.
Journal ArticleDOI

Rational catalyst and electrolyte design for CO2 electroreduction towards multicarbon products

TL;DR: In this article, the authors discuss strategies to achieve high selectivity towards multicarbon products via rational catalyst and electrolyte design, focusing on findings extracted from in situ and operando characterizations.
Journal ArticleDOI

Nanostructured Materials for Heterogeneous Electrocatalytic CO2 Reduction and their Related Reaction Mechanisms

TL;DR: Recent progress on the design and synthesis of solid-state catalysts for the electrochemical reduction of CO2 is described, followed by the general parameters for CO2 electroreduction and a summary of the reaction apparatus.
Journal ArticleDOI

Modern Electrochemical Aspects for the Synthesis of Value-Added Organic Products.

TL;DR: This Review surveys many of the recent seminal important developments which will determine the future of this dynamic emerging field of organic synthesis.
References
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Journal ArticleDOI

Ionic Liquid–Mediated Selective Conversion of CO2 to CO at Low Overpotentials

TL;DR: An electrocatalytic system that reduces CO2 to carbon monoxide (CO) at overpotentials below 0.2 volt is reported, and the system continued producing CO for at least 7 hours at Faradaic efficiencies greater than 96%.
BookDOI

Carbon dioxide as chemical feedstock

TL;DR: Aresta et al. as discussed by the authors discussed the potential for CO 2 reuse in the context of reducing CO 2 emissions in the atmosphere by using CO 2 as an inert solvent for chemical synthesis.
Journal ArticleDOI

Ligand-Enabled Reactivity and Selectivity in a Synthetically Versatile Aryl C–H Olefination

TL;DR: An operationally simple, atom-economical, carboxylate-directed Pd(II)-catalyzed C–H olefination reaction with phenylacetic acid and 3-phenylpropionic acid substrates, using oxygen at atmospheric pressure as the oxidant.
Journal ArticleDOI

Integrated Electromicrobial Conversion of CO2 to Higher Alcohols

TL;DR: This work genetically engineered a lithoautotrophic microorganism, Ralstonia eutropha H16, to produce isobutanol and 3-methyl-1-butanol in an electro-bioreactor, opening the possibility of electricity-driven bioconversion of CO2 to commercial chemicals.
Journal ArticleDOI

Electrocatalytic CO2 conversion to oxalate by a copper complex.

TL;DR: A dinuclear Copper(I) complex that is oxidized in air by CO2 rather than O2 is described; the product is a tetranuclear copper(II) complex containing two bridging CO2-derived oxalate groups, which can be nearly quantitatively electrochemically reduced at a relatively accessible potential, regenerating the initial dinuclear copper (I) compound.
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