Direct Electroreduction of Carbonate to Formate.

A cause of losses in energy and carbon conversion efficiencies during the electrochemical CO2 reduction reaction (eCO2RR) can be attributed to the formation of carbonates (CO32-), which is generally considered to be an electrochemically inert species. Herein, using in situ Raman spectroscopy, liquid chromatography, 1H nuclear magnetic resonance spectroscopy, 13C and deuterium isotope labeling, and density functional theory simulations, we show that carbonate intermediates are adsorbed on a copper electrode during eCO2RR in KHCO3 electrolyte from 0.2 to -1.0 VRHE. These intermediates can be reduced to formate at -0.4 VRHE and more negative potentials. This finding is supported by our observation of formate from the reduction of Cu2(CO3)(OH)2. Pulse electrolysis on a copper electrode immersed in a N2-purged K2CO3 electrolyte was also performed. We found that the carbonate anions therein could be first adsorbed at -0.05 VRHE and then directly reduced to formate at -0.5 VRHE (overpotential of 0.28 V) with a Faradaic efficiency of 0.61%. The nature of the active sites generating the adsorbed carbonate species and the mechanism for the pulse-enabled reduction of carbonate to formate were elucidated. Our findings reveal how carbonates are directly reduced to a high-value product such as formate and open a potential pathway to mitigate carbonate formation during eCO2RR.

NMR-based quantification of liquid products in CO2 electroreduction on phosphate-derived nickel catalysts.

Recently discovered phosphate-derived Ni catalysts have opened a new pathway towards multicarbon products via CO2 electroreduction. However, understanding the influence of basic parameters such as electrode potential, pH, and buffer capacity is needed for optimized C3+ product formation. To this end, rigorous catalyst evaluation and sensitive analytical tools are required to identify potential new products and minimize increasing quantification errors linked to long-chain carbon compounds. Herein, we contribute to enhance testing accuracy by presenting sensitive 1H NMR spectroscopy protocols for liquid product assessment featuring optimized water suppression and reduced experiment time. When combined with an automated NMR data processing routine, samples containing up to 12 products can be quantified within 15 min with low quantification limits equivalent to Faradaic efficiencies of 0.1%. These developments disclosed performance trends in carbon product formation and the detection of four hitherto unreported compounds: acetate, ethylene glycol, hydroxyacetone, and i-propanol.

Enhanced Carbon Monoxide Electroreduction to >1†A cm-2 C2+ Products Using Copper Catalysts Dispersed on MgAl Layered Double Hydroxide Nanosheet House-of-Cards Scaffolds.

Cu catalysts are most apt for reducing CO(2) to multi-carbon products in aqueous electrolytes. To enhance the product yield, we can increase the overpotential and the catalyst mass loading. However, these approaches can cause inadequate mass transport of CO(2) to the catalytic sites, which will then lead to H2 evolution dominating the product selectivity. Herein, we use a MgAl LDH nanosheet 'house-of-cards' scaffold to disperse CuO-derived Cu (OD-Cu). With this support-catalyst design, at -0.7 VRHE , CO could be reduced to C2+ products with a current density (jC2+ ) of -1251 mA cm-2 . This is 14× that of the jC2+ shown by unsupported OD-Cu. The current densities of C2+ alcohols and C2 H4 were also high at -369 and -816 mA cm-2 respectively. We propose that the porosity of the LDH nanosheet scaffold enhances CO diffusion through the Cu sites. The CO reduction rate can thus be increased, while minimizing H2 evolution, even when high catalyst loadings and large overpotentials are used.

Surface charge as activity descriptors for electrochemical CO2 reduction to multi-carbon products on organic-functionalised Cu.

Intensive research in electrochemical CO2 reduction reaction has resulted in the discovery of numerous high-performance catalysts selective to multi-carbon products, with most of these catalysts still being purely transition metal based. Herein, we present high and stable multi-carbon products selectivity of up to 76.6% across a wide potential range of 1 V on histidine-functionalised Cu. In-situ Raman and density functional theory calculations revealed alternative reaction pathways that involve direct interactions between adsorbed histidine and CO2 reduction intermediates at more cathodic potentials. Strikingly, we found that the yield of multi-carbon products is closely correlated to the surface charge on the catalyst surface, quantified by a pulsed voltammetry-based technique which proved reliable even at very cathodic potentials. We ascribe the surface charge to the population density of adsorbed species on the catalyst surface, which may be exploited as a powerful tool to explain CO2 reduction activity and as a proxy for future catalyst discovery, including organic-inorganic hybrids.

Surface Water as an Initial Proton Source for the Electrochemical CO Reduction Reaction on Copper Surfaces.

We have employed in situ electrochemical shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS) and density functional theory (DFT) calculations to study the CO reduction reaction (CORR) on Cu single-crystal surfaces under various conditions. Coadsorbed and structure-/potential-dependent surface species, including *CO, Cu-Oad , and Cu-OHad , were identified using electrochemical spectroscopy and isotope labeling. The relative abundance of *OH follows a "volcano" trend with applied potentials in aqueous solutions, which is yet absent in absolute alcoholic solutions. Combined with DFT calculations, we propose that the surface H2 O can serve as a strong proton donor for the first protonation step in both the C1 and C2 pathways of CORR at various applied potentials in alkaline electrolytes, leaving adsorbed *OH on the surface. This work provides fresh insights into the initial protonation steps and identity of key interfacial intermediates formed during CORR on Cu surfaces.

Production of C3 -C6 Acetate Esters via CO Electroreduction in a Membrane Electrode Assembly Cell.

Electrocatalytic carbon monoxide reduction has been previously reported to yield a range of carbonaceous products including alcohols, hydrocarbons and carboxylic acids. However, esters, an important family of organic compounds, have not been formed. Herein, we report the electrosynthesis of C3 to C6 acetate esters (H3 C-(C=O)-O-R) from carbon monoxide using copper catalysts in a membrane electrode assembly cell. Ethyl acetate and propyl acetate could be produced with an unprecedented total Faradaic efficiency (FE) of ∼22 % and with a current density of up to -55 mA cm-2 , alongside minor quantities of methyl acetate and butyl acetate. The esters are produced via the addition reaction of ethenone (H2 C=C=O) and alcohols produced during CO reduction. We show that the near water-free reaction conditions and the high local pH play key roles in the formation of the esters.

Polaron Delocalization Dependence of the Conductivity and the Seebeck Coefficient in Doped Conjugated Polymers.

Conjugated polymers are promising materials for thermoelectrics as they offer good performances at near ambient temperatures. The current focus on polymer thermoelectric research mainly targets a higher power factor (PF; a product of the conductivity and square of the Seebeck coefficient) through improving the charge mobility. This is usually accomplished via structural modification in conjugated polymers using different processing techniques and doping. As a result, the structure-charge transport relationship in conjugated polymers is generally well-established. In contrast, the relationship between the structure and the Seebeck coefficient is poorly understood due to its complex nature. A theoretical framework by David Emin (Phys. Rev. B, 1999, 59, 6205-6210) suggests that the Seebeck coefficient can be enhanced via carrier-induced vibrational softening, whose magnitude is governed by the size of the polaron. In this work, we seek to unravel this relationship in conjugated polymers using a series of highly identical pro-quinoid polymers. These polymers are ideal to test Emin's framework experimentally as the quinoid character and polaron delocalization in these polymers can be well controlled even by small atomic differences (<10 at. % per repeating unit). By increasing the polaron delocalization, that is, the polaron size, we demonstrate that both the conductivity and the Seebeck coefficient (and hence PF) can be increased simultaneously, and the latter is due to the increase in the polaron's vibrational entropy. By using literature data, we also show that this phenomenon can be observed in two closely related diketopyrrolopyrrole-conjugated polymers as well as in p-doped P3HT and PANI systems with an increasing molecular order.

Mechanistic Insights into the Selective Electroreduction of Crotonaldehyde to Crotyl Alcohol and 1-Butanol.

The electroreduction of crotonaldehyde, which can be derived from the aldol condensation of acetaldehyde (sustainably produced from CO2 reduction or from biomass ethanol), is potentially a carbon-neutral route for generating high-value C4 chemicals such as crotyl alcohol and 1-butanol. Developing functional catalysts is necessary toward this end. Herein, the electrocatalytic conversion of crotonaldehyde to crotyl alcohol and 1-butanol was achieved in 0.1 m potassium phosphate buffer electrolyte (pH=7). More importantly, the mechanisms and structure-activity relationships of these transformations were elucidated. Crotyl alcohol was formed on oxide-derived Ag at -0.75 V versus the reversible hydrogen electrode (RHE) with a faradaic efficiency (FE) of 84.3 % (reactant conversion after 75 min electrolysis=9.8 %), which is 1.6 times higher than that on polished Ag foils. The coordinatively-unsaturated sites on oxide-derived Ag surfaces were proposed to facilitate crotonaldehyde adsorption via its oxygen atom in order to promote crotyl alcohol formation. On electrodeposited Fe nanoflakes, crotonaldehyde could be reduced to 1-butanol with an outstanding FE of 60.6 % (reactant conversion after 75 min electrolysis=9.4 %) at -0.70 V vs. RHE. This is nearly 3 times higher than the FE of 1-butanol observed on polished Fe foils at the same potential. More strikingly, the corresponding partial current density of 1-butanol was -9.19 mA cm-2 , which is 43 times higher than that on Fe foils. The presence of tensile strains and grain boundaries on the Fe nanoflakes were elucidated and suggested to activate a concerted reduction of the C=O and C=C bonds in crotonaldehyde to produce 1-butanol selectively.

Selectivity Map for the Late Stages of CO and CO2 Reduction to C2 Species on Copper Electrodes.

The electrochemical CO and CO2 reduction reactions (CORR and CO2 RR) using copper catalysts and renewable electricity hold promise as a carbon-neutral route to produce commodity chemicals and fuels. However, the exact mechanisms and structure sensitivity of Cu electrodes toward C2 products are still under debate. Herein, we investigate ethylene oxide reduction (EOR) as a proxy to the late stages of CORR to ethylene, and the results are compared to those of acetaldehyde reduction to ethanol. Density functional theory (DFT) calculations show that ethylene oxide undergoes ring opening before exclusively reducing to ethylene via *OH formation. Based on generalized coordination numbers (CN), a selectivity map for the late stages of CORR and CO2 RR shows that sites with moderate coordination (5.9 < CN < 7.5) are efficient for ethylene production, with pristine Cu(100) being more active than defective surfaces such as Cu(311). In contrast, kinks and edges are more active for ethanol production, while (111) terraces are relatively inert.

Electrochemical Reduction of Carbon Dioxide to 1-Butanol on Oxide-Derived Copper.

The electroreduction of carbon dioxide using renewable electricity is an appealing strategy for the sustainable synthesis of chemicals and fuels. Extensive research has focused on the production of ethylene, ethanol and n-propanol, but more complex C4 molecules have been scarcely reported. Herein, we report the first direct electroreduction of CO2 to 1-butanol in alkaline electrolyte on Cu gas diffusion electrodes (Faradaic efficiency=0.056 %, j1-Butanol =-0.080 mA cm-2 at -0.48 V vs. RHE) and elucidate its formation mechanism. Electrolysis of possible molecular intermediates, coupled with density functional theory, led us to propose that CO2 first electroreduces to acetaldehyde-a key C2 intermediate to 1-butanol. Acetaldehyde then undergoes a base-catalyzed aldol condensation to give crotonaldehyde via electrochemical promotion by the catalyst surface. Crotonaldehyde is subsequently electroreduced to butanal, and then to 1-butanol. In a broad context, our results point to the relevance of coupling chemical and electrochemical processes for the synthesis of higher molecular weight products from CO2 .

Enhanced Electroreduction of Carbon Dioxide to Methanol Using Zinc Dendrites Pulse-Deposited on Silver Foam.

The electrocatalytic CO2 reduction reaction (CO2 RR) can dynamise the carbon cycle by lowering anthropogenic CO2 emissions and sustainably producing valuable fuels and chemical feedstocks. Methanol is arguably the most desirable C1 product of CO2 RR, although it typically forms in negligible amounts. In our search for efficient methanol-producing CO2 RR catalysts, we have engineered Ag-Zn catalysts by pulse-depositing Zn dendrites onto Ag foams (PD-Zn/Ag foam). By themselves, Zn and Ag cannot effectively reduce CO2 to CH3 OH, while their alloys produce CH3 OH with Faradaic efficiencies of approximately 1 %. Interestingly, with nanostructuring PD-Zn/Ag foam reduces CO2 to CH3 OH with Faradaic efficiency and current density values reaching as high as 10.5 % and -2.7 mA cm-2 , respectively. Control experiments and DFT calculations pinpoint strained undercoordinated Zn atoms as the active sites for CO2 RR to CH3 OH in a reaction pathway mediated by adsorbed CO and formaldehyde. Surprisingly, the stability of the *CHO intermediate does not influence the activity.

Mechanistic Study of the Synergy between Iron and Transition Metals for the Catalysis of the Oxygen Evolution Reaction.

A comprehensive study of the synergy between Fe and six transition metals (M=Ti, Co, Ni, Cu, Ag, Au), and how their M-Fe oxides electrocatalyze the oxygen evolution reaction (OER) was undertaken. Measurements were made using metal disks as the working electrodes and the addition of Fe3+ ions to the 1 m KOH electrolyte. The surfaces of the metal disks were oxidized after the OER. Interestingly, Fe interacted synergistically with all metal oxide layers except for that of Ti, resulting in enhanced catalytic activity for the OER. At an overpotential (η) of 400 mV, the current densities of the Ni and Ag disks in the Fe3+ ions-spiked electrolyte increased by 253 and 132 times, respectively, whereas it was only 20-30 times for the Co and Cu disks (compared with the OER in pure KOH at η=400 mV). The Tafel slopes of the Fe, Co, Ni, Cu, and Ag disks in 1 m KOH+Fe3+ electrolyte were in the range of 29-42 mV dec-1 . The surface morphology and post-OER concentration of Fe in the catalysts could not be used to account for differences in the OER activities. Cyclic voltammetry showed that improvements in the OER performance were accompanied by changes in the redox features of the metal disk electrodes, which indicated the presence of electronic interactions between them and the Fe3+ . Strikingly, this was not observed between Ti and the Fe3+ ions, which could explain the lack of synergy between Ti and Fe3+ towards the OER catalysis. Electrochemical impedance spectroscopy indicated that the charge-transfer resistances of all the electrodes (except Ti) decreased after the addition of Fe3+ ions. Fe plays an important role in all these observed phenomena and we propose that the surface-adsorbed Fe species serve as the main active sites for OER in these synergistic M-Fe combinations.

On the Role of Sulfur for the Selective Electrochemical Reduction of CO2 to Formate on CuS x Catalysts.

The efficient electroreduction of CO2 has received significant attention as it is one of the crucial means to develop a closed-loop anthropogenic carbon cycle. Here, we describe the mechanistic workings of an electrochemically deposited CuS x catalyst that can reduce CO2 to formate with a Faradaic efficiency (FEHCOO-) of 75% and geometric current density ( jHCOO-) of -9.0 mA/cm2 at -0.9 V versus the reversible hydrogen electrode. At this potential, the formation of other CO2 reduction products such as hydrocarbons and CO was notably suppressed (total FE < 4%). The formate intermediate (HCOO*) was identified by operando Raman spectroscopy with isotopic labeling. A combination of electrochemical and materials characterization techniques revealed that the high selectivity toward formate production can be attributed to the effect of S dopants on the Cu catalyst, rather than surface morphology. Density functional theory calculations showed that the presence of sulfur weakens the HCOO* and *COOH adsorption energies, such that the formation of *COOH toward CO is suppressed, while the formation of HCOO* toward formate is favored.

Effects of Electrolyte Anions on the Reduction of Carbon Dioxide to Ethylene and Ethanol on Copper (100) and (111) Surfaces.

The CO2 electroreduction reaction has been investigated on Cu(100) and Cu(111) surfaces in 0.1 m aqueous solutions of KClO4 , KCl, KBr, and KI electrolyte. The formation of ethylene and ethanol on these surfaces generally increased as the electrolyte anion was changed from ClO4- →Cl- →Br- →I- . For example, on Cu(100) at -1.23 V versus RHE, as the electrolyte anion changed from ClO4- to I- , the faradaic efficiency (FE) of ethylene formation increased from 31 to 50 %, FEethanol increased from 7 to 16 %, and the associated current densities increased five- and sevenfold, respectively. A remarkable total FE of up to 74 % for C2 and C3 products was obtained in the presence of KI. Despite surface roughening in the presence of the electrolytes, the Cu(100) electrode still enhanced the formation of C2 compounds better than Cu(111). The favorable reduction of CO2 to C2 products in KI electrolyte was correlated with a higher *CO population on the surface, as shown using linear sweep voltammetry. In situ Raman spectroscopy indicated that the coordination environment of *CO was altered by the used electrolyte anion. Thus, apart from affecting the morphology of the electrode and local pH value, we propose that the anion plays a critical role in enhancing the formation of C2 products by tuning the coordination environment of adsorbed *CO, which gives rise to more efficient C-C coupling.

The effects of currents and potentials on the selectivities of copper toward carbon dioxide electroreduction.

Copper electrodes have been shown to be selective toward the electroreduction of carbon dioxide to ethylene, carbon monoxide, or formate. However, the underlying causes of their activities, which have been attributed to a rise in local pH near the surface of the electrode, presence of atomic-scale defects, and/or residual oxygen atoms in the catalysts, etc., have not been generally agreed on. Here, we perform a study of carbon dioxide reduction on four copper catalysts from -0.45 to -1.30 V vs. reversible hydrogen electrode. The selectivities exhibited by 20 previously reported copper catalysts are also analyzed. We demonstrate that the selectivity of carbon dioxide reduction is greatly affected by the applied potentials and currents, regardless of the starting condition of copper catalysts. This study shows that optimization of the current densities at the appropriate potential windows is critical for designing highly selective copper catalysts.

Ruthenium-Tungsten Composite Catalyst for the Efficient and Contamination-Resistant Electrochemical Evolution of Hydrogen.

A new catalyst, prepared by a simple physical mixing of ruthenium (Ru) and tungsten (W) powders, has been discovered to interact synergistically to enhance the electrochemical hydrogen evolution reaction (HER). In an aqueous 0.5 M H2SO4 electrolyte, this catalyst, which contained a miniscule loading of 2-5 nm sized Ru nanoparticles (5.6 µg Ru per cm2 of geometric surface area of the working electrode), required an overpotential of only 85 mV to drive 10 mA/cm2 of H2 evolution. Interestingly, our catalyst also exhibited good immunity against deactivation during HER from ionic contaminants, such as Cu2+ (over 24 h). We unravel the mechanism of synergy between W and Ru for catalyzing H2 evolution using Cu underpotential deposition, photoelectron spectroscopy, and density functional theory (DFT) calculations. We found a decrease in the d-band and an increase in the electron work function of Ru in the mixed composite, which made it bind to H more weakly (more Pt-like). The H-adsorption energy on Ru deposited on W was found, by DFT, to be very close to that of Pt(111), explaining the improved HER activity.

Investigating the Role of Copper Oxide in Electrochemical CO2 Reduction in Real Time.

Copper oxides have been of considerable interest as electrocatalysts for CO2 reduction (CO2R) in aqueous electrolytes. However, their role as an active catalyst in reducing the required overpotential and improving the selectivity of reaction compared with that of polycrystalline copper remains controversial. Here, we introduce the use of selected-ion flow tube mass spectrometry, in concert with chronopotentiometry, in situ Raman spectroscopy, and computational modeling, to investigate CO2R on Cu2O nanoneedles, Cu2O nanocrystals, and Cu2O nanoparticles. We show experimentally that the selective formation of gaseous C2 products (i.e., ethylene) in CO2R is preceded by the reduction of the copper oxide (Cu2OR) surface to metallic copper. On the basis of density functional theory modeling, CO2R products are not formed as long as Cu2O is present at the surface because Cu2OR is kinetically and energetically more favorable than CO2R.

Rational Design of Sulfur-Doped Copper Catalysts for the Selective Electroreduction of Carbon Dioxide to Formate.

The selective electroreduction of CO2 to formate (or formic acid) is of great interest in the field of renewable-energy utilization. In this work, we designed a sulfur-doped Cu2 O-derived Cu catalyst and showed that the presence of sulfur can tune the selectivity of Cu significantly from the production of various CO2 reduction products to almost exclusively formate. Sulfur is doped into the Cu catalysts by dipping the Cu substrates into ammonium polysulfide solutions. Catalyst films with the highest sulfur content of 2.7 at % showed the largest formate current density (jHCOO- ) of -13.9 mA cm-2 at -0.9 V versus the reversible hydrogen electrode (RHE), which is approximately 46 times larger than that previously reported for Cu(110) surfaces. At -0.8 V versus RHE, the faradaic efficiency of formate was maintained at approximately 75 % for 12 h of continuous electrolysis. Through the analysis of the evolution of the jHCOO- and jH2 values with the sulfur content, we show that sulfur doping increases formate production and suppresses the hydrogen evolution reaction. Ag-S and Cu-Se catalysts did not exhibit any significant enhancement towards the reduction of CO2 to formate. This demonstrates clearly that sulfur and copper acted synergistically to promote the selective formation of formate. A hypothesis about the role of sulfur is proposed and discussed.

Interface confined hydrogen evolution reaction in zero valent metal nanoparticles-intercalated molybdenum disulfide.

Interface confined reactions, which can modulate the bonding of reactants with catalytic centres and influence the rate of the mass transport from bulk solution, have emerged as a viable strategy for achieving highly stable and selective catalysis. Here we demonstrate that 1T'-enriched lithiated molybdenum disulfide is a highly powerful reducing agent, which can be exploited for the in-situ reduction of metal ions within the inner planes of lithiated molybdenum disulfide to form a zero valent metal-intercalated molybdenum disulfide. The confinement of platinum nanoparticles within the molybdenum disulfide layered structure leads to enhanced hydrogen evolution reaction activity and stability compared to catalysts dispersed on carbon support. In particular, the inner platinum surface is accessible to charged species like proton and metal ions, while blocking poisoning by larger sized pollutants or neutral molecules. This points a way forward for using bulk intercalated compounds for energy related applications.