To date, copper is the only heterogeneous catalyst that has shown a propensity to produce valuable hydrocarbons and alcohols, such as ethylene and ethanol, from electrochemical CO2 reduction (CO2R). There are variety of factors that impact CO2R activity and selectivity, including the catalyst surface structure, morphology, composition, the choice of electrolyte ions and pH, and the electrochemical cell design. Many of these factors are often intertwined, which can complicate catalyst discovery and design efforts. Here we take a broad and historical view of these different aspects and their complex interplay in CO2R catalysis on Cu, with the purpose of providing new insights, critical evaluations, and guidance to the field with regard to research directions and best practices. First, we describe the various experimental probes and complementary theoretical methods that have been used to discern the mechanisms by which products are formed, and next we present our current understanding of the complex reaction networks for CO2R on Cu. We then analyze two key methods that have been used in attempts to alter the activity and selectivity of Cu: nanostructuring and the formation of bimetallic electrodes. Finally, we offer some perspectives on the future outlook for electrochemical CO2R.

/pdf/progress-and-perspectives-of-electrochemical-co2-reduction-hut0der0e7.pdf

Progress and Perspectives of Electrochemical CO2 Reduction on Copper in Aqueous Electrolyte

The production of sustainable hydrogen with water electrolyzers is envisaged as one of the most promising ways to match the continuously growing demand for renewable electricity storage. While so far regarded as fast when compared to the oxygen evolution reaction (OER), the hydrogen evolution reaction (HER) regained interest in the last few years owing to its poor kinetics in alkaline electrolytes. Indeed, this slow kinetics not only may hinder the foreseen development of the anionic exchange membrane water electrolyzer (AEMWE), but also raises fundamental questions regarding the parameters governing the reaction. In this perspective, we first briefly review the fundamentals of the HER, emphasizing how studies performed on model electrodes allowed for achieving a good understanding of its mechanism under acidic conditions. Then, we discuss how the use of physical descriptors capturing the sole properties of the catalyst is not sufficient to describe the HER kinetics under alkaline conditions, thus forcing the catalysis community to adopt a more complex picture taking into account the electrolyte structure at the electrochemical interface. This work also outlines new techniques, such as spectroscopies, molecular simulations, or chemical approaches that could be employed to tackle these new fundamental challenges, and potentially guide the future design of practical and cheap catalysts while also being useful to a wider community dealing with electrochemical energy storage devices using aqueous electrolytes.

/pdf/the-hydrogen-evolution-reaction-from-material-to-interfacial-2vw1w6pisr.pdf

The hydrogen evolution reaction: from material to interfacial descriptors

Electrochemical and photoelectrochemical CO2 reduction technologies offer the promise of zero-carbon-emission renewable fuels needed for heavy-duty transportation. However, the inert nature of the CO2 molecule poses a fundamental challenge that must be overcome before efficient (photo)electrochemical CO2 reduction at scale will be achieved. Optimal catalysts exhibit enduring stability, fast kinetics, high selectivity, and low manufacturing cost. Identifying catalytic mechanisms of CO2 reduction in (photo)electrochemical systems could accelerate design of efficient catalysts. In recent decades, numerous theoretical studies have contributed to our understanding of CO2 reduction pathways and identifying rate-limiting steps. Although a significant body of work exists regarding homogeneous electrocatalysis for CO2 reduction, this review focuses specifically on the theory of heterogeneous (photo)electrochemical reduction. We first give an overview of the relevant thermodynamics and semiconductor physics. We the...

Theoretical Insights into Heterogeneous (Photo)electrochemical CO2 Reduction

The electrochemical method of combining N2 and H2 O to produce ammonia (i.e., the electrochemical nitrogen reduction reaction [E-NRR]) continues to draw attention as it is both environmentally friendly and well suited for a progressively distributed farm economy. Despite the multitude of recent works on the E-NRR, further progress in this field faces a bottleneck. On the one hand, despite the extensive exploration and trial-and-error evaluation of E-NRR catalysts, no study has stood out to become the stage protagonist. On the other hand, the current level of ammonia production (microgram-scale) is an almost insurmountable obstacle for its qualitative and quantitative determination, hindering the discrimination between true activity and contamination. Herein i) the popular theory and mechanism of the NRR are introduced; ii) a comprehensive summary of the recent progress in the field of the E-NRR and related catalysts is provided; iii) the operational procedures of the E-NRR are addressed, including the acquisition of key metrics, the challenges faced, and the most suitable solutions; iv) the guiding principles and standardized recommendations for the E-NRR are emphasized and future research directions and prospects are provided.

Comprehensive Understanding of the Thriving Ambient Electrochemical Nitrogen Reduction Reaction.

We present a new open repository for chemical reactions on catalytic surfaces, available at https://www.catalysis-hub.org
 . The featured database for surface reactions contains more than 100,000 chemisorption and reaction energies obtained from electronic structure calculations, and is continuously being updated with new datasets. In addition to providing quantum-mechanical results for a broad range of reactions and surfaces from different publications, the database features a systematic, large-scale study of chemical adsorption and hydrogenation on bimetallic alloy surfaces. The database contains reaction specific information, such as the surface composition and reaction energy for each reaction, as well as the surface geometries and calculational parameters, essential for data reproducibility. By providing direct access via the web-interface as well as a Python API, we seek to accelerate the discovery of catalytic materials for sustainable energy applications by enabling researchers to efficiently use the data as a basis for new calculations and model generation.

/pdf/catalysis-hub-org-an-open-electronic-structure-database-for-5guauq2cvz.pdf

Catalysis-Hub.org, an open electronic structure database for surface reactions.

Identifying efficient electrocatalysts with low overpotential and high selectivity for producing ammonia from nitrogen gas is essential for any future electrocatalytic nitrogen reduction reaction (...

Prediction of Highly Selective Electrocatalytic Nitrogen Reduction at Low Overpotential on a Mo-Doped g-GaN Monolayer

A detailed atomic-scale description of the electrochemical interface is essential to the understanding of electrochemical energy transformations. In this work, we investigate the charge of solvated protons at the Pt(111) | H2O and Al(111) | H2O interfaces. Using semi-local density-functional theory as well as hybrid functionals and embedded correlated wavefunction methods as higher-level benchmarks, we show that the effective charge of a solvated proton in the electrochemical double layer or outer Helmholtz plane at all levels of theory is fractional, when the solvated proton and solvent band edges are aligned correctly with the Fermi level of the metal (EF). The observed fractional charge in the absence of frontier band misalignment arises from a significant overlap between the proton and the electron density from the metal surface, and results in an energetic difference between protons in bulk solution and those in the outer Helmholtz plane.

/pdf/understanding-the-apparent-fractional-charge-of-protons-in-3499btw1wi.pdf

Understanding the apparent fractional charge of protons in the aqueous electrochemical double layer.

Understanding the apparent fractional charge of protons in the aqueous electrochemical double layer

We present a cyclic process for selective and anisotropic atomic layer etching of copper: an oxygen plasma modulates the depth and directionality of the oxidized layer, while formic acid vapor sele...

Precise Control of Nanoscale Cu Etching via Gas-Phase Oxidation and Chemical Complexation

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Papers

Prediction of Highly Selective Electrocatalytic Nitrogen Reduction at Low Overpotential on a Mo-Doped g-GaN Monolayer

Understanding the apparent fractional charge of protons in the aqueous electrochemical double layer.

Understanding the apparent fractional charge of protons in the aqueous electrochemical double layer

Precise Control of Nanoscale Cu Etching via Gas-Phase Oxidation and Chemical Complexation