skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Circumventing the scaling relationship on bimetallic monolayer electrocatalysts for selective CO 2 reduction
Electrochemical conversion of CO 2 into value-added chemicals continues to draw interest in renewable energy applications. Although many metal catalysts are active in the CO 2 reduction reaction (CO 2 RR), their reactivity and selectivity are nonetheless hindered by the competing hydrogen evolution reaction (HER). The competition of the HER and CO 2 RR stems from the energy scaling relationship between their reaction intermediates. Herein, we predict that bimetallic monolayer electrocatalysts (BMEs) – a monolayer of transition metals on top of extended metal substrates – could produce dual-functional active sites that circumvent the scaling relationship between the adsorption energies of HER and CO 2 RR intermediates. The antibonding interaction between the adsorbed H and the metal substrate is revealed to be responsible for circumventing the scaling relationship. Based on extensive density functional theory (DFT) calculations, we identify 11 BMEs which are highly active and selective toward the formation of formic acid with a much suppressed HER. The H–substrate antibonding interaction also leads to superior CO 2 RR performance on monolayer-coated penta-twinned nanowires.  more » « less
Award ID(s):
1828019
PAR ID:
10330453
Author(s) / Creator(s):
;
Date Published:
Journal Name:
Chemical Science
Volume:
13
Issue:
13
ISSN:
2041-6520
Page Range / eLocation ID:
3880 to 3887
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    Electrochemical reduction of CO 2 into value-added fuels and chemicals driven by renewable energy presents a potentially sustainable route to mitigate CO 2 emissions and alleviate the dependence on fossil fuels. While tailoring the electronic structure of active components to modulate their intrinsic reactivity could tune the CO 2 reduction reaction (CO 2 RR), their use is limited by the linear scaling relation of intermediates. Due to the high susceptibility of the CO 2 RR to the local CO 2 concentration/pH and mass transportation of CO 2 /intermediates/products near the gas–solid–liquid three-phase interface, engineering catalysts’ morphological and interfacial properties holds great promise to regulate the CO 2 RR, which are irrelevant with linear scaling relation and possess high resistance to harsh reaction conditions. Herein, we provide a comprehensive overview of recent advances in tuning CO 2 reduction electrocatalysis via morphology and interface engineering. The fundamentals of the CO 2 RR and design principles for electrode materials are presented firstly. Then, approaches to build an efficient three-phase interface, tune the surface wettability, and design a favorable morphology are summarized; the relationship between the properties of engineered catalysts and their CO 2 RR performance is highlighted to reveal the activity-determining parameters and underlying catalytic mechanisms. Finally, challenges and opportunities are proposed to suggest the future design of advanced CO 2 RR electrode materials. 
    more » « less
  2. Abstract Solid‐state electrocatalysis plays a crucial role in the development of renewable energy to reshape current and future energy needs. However, finding an inexpensive and highly active catalyst to replace precious metals remains a big challenge for this technology. Here, tri‐molybdenum phosphide (Mo3P) is found as a promising nonprecious metal and earth‐abundant candidate with outstanding catalytic properties that can be used for electrocatalytic processes. The catalytic performance of Mo3P nanoparticles is tested in the hydrogen evolution reaction (HER). The results indicate an onset potential of as low as 21 mV, H2formation rate, and exchange current density of 214.7 µmol s−1g−1cat(at only 100 mV overpotential) and 279.07 µA cm−2, respectively, which are among the closest values yet observed to platinum. Combined atomic‐scale characterizations and computational studies confirm that high density of molybdenum (Mo) active sites at the surface with superior intrinsic electronic properties are mainly responsible for the remarkable HER performance. The density functional theory calculation results also confirm that the exceptional performance of Mo3P is due to neutral Gibbs free energy (ΔGH*) of the hydrogen (H) adsorption at above 1/2 monolayer (ML) coverage of the (110) surface, exceeding the performance of existing non‐noble metal catalysts for HER. 
    more » « less
  3. null (Ed.)
    Two-dimensional (2D) materials are full of surprises and fascinating potential. Motivated by a recent discovery that sub-nanometer PdMo bimetallenes can realize exceptional performance in the oxygen reduction reaction [ Nature 2019, 574 , 81–85], we explore the potential of 2D bimetallenes for catalyzing the CO 2 electroreduction reaction (CO 2 RR). Following extensive first-principles calculations on more than a hundred bimetallenes, we identify 17 Cu- and Ag-based bimetallenes, which are highly active and selective toward the formation of formic acid and simultaneously suppress the competing hydrogen evolution reaction. Equally important, we find that CO 2 RR products via intermediates of COOH and CO are disfavored on these bimetallenes. Although surface strains are developed on the bimetallenes, their contribution to the catalytic activities is moderate as compared to that of the alloying effect. This work opens the door to future applications of bimetallenes as active and selective catalysts for the CO 2 RR. 
    more » « less
  4. Abstract This work investigates the critical factors impacting electrochemical CO2reduction reaction (CO2RR) using atomically precise Au nanoclusters (NCs) as electrocatalysts. First, the influence of size on CO2RR is studied by precisely controlling NC size in the 1–2.5 nm regime. We find that the electrocatalytic CO partial current density increases for smaller NCs, but the CO Faradaic efficiency (FE) is not directly associated with the NC size. This indicates that the surface‐to‐volume ratio, i.e. the population of active sites, is the dominant factor for determining the catalytic activity, but the selectivity is not directly impacted by size. Second, we compare the CO2RR performance of Au38isomers (Au38Q and Au38T) to reveal that structural rearrangement of identical size NCs can lead to significant changes in both CO2RR activity and selectivity. Au38Q shows higher activity and selectivity towards CO than Au38T, and density functional theory (DFT) calculations reveal that the average formation energy of the key *COOH intermediate on the proposed active sites is significantly lower on Au38Q than Au38T. These results demonstrate how the structural isomerism can impact stabilization of reaction intermediates as well as the overall CO2RR performance of identical size Au NCs. Overall, this work provides important structure–property relationships for tailoring the NCs for CO2RR. 
    more » « less
  5. The electrocatalytic nitrogen reduction reaction (NRR) is of significant interest as an environmentally friendly method for NH 3 production for agricultural and clean energy applications. Selectivity of NRR vis-à-vis the hydrogen evolution reaction (HER), however, is thought to adversely impact many potential catalysts, including Earth-abundant transition metal oxynitrides. Relative HER/NRR selectivities are therefore directly compared for two transition metal oxynitrides with different metal oxophilicities—Co and V. Electrocatalytic current–potential measurements, operando fluorescence, absorption, and GC measurements of H 2 and NH 3 production, ex situ X-ray photoelectron spectroscopy (XPS), and density functional theory (DFT) calculations are combined to directly compare NRR and HER activities under identical reaction conditions. Results show that cobalt oxynitrides – with Co primarily in the Co( ii ) oxidation state – are NRR active at pH 10, with electrochemical reduction of both lattice nitrogen and dissolved N 2 , the latter occurring without N incorporation into the lattice. Removal of lattice N then yields Co( ii ) oxide, which is still NRR active. These results are complemented by calculations showing that N 2 binding at Co( ii ) sites is energetically favored over binding at Co( iii ) sites. GC analysis demonstrates that H 2 production occurs in concert with ammonia production but at a far greater rate. In contrast, vanadium oxynitride films are HER inactive under the same (pH 10) conditions, as well as at pH 7, but are NRR active at pH 7. DFT calculations indicate that a major difference in the two materials is hindered O–H dissociation of H 2 O adsorbed at O-ligated Co vs. V cation centers. The combined studies indicate significant variation in HER vs. NRR selectivity as a function of employed transition metal oxynitrides, as well as different HER mechanisms in V and Co oxynitrides. 
    more » « less