Direct Observation of Electron Donation onto the Reactants and a Transient Poisoning Mechanism During CO2 Electroreduction on Ni Single Atom Catalysts
Year: 2025
Type: article
Abstract: Single atom catalysts (SACs) are an important class of materials that mediate chemical reduction reactions, a key subset of which is Ni within a carbon support for the electrochemical CO2 reduction reaction (CO2RR). However, how the metal atom/clusters and the carbon‐based support act in concert to catalyze CO2RR is not well understood, with most reports attributing activity solely to the Ni‐Nx/C moieties. To address this gap, we have undertaken a mechanistic investigation, employing in situ X‐ray absorption spectroscopy (XAS) coupled with electrochemical studies and density functional theory (DFT) calculations to further understand how Ni single atoms work in conjunction with the nitrogen‐doped carbon matrix to promote CO2RR to CO, and how the presence of impurities such as those present in CO2‐containing waste flue gases (including NOx, and CN−) changes the catalyst upon reduction. In contrast to previous works, we do not find strong evidence for a purely metal‐based reduction upon application of negative reductive potentials. Instead, we present evidence for an increase in the equatorial vs. axial splitting of Ni, consistent with electrons moving onto the reactants via the Ni single atom 3dz2 orbital. In addition, we demonstrate a transient poisoning mechanism of the Ni SAC by nitrite and thiocyanate, explaining the recovery of activity during CO2RR. These insights can aid the design of practical CO2 valorization technologies.
Source: Angewandte Chemie
Institutions: UNSW Sydney, Swinburne University of Technology, Australian National University, The University of Adelaide, Australian Nuclear Science and Technology Organisation, Australian Synchrotron, Monash University, Mark Wainwright Analytical Centre, The University of Sydney, ARC Centre of Excellence for Carbon Science and Innovation
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $5,790
Funders: Australian Nuclear Science and Technology Organisation, National Computational Infrastructure, Australian Government, Analytical Center for the Government of the Russian Federation, Australian Synchrotron, University of New South Wales, Australian Research Council, National Cancer Institute
OpenAlex ID: W4407633951