arXiv subjects

Alexis T. Bell

Publications and source records attributed to Alexis T. Bell.

4 recordsLinked to original sources

arXiv2025

Membrane-Electrode Assemblies for Electrochemical Reduction of CO2 to Ethylene: Design for Minimal Energy Consumption

Membrane-electrode-assembly (MEA) cells with copper (Cu) cathodes show strong potential for electrochemical CO2 reduction to ethylene (C2H4), but achieving high C2H4 selectivity remains a challenge due to competing hydrogen evolution. This selectivity is highly sensitive to the local microenvironment near the Cu catalyst surface. In this study, a 1-D, multiphysics continuum model is utilized to investigate how MEA cell performance and faradaic efficiency (FE) to C2H4 are affected by both component properties and operating conditions, with particular focus on coupled transport and reaction phenomena. Key parameters include cathode electrochemically active surface area (ECSA) and catalyst layer thickness. Halving catalyst layer thickness increases FE to C2H4 by 2% and lowers the cell voltage by 40 mV. In contrast, a tenfold decrease in ECSA results increases the FE to C2H4 by 7% but leads increase cell voltage at a given current density by 150 mV. This tradeoff occurs because the potential distribution within the cathode catalyst layer is the primary driving force for C2H4 formation. Increased cell voltage also raises the energy cost of C2H4 production. This model framework enables techno-economic assessments and identifies key factors that must be optimized to enable economically viable production of C2H4 via electrochemical reduction of CO2.

physics.chem-ph↗

arXiv2024

Operando probing of nanocracking in CuO-derived Cu during CO$_2$ electroreduction

Identifying and controlling active sites in electrocatalysis remains a grand challenge due to restructuring of catalysts in the complex chemical environments during operation. Inactive precatalysts can transform into active catalysts under reaction conditions, such as oxide-derived Cu (OD-Cu) for CO$_2$ electroreduction displaying improved production of multicarbon (C$_{2+}$) chemicals. Revealing the mechanism of active site origin in OD-Cu catalysts requires in situ/operando characterizations of structure, morphology, and valence state evolution with high spatial and temporal resolution. Applying newly developed electrochemical liquid cell transmission electron microscopy combined with X-ray absorption spectroscopy, our multimodal operando techniques unveil the formation pathways of OD-Cu active sites from CuO bicrystal nanowire precatalysts. Rapid reduction of CuO directly to Cu within 60 seconds generates a nanocrack network throughout the nanowire, via formation of "boundary nanocracks" along the twin boundary and "transverse nanocracks" propagating from the surface to the center of the nanowire. The nanocrack network further reconstructs, leading to a highly porous structure rich in Cu nanograins, with a boosted specific surface area and density of active sites for C$_{2+}$ products. These findings suggest a means to optimize active OD-Cu nanostructures through nanocracking by tailoring grain boundaries in CuO precatalysts. More generally, our advanced operando approach opens new opportunities for mechanistic insights to enable improved control of catalyst structure and performance.

cond-mat.mtrl-sci↗

arXiv2020

The Critical Role of Thermal Fluctuations for Electrocatalytic Metal Surface Properties and CO Binding Trends

This work addresses a longstanding theoretical discrepancy using Density Functional Theory (DFT) with experimental observations of CO binding trends on electrocatalytically relevant metals for the CO2 reduction reaction (CO2RR). By introducing thermal fluctuations using appropriate statistical mechanical NVT and NPT ensembles, we show that DFT with universal dispersion interactions yields qualitatively better metal surface strain trends and CO binding energetics, consistently predicts the correct site preference for all metals due to thermally induced surface distortions that preferentially exposes the undercoordinated atop site for Cu(111) and Pt(111), and for the weak binding Ag(111) and Au(111) surfaces at finite temperatures shows CO-metal interactions that are a mixture of chemisorbed and physisorbed species. This study better places theory as an equal partner to experimental heterogeneous catalysis by demonstrating the need to fully account for finite temperature fluctuations to make contact with surface science experiments.

physics.chem-ph↗

arXiv2018

Reaction Mechanism of the Selective Reduction of CO$_2$ to CO by a Tetraaza [Co$^\text{II}$N$_4$H]$^{2+}$ Complex in the Presence of Protons

The tetraaza [Co$^\text{II}$N$_4$H]$^{2+}$ complex (\textbf{1}) is remarkable for its ability to selectively reduce CO$_2$ to CO with 45\% Faradaic efficiency and a CO to H$_2$ ratio of 3:2. We employ density functional theory (DFT) to determine the reasons behind the unusual catalytic properties of \textbf{1} and the most likely mechanism for CO$_2$ reduction. The selectivity for CO$_2$ over proton reduction is explained by analyzing the catalyst's affinity for the possible ligands present under typical reaction conditions: acetonitrile, water, CO$_2$, and bicarbonate. After reduction of the catalyst by two electrons, formation of [Co$^\text{I}$N$_4$H]$^{+}$-CO$_{2}^{-}$ is strongly favored. Based on thermodynamic and kinetic data, we establish that the only likely route for producing CO from here consists of a protonation step to yield [Co$^\text{I}$N$_4$H]$^{+}$-CO$_{2}$H, followed by reaction with CO$_2$ to form [Co$^\text{II}$N$_4$H]$^{2+}$-CO and bicarbonate. This conclusion corroborates the idea of a direct role of CO$_2$ as a Lewis acid to assist in {C-O} bond dissociation, a conjecture put forward by other authors to explain recent experimental observations. The pathway to formic acid is predicted to be forbidden by high activation barriers, in accordance with the products that are known to be generated by \textbf{1}. Calculated physical observables such as standard reduction potentials and the turnover frequency for our proposed catalytic cycle are in agreement with available experimental data reported in the literature. The mechanism also makes a prediction that may be experimentally verified: that the rate of CO formation should increase linearly with the partial pressure of CO$_2$.

physics.chem-ph↗