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Electrolysis of bicarbonate-containing CO capture solutions is a promising approach towards achieving low-cost carbon-neutral chemicals production. However, the parasitic bicarbonate-mediated hydrogen evolution reaction (HER) and electrode instability in the presence of trace impurities remain major obstacles to overcome. This work demonstrates that the combined use of titanium dioxide (TiO) overlayers with the chelating agent ethylene diamine tetra-acetic acid (EDTA) significantly enhances the selectivity and stability of Ag-based electrocatalysts for bicarbonate electrolysis. The amorphous TiO overlayers suppress the HER by over 50 % at potentials more negative than -0.7 V vs. RHE, increasing the CO faradaic efficiency (FE) by 33 % (relative). In situ surface-enhanced Raman spectroscopy (SERS) measurements reveal the absence of near-surface bicarbonate species and an abundance of CO reduction intermediates at the Ag|TiO buried interface, suggesting that the overlayers suppress HER by blocking bicarbonate ions from reaching the buried active sites. In accelerated degradation tests with 5 ppm of Fe(III) impurity, the addition of EDTA allows stable CO production with >47 % FE, while the electrodes rapidly deactivate in the absence of EDTA. This work highlights the use of TiO overlayers for enhancing the CO : H ratio while simultaneously protecting electrocatalysts from impurities likely to be present in "open" carbon capture systems.
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http://dx.doi.org/10.1002/anie.202404758 | DOI Listing |
ACS Appl Mater Interfaces
September 2025
Department of Chemical Engineering, Columbia Electrochemical Engineering Center, Lenfest Center for Sustainable Energy Columbia University in the City of New York, New York, New York 10027, United States.
Molecular catalysts, such as metalated porphyrins, are attractive cocatalysts for photocatalytic water splitting owing to their potential to simultaneously catalyze target reactions at their metal center, extend charge-separated-state lifetimes, and accumulate the requisite charge for product formation. However, porphyrin catalysts, like most molecular catalysts, are often limited by poor stability associated with demetalation, inactivation by undesired bonding (e.g.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Department of Energy Engineering/KENTECH Institute for Environmental and Climate Technology, Korea Institute of Energy Technology (KENTECH), Naju, Jeollanam-do, 58330, Republic of Korea.
Surface and interface engineering is essential for constructing efficient and stable photoelectrodes for photoelectrochemical (PEC) solar fuel production. Despite the recent advances in photoelectrode optimization for the practical application, the corresponding interfacial reaction mechanism has not been elucidated owing to a lack of suitable measurements at the semiconductor-electrolyte interface (SEI). Herein, the key factor for an interfacial reaction in a model system (WO photoanode coated with amorphous TiO overlayers) is elucidated using operando spectroelectrochemistry.
View Article and Find Full Text PDFLangmuir
August 2025
International Research Centre for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi'an Jiaotong University, Xi'an 710049, Shaanxi, China.
Hematite (α-FeO) represents a photoelectrode material that holds high potential to realize efficient and stable photoelectrochemical (PEC) hydrogen production due to its narrow bandgap for efficient solar absorption and good stability in alkaline electrolytes. However, pure α-FeO has been plagued by its poor conductivity with low carrier mobility and rapid charge recombination, which greatly hinder its photoelectrochemical applications. Herein, a hybrid photoanode is rationally designed by growing an amorphous TiO overlayer on a Ti-doped α-FeO nanorod photoanode to passivate surface states for improved PEC performance.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry, The University of Texas at Austin, Austin, Texas 78712, United States.
The properties of semiconductor|liquid interfaces play a critical role in determining the efficiency of solar-to-hydrogen (STH) conversion. Here, we investigate how molecular functionalization of Si(111) and Si(111)|TiO surfaces impacts photoelectrochemical (PEC) hydrogen production efficiency. We find that functionalization of ∼3% of the atop sites of Si(111) with either 9-anthracene (Anth) or 5-tetracene (Tet), with the remaining sites passivated by methyl groups, provides substrates with high electronic quality and low surface oxide densities, as determined by X-ray photoelectron spectroscopy (XPS) measurements.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Institut de Chimie Physique, Université Paris-Saclay, CNRS UMR 8000, Orsay, F-91405, France.
Strong Metal-Support Interaction (SMSI) is a key concept in heterogeneous catalysis, but it remains underexplored in the context of photon-to-hydrogen conversion, as coupling of metallic nanoparticles with photocatalysts is overlooked and only discussed in terms of Schottky barrier formation. In this study, we provide deep insights into the effect of Au encapsulation with TiO overlayer on enhancing photocatalytic hydrogen generation. Our findings reveal that the construction of a SMSI-like nanostructure induces the formation of oxygen vacancies at the Au‒TiO interface which actively facilitate charge carrier separation through interfacial band reconstruction.
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