Establishing Non‐stoichiometric Ti4O7 Assisted Asymmetrical C‐C Coupling for Highly Energy‐Efficient Electroreduction of Carbon Monoxide DOI Open Access

Xuli Hu,

Junchen Xu,

Yuan Gao

et al.

Angewandte Chemie, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 22, 2024

Abstract Exploring an appropriate support material for Cu‐based electrocatalyst is conducive stably producing multi‐carbon chemicals from electroreduction of carbon monoxide. However, the insufficient metal‐support adaptability and low conductivity would hinder C−C coupling capacity energy efficiency. Herein, non‐stoichiometric Ti 4 O 7 was incorporated into Cu electrocatalysts (Cu−Ti ), served as a highly conductive stable energy‐efficient electrochemical conversion CO. The abundant oxygen vacancies originated ordered lattice defects in facilitate water dissociation CO adsorption to accelerate hydrogenation *COH. adaptable interface Cu−Ti enables direct asymmetrical between *CO on *COH , which significantly lowers reaction barrier C 2+ products formation. Additionally, excellent electroconductivity benefits charge transfer through robust Cu/Ti minimizing loss. Thus, optimized 20Cu−Ti catalyst exhibits impressive selectivity 96.4 % ultrahigh efficiency 45.1 products, along with remarkable partial current density 432.6 mA cm −2 . Our study underscores novel strategy material, advancing development Cu‐supported catalysts efficient

Language: Английский

Recent research progress of bismuth-based electrocatalysts for electrochemical reduction of carbon dioxide DOI Open Access
Chen Zhang, Fei Liu, Jiajun Wang

et al.

Microstructures, Journal Year: 2025, Volume and Issue: 5(1)

Published: Feb. 18, 2025

With modern science and technology developing, the concentration of atmospheric carbon oxide (CO2) has increased substantially. CO2 electroreduction reaction (CO2RR) can efficiently utilize sustainable power to produce value-added chemicals implement energy storage. Previous researches have proved bismuth metal bismuth-based materials transfer formate selectively. However, in this paper, latest progress synthesis advanced electrocatalysts with CO2RR catalysts is reviewed from aspects catalyst material design, synthesis, mechanism performance verification/optimization. Some methods designing are discussed analyzed different angles, including morphology, defects heterogeneous structures. In particular, application situ characterization technique introduced. Subsequently, some views expectations regarding current challenges future potential research presented.

Language: Английский

Citations

1

Stable Cu+/Cu2+ species derived from in-situ growing Cu-S-V bonds in CuVxS electrocatalysts enables high efficiency CO2 electroreduction to methanol DOI

Xuli Hu,

Zhen Zhang,

Zhenyao Li

et al.

Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 358, P. 124445 - 124445

Published: July 25, 2024

Language: Английский

Citations

4

Boosting electrochemical CO2 reduction by strong electronic interaction at the interface of Bi/SnO2 heterostructures DOI
Zeyu Wang,

Yaling Jia,

Shangqing Zhao

et al.

Journal of Colloid and Interface Science, Journal Year: 2025, Volume and Issue: unknown, P. 137528 - 137528

Published: April 1, 2025

Language: Английский

Citations

0

Controlled SnO2 Nanostructures for Enhanced Sensing of Hydrogen Sulfide and Nitrogen Dioxide DOI Creative Commons
Youssef Doubi, Bouchaib Hartiti, Abdelkrim Batan

et al.

Sensors and Actuators B Chemical, Journal Year: 2025, Volume and Issue: 440, P. 137878 - 137878

Published: April 28, 2025

Language: Английский

Citations

0

In Situ/Operando Characterization Techniques for Reaction Interface in Electrocatalytic CO2 Reduction DOI

Zezhong Xie,

Y L Liu,

Lanqi He

et al.

Small, Journal Year: 2025, Volume and Issue: unknown

Published: May 2, 2025

Abstract CO 2 reduction reaction (CO RR) has attracted considerable attention as a sustainable approach for carbon capture and conversion. However, the dynamic nature of electrocatalysts under operational conditions, particularly at interface, presents significant challenges understanding mechanisms optimizing catalyst design. In situ/operando characterization techniques are crucial to interfaces RR. This review focuses on various in employed explore interfaces, insights derived from these studies, their implications

Language: Английский

Citations

0

Visualizing Electrochemical CO2 Reduction Reaction: Recent Progress of In Situ Liquid Cell Transmission Electron Microscopy DOI

Zeyu Guo,

Paul Paciok,

Robert Zandonella

et al.

Advanced Functional Materials, Journal Year: 2025, Volume and Issue: unknown

Published: May 7, 2025

Abstract The electrochemical carbon dioxide reduction reaction (CO 2 RR), driven by renewable energy, represents a promising approach for converting CO into valuable fuels and chemicals, addressing pressing energy environmental challenges. However, the development of high‐performance RR electrocatalysts remains constrained limited understanding their dynamic evolution mechanisms, intrinsic stability factors, activity origins under operational conditions. Transmission electron microscopy (TEM), with its unparalleled spatial resolution at nanoscale atomic level, combined microregional analytical capabilities, has become vital tool investigating heterogeneous electrocatalysis. Among these techniques, in situ liquid cell TEM (LC‐TEM) enables real‐time visualization structural morphological changes catalysts during RR. This review critically examines recent advancements LC‐TEM applications RR, focusing on three key aspects electrocatalysts: morphology, transformation phase structure, identification active sites. It highlights pivotal role elucidating structure–activity relationships activation deactivation mechanisms electrocatalysts. Moreover, discusses primary challenges facing outlines future directions advancing electrolysis research.

Language: Английский

Citations

0

Interfacial Engineering of In-SnO2 Heterostructure for Promoting Electrocatalytic CO2 Reduction to Formate DOI

Ling-Ling Zhou,

Zhenping Qu, Liang Fu

et al.

Applied Catalysis B Environment and Energy, Journal Year: 2025, Volume and Issue: unknown, P. 125471 - 125471

Published: May 1, 2025

Language: Английский

Citations

0

Mono‐/Bimetallic Doped and Heterostructure Engineering for Electrochemical Energy Applications DOI Creative Commons
Dawei Chu,

Zhongwang Liang,

Yi Cheng

et al.

ChemSusChem, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 25, 2024

Abstract Designing efficient materials is crucial to meeting specific requirements in various electrochemical energy applications. Mono‐/bimetallic doped and heterostructure engineering have attracted considerable research interest due their unique functionalities potential for conversion storage. However, addressing material imperfections such as low conductivity poor active sites requires a strategic approach design. This review explores the latest advancements modified by mono‐/bimetallic heterojunction strategies It can be subdivided into three key points: (i) regulatory mechanisms of metal doping materials; (ii) preparation methods with strategies; (iii) synergistic effects two approaches, further highlighting applications supercapacitors, alkaline ion batteries, electrocatalysis. Finally, concludes perspectives recommendations advance these technologies.

Language: Английский

Citations

2

Heterogeneous Electrochemical Carbon Dioxide Reduction in Aqueous Medium Using a Novel N4‐Macrocyclic Cobalt Complex DOI Creative Commons
Libo Sun, Tan Su,

Adrian C. Fisher

et al.

Small Methods, Journal Year: 2024, Volume and Issue: 8(11)

Published: Aug. 11, 2024

Abstract Molecular catalysts represent an exceptional class of materials in the realm electrochemical carbon dioxide reduction (CO 2 RR), offering distinct advantages owing to their adaptable structure, which enables precise control electronic configurations and outstanding performance CO RR. This study introduces innovative approach heterogeneous RR aqueous environment, utilizing a newly synthesized N4‐macrocyclic cobalt complex generated through dimerization coupling reaction. By incorporating quaterpyridine moiety, this exhibits capability catalyze at low overpotentials reaches near‐unity production across wide potential range, as verified by online mass spectrometry situ attenuated total reflectance‐Fourier transform infrared spectroscopy. Comprehensive computational models demonstrate superiority quarterpyridine moiety mediating conversion compared counterpart. work not only propels field but also underscores promising complexes featuring moieties advancing sustainable technologies within environments.

Language: Английский

Citations

1

Establishing Non‐stoichiometric Ti4O7 Assisted Asymmetrical C‐C Coupling for Highly Energy‐Efficient Electroreduction of Carbon Monoxide DOI

Xuli Hu,

Junchen Xu,

Yi Gao

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 22, 2024

Abstract Exploring an appropriate support material for Cu‐based electrocatalyst is conducive stably producing multi‐carbon chemicals from electroreduction of carbon monoxide. However, the insufficient metal‐support adaptability and low conductivity would hinder C−C coupling capacity energy efficiency. Herein, non‐stoichiometric Ti 4 O 7 was incorporated into Cu electrocatalysts (Cu−Ti ), served as a highly conductive stable energy‐efficient electrochemical conversion CO. The abundant oxygen vacancies originated ordered lattice defects in facilitate water dissociation CO adsorption to accelerate hydrogenation *COH. adaptable interface Cu−Ti enables direct asymmetrical between *CO on *COH , which significantly lowers reaction barrier C 2+ products formation. Additionally, excellent electroconductivity benefits charge transfer through robust Cu/Ti minimizing loss. Thus, optimized 20Cu−Ti catalyst exhibits impressive selectivity 96.4 % ultrahigh efficiency 45.1 products, along with remarkable partial current density 432.6 mA cm −2 . Our study underscores novel strategy material, advancing development Cu‐supported catalysts efficient

Language: Английский

Citations

1