Structure and Activity Comparison of Cu/CeyZr1–yOx Series Catalysts in the Reverse Water–Gas Shift Reaction DOI
Nuo Xu, Jie Ren,

Hao Lou

et al.

Energy & Fuels, Journal Year: 2024, Volume and Issue: 38(8), P. 7158 - 7166

Published: April 2, 2024

Cu-based catalysts with abundant oxygen vacancies have attracted great attention for the reverse water–gas shift (RWGS) reaction because of their enhanced activity CO2 adsorption and activation. However, effect vacancy origin on mechanism RWGS are still unclear. Herein, various Cu/CeyZr1–yOx different Ce/Zr ratios were designed used RWGS, results showed that Cu/Ce0.9Zr0.1Ox catalyst exhibited highest conversion (57.5%) 100% CO selectivity. The characterization possessed highly dispersed Cu, vacancies, optimized basic sites, synergistic three factors led to stability. Both formate carbonate pathways been confirmed Cu/CeyZr1–yOx, while dominant path is between Cu/ZrO2 Cu/CeO2.

Language: Английский

Review of Emerging Atomically Precise Composite Site‐Based Electrocatalysts DOI Open Access
Xinyi Yang,

Wanqing Song,

Tao Zhang

et al.

Advanced Energy Materials, Journal Year: 2023, Volume and Issue: 13(37)

Published: Aug. 6, 2023

Abstract Atomically precise composite site‐based catalysts with new electrocatalytic synergistic mechanisms and enhanced activities have emerged as a frontier in the electrocatalysis community. This topical review focuses on recent research advances of atomically metal sites‐based electrocatalysts. work first demonstrates an overview configurations sites, including discussion advanced methods employed for understanding sites. The then provides comprehensive organization previously reported methodologies synthesizing electrocatalysts Representative case studies are provided, starting from simple one‐step pyrolysis strategy to species‐by‐species multi‐step strategy. Based preceding discussions catalyst materials, further discusses unique raised by that different routine single species systems mainly involve oxygen reduction reaction, evolution hydrogen nitrogen carbon dioxide reaction. themes this section include true active center determination sites various types synergy mechanisms. Finally, critical unanswered questions remaining challenges, well promising underexplored directions identified.

Language: Английский

Citations

20

Synergetic bimetallic catalysts: A remarkable platform for efficient conversion of CO2 to high value-added chemicals DOI
Jundie Hu, Fengyi Yang, Jiafu Qu

et al.

Journal of Energy Chemistry, Journal Year: 2023, Volume and Issue: 87, P. 162 - 191

Published: Aug. 23, 2023

Language: Английский

Citations

19

Mesoporous TiO2 Single-Crystal Particles from Controlled Crystallization-Driven Mono-Micelle Assembly as an Efficient Photocatalyst DOI

Sixing Yin,

Lu Liu, Jialong Li

et al.

Journal of the American Chemical Society, Journal Year: 2023, Volume and Issue: 146(2), P. 1701 - 1709

Published: Dec. 29, 2023

Mesoporous materials with crystalline frameworks have been widely explored in many fields due to their unique structure and feature, but accurate manipulations over scaffolds, mainly composed of uncontrolled polymorphs, are still lacking. Herein, we a controlled crystallization-driven monomicelle assembly approach construct type uniform mesoporous TiO2 particles atomically aligned single-crystal frameworks. The resultant possess an angular shape ∼80 nm diameter, good mesoporosity (a high surface area 112 m2 g–1 mean pore size at 8.3 nm), highly oriented anatase By adjusting the evaporation rate during assembly, such facile solution-processed strategy further enables regulation particle mesopore without destruction crystallites. Such combination ordered orientation provides both effective mass charge transportation, leading significant increase hydrogen generation rate. A maximum evolution 12.5 mmol h–1 can be realized, along great stability under solar light. Our study is envisaged extend possibility single crystal growth range functional ceramics semiconductors toward advanced applications.

Language: Английский

Citations

19

A Ni-O-Ag photothermal catalyst enables 103-m 2 artificial photosynthesis with >17% solar-to-chemical energy conversion efficiency DOI Creative Commons
Yaguang Li, Fanqi Meng, Qixuan Wu

et al.

Science Advances, Journal Year: 2024, Volume and Issue: 10(20)

Published: May 17, 2024

The scalable artificial photosynthesis composed of photovoltaic electrolysis and photothermal catalysis is limited by inefficient CO 2 hydrogenation under weak sunlight irradiation. Herein, NiO nanosheets supported with Ag single atoms [two-dimensional (2D) Ni 1 0.02 O ] are synthesized for to achieve 1065 mmol g −1 hour production rate 1-sun This performance attributed the coupling effect Ag-O-Ni sites enhance weaken adsorption, resulting in 1434 yield at 300°C. Furthermore, we integrate 2D -supported reverse water-gas shift reaction commercial electrolytic water splitting construct a 103-m scale system (CO + H → ), which achieves more than 22 m 3 /day green syngas an adjustable /CO ratio (0.4-3) photochemical energy conversion efficiency >17%. research charts promising course designing practical, natural sunlight–driven systems.

Language: Английский

Citations

8

Structure and Activity Comparison of Cu/CeyZr1–yOx Series Catalysts in the Reverse Water–Gas Shift Reaction DOI
Nuo Xu, Jie Ren,

Hao Lou

et al.

Energy & Fuels, Journal Year: 2024, Volume and Issue: 38(8), P. 7158 - 7166

Published: April 2, 2024

Cu-based catalysts with abundant oxygen vacancies have attracted great attention for the reverse water–gas shift (RWGS) reaction because of their enhanced activity CO2 adsorption and activation. However, effect vacancy origin on mechanism RWGS are still unclear. Herein, various Cu/CeyZr1–yOx different Ce/Zr ratios were designed used RWGS, results showed that Cu/Ce0.9Zr0.1Ox catalyst exhibited highest conversion (57.5%) 100% CO selectivity. The characterization possessed highly dispersed Cu, vacancies, optimized basic sites, synergistic three factors led to stability. Both formate carbonate pathways been confirmed Cu/CeyZr1–yOx, while dominant path is between Cu/ZrO2 Cu/CeO2.

Language: Английский

Citations

5