Industrial‐Level Modulation of Catalyst‐Electrolyte Microenvironment for Electrocatalytic CO2 Reduction: Challenges and Advancements DOI
Weiyi Liu,

Zunhang Lv,

Changli Wang

et al.

Advanced Energy Materials, Journal Year: 2024, Volume and Issue: unknown

Published: Sept. 9, 2024

Abstract CO 2 reduction reaction (CO RR), as a promising strategy for storing renewable energy and promoting carbon resource recycling, is critical industrial development. Previous reports have extensively explored catalyst‐electrolyte microenvironmental modulation to elucidate coupling mechanisms enhance catalytic conversion multicarbon products. Currently, most reviews mainly focus on the impact of microenvironment in low‐current systems mechanism exploration performance optimization, yet few them can integrate macroscopic applications with microscopic investigations explore relevance between development optimization. To address gap, this review focuses summarizing challenges advancements high‐current devices. By introducing models different scales sequentially, connection device clarified. Then, various invalidation effective solutions are summarized intuitively expound stability. Meanwhile, an intuitive measure rationality modulation, evaluation methods should be refined, which also covered further detail below. Finally, more valuable challenging prospects discussed guiding transformation RR.

Language: Английский

Copper-organic frameworks for electrocatalytic carbon dioxide reduction DOI
Fan Yang,

Deyu Zhu,

Chenfeng Xia

et al.

Coordination Chemistry Reviews, Journal Year: 2024, Volume and Issue: 517, P. 216021 - 216021

Published: June 19, 2024

Language: Английский

Citations

6

Strong effect-correlated electrochemical CO2 reduction DOI
Yufeng Tang,

Lin‐Bo Liu,

Mulin Yu

et al.

Chemical Society Reviews, Journal Year: 2024, Volume and Issue: 53(18), P. 9344 - 9377

Published: Jan. 1, 2024

Electrochemical CO

Language: Английский

Citations

5

Anionic Surfactant-Tuned Interfacial Water Reactivity Promoting Electrocatalytic CO2 Reduction DOI

Wangxin Ge,

Yihua Zhu, Haiyan Wang

et al.

ACS Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 18156 - 18166

Published: Nov. 23, 2024

The effects of the electrical double layer (EDL), which pertain to compositions and interactions among electrolyte species, significantly impact catalytic process. There is a pressing need investigate role components deepen our understanding EDL effects. In this study, we tune water activity within range anionic surfactants featuring different functional groups adjust H2 evolution CO2 reduction selectivity. We demonstrate that these are active in local reaction environment under cathodic potential. enhanced selectivity CO can be attributed robust interfacial hydrogen-bonding network reformed by surfactants. This diminishes dissociation promotes hydrogenation step reduction. Notably, incorporating improves performance, registering Faradaic efficiencies 89.7% (RSO3–, SDS), 97.5% (RSO4–, SLS), 98.4% (RPO42–, SMP), 98.9% (RCOO–, SL) at −1.2 V versus RHE, thereby outperforming blank KHCO3 (53.1%). research underscores crucial influence additives CO2RR.

Language: Английский

Citations

4

Isolating and stabilizing active copper species in layered double hydroxide to enhance electrocatalytic CO2 reduction to CH4 DOI

Mingzhu Yue,

Wenfu Xie, Ziyi Zhong

et al.

Journal of Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 115959 - 115959

Published: Jan. 1, 2025

Language: Английский

Citations

0

Mechanistic Insights and Advances in Electrode/Electrolyte Interfaces for Efficient Electrocatalytic CO2 Reduction to C2 Products DOI Creative Commons
Jie Chen, Yukun Xiao,

Yumin Da

et al.

SmartMat, Journal Year: 2025, Volume and Issue: 6(1)

Published: Feb. 1, 2025

ABSTRACT Electrocatalytic CO 2 reduction (ECR) is a promising approach to converting into chemicals and fuels. Among the ECR products, C products such as ethylene, ethanol, acetate have been extensively studied due their high industrial demands. However, mechanistic understanding of product formation remains unclear lack in situ or operando measurements that can observe complex instantaneous atomic evolutions adsorbates at electrode/electrolyte interface. Moreover, sensitivity reactions variations interface further widens gap between performance enhancement. To bridge this gap, first‐principle studies provide insights how influences ECR. In study, we present review investigating effects various factors interface, with an emphasis on formation. We begin by introducing essential metrics. Next, discuss classified components namely, electrocatalyst, electrolyte, adsorbates, respectively, Due interplay among these factors, aim deconvolute influence each factor clearly demonstrate impacts. Finally, outline directions for products.

Language: Английский

Citations

0

Nanoconfinement and tandem catalysis over yolk-shell catalysts towards electrochemical reduction of CO2 to multi-carbon products DOI
Lidan Sun, Xiaolin Zheng,

Yuanrui Li

et al.

Journal of Colloid and Interface Science, Journal Year: 2025, Volume and Issue: 687, P. 733 - 741

Published: Feb. 15, 2025

Language: Английский

Citations

0

Stabilization of Cu+ Sites in Cu2O-PdO Heterostructures via Orbital Engineering for Enhanced Electrochemical CO2 Reduction to Ethylene DOI

Xiaojun Wang,

Weikun Ren,

Lanlan Shi

et al.

The Journal of Physical Chemistry Letters, Journal Year: 2025, Volume and Issue: unknown, P. 3063 - 3071

Published: March 18, 2025

Electrochemical CO2 reduction to multicarbon products is vital for renewable fuels. While copper catalysts are effective C2+ production, the instability of Cu+ species hinders long-term performance. The present study reports development a Cu2O-PdO heterojunction and investigates influence an unoccupied orbital energy level regulation strategy on stabilization interfacial crystalline Cu2O during reaction (CO2RR). hybrid catalyst showed significant improvement, with 84% higher Faradaic efficiency C2H4, lasted over 7 h, vastly outperforming 2 h benchmark Cu2O. In-situ Raman, ex-situ XRD, theoretical calculations reveal that broadened d-orbital in PdO provides lower electrons, which contributes adjacent ions, high active interface significantly lowers barrier CO-CO dimerization step (2*CO → *OCCO) enhances selectivity activity CO2RR ethylene.

Language: Английский

Citations

0

Atomically dispersed cerium on copper tailors interfacial water structure for efficient CO-to-acetate electroreduction DOI Creative Commons
Peng‐Peng Yang, Zhi‐Zheng Wu,

Ye-Cheng Li

et al.

Nature Communications, Journal Year: 2025, Volume and Issue: 16(1)

Published: March 21, 2025

Electrosynthesis of acetate from carbon monoxide (CO) powered by renewable electricity offers one promising avenue to obtain valuable carbon-based products but undergoes unsatisfied selectivity because the competing hydrogen evolution reaction. We report here a cerium single atoms (Ce-SAs) modified crystalline-amorphous dual-phase copper (Cu) catalyst, in which Ce SAs reduce electron density Cu, lowering proportion interfacial K+ ion hydrated water (K·H2O) and thereby decreasing H* coverage on catalyst surface. Meanwhile, transfer Cu yields Cu+ species, boost formation active atop-adsorbed *CO (COatop), improving COatop-COatop coupling kinetics. These together lead preferential pathway ketene intermediate (*CH2-C=O) formation, then reacts with OH- enriched pulsed electrolysis generate acetate. Using this we achieve high Faradaic efficiency 71.3 ± 2.1% toward time-averaged current 110.6 2.0 mA cm−2 under mode. Furthermore, flow-cell reactor assembled can produce steadily for at least 138 hours greater than 60%. CO using faces low selectivity. Here, authors atom modulated where tailor structure, enabling highly selective CO-to-acetate conversion electrolysis.

Language: Английский

Citations

0

A Metal‐Free Boron Carbon Nitride (BCN) Photocatalyst for Enhanced CO2‐to‐CH4 Conversion by Surface Electronic Tuning DOI Open Access
Hansong Zhang, Xin‐Yue Han, Jingming Zhu

et al.

Solar RRL, Journal Year: 2025, Volume and Issue: unknown

Published: March 24, 2025

Graphitic carbon nitride (g‐C 3 N 4 ) has emerged as an attractive metal‐free photocatalyst due to its numerous advantages like tunable surface chemistry, Earth abundance, and nontoxicity. Unfortunately, photocatalytic efficiency been seriously limited by charge carrier recombination low reaction dynamics. Here, we report a BCN achieving highly selective CO 2 ‐to‐CH conversion under visible light without requiring any metal cocatalyst. The exfoliated CN nanosheets can enrich the interface with protons accelerate protonation of intermediate further produce CH . Moreover, B doping not only introduces more reactive defects but also tunes electronic structure negative conduction band for rapid electron extraction enhance conversion. Photocatalytic measurements show that production rate /CO ratio are 24 13 times higher than those bulk CN, respectively. reach 130 31 few‐layer g‐C (FL‐CN) Cu/FL‐CN, selectivity toward generation on photocatalysts ≈90%. Furthermore, sunlight driving such demonstrated. This work offers new insights design customized multifunctional 2D materials solar‐driven

Language: Английский

Citations

0

Unlocking the mystery of pulse-enhanced CO2 electroreduction on copper in carbonate media DOI

Yuexu Wu,

Heng Zhu, Wentao Wang

et al.

Journal of Energy Chemistry, Journal Year: 2025, Volume and Issue: unknown

Published: April 1, 2025

Language: Английский

Citations

0