Synthesis of ethane from CO 2 by a methyl transferase–inspired molecular catalyst DOI Creative Commons
Suman Patra,

Souvik Dinda,

Soumili Ghosh

et al.

Proceedings of the National Academy of Sciences, Journal Year: 2025, Volume and Issue: 122(2)

Published: Jan. 7, 2025

Molecular catalysts with a single metal center are reported to reduce CO 2 wide range of valuable single-carbon products like CO, HCOOH, CH 3 OH, etc. However, these cannot two carbon ethane or ethylene and the ability form C–C from remains mostly limited heterogeneous material-based catalysts. We report set simple iron porphyrins pendant thiol group can catalyze reduction (C H 6 ) O as proton source Faradaic yield >40% rest being CO. The mechanism involves -derived methyl transfer akin proposal forwarded for transferases follow-up bond formation thioether thus formed Fe(II)–CH species generated by second molecule . availability “parking space” in molecular framework first reduced C 1 product allows resulting unique case where component natural gas be direct electrochemical

Language: Английский

Review on strategies for improving the added value and expanding the scope of CO2 electroreduction products DOI
Minghang Jiang, Huaizhu Wang, Mengfei Zhu

et al.

Chemical Society Reviews, Journal Year: 2024, Volume and Issue: 53(10), P. 5149 - 5189

Published: Jan. 1, 2024

This review summarizes promising strategies including the design of catalysts and construction coupled electrocatalytic reaction systems, aimed at achieving selective production various products from CO 2 electroreduction.

Language: Английский

Citations

70

Atomic Engineering of Single‐Atom Nanozymes for Biomedical Applications DOI

Ji Shen,

Jian Chen, Yuping Qian

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: 36(21)

Published: Feb. 7, 2024

Single-atom nanozymes (SAzymes) showcase not only uniformly dispersed active sites but also meticulously engineered coordination structures. These intricate architectures bestow upon them an exceptional catalytic prowess, thereby captivating numerous minds and heralding a new era of possibilities in the biomedical landscape. Tuning microstructure SAzymes on atomic scale is key factor designing targeted with desirable functions. This review first discusses summarizes three strategies for their impact reactivity biocatalysis. The effects choices carrier, different synthesis methods, modulation first/second shell, type number metal centers enzyme-like activity are unraveled. Next, attempt made to summarize biological applications tumor therapy, biosensing, antimicrobial, anti-inflammatory, other from mechanisms. Finally, how designed regulated further realization diverse reviewed prospected. It envisaged that comprehensive presented within this exegesis will furnish novel perspectives profound revelations regarding SAzymes.

Language: Английский

Citations

50

General Design Concept of High‐Performance Single‐Atom‐Site Catalysts for H2O2 Electrosynthesis DOI

Mingyang Deng,

Dingsheng Wang, Yadong Li

et al.

Advanced Materials, Journal Year: 2024, Volume and Issue: 36(24)

Published: March 5, 2024

Hydrogen peroxide (H

Language: Английский

Citations

27

Steering the Reaction Pathway of CO2 Electroreduction by Tuning the Coordination Number of Copper Catalysts DOI

Jiapeng Jiao,

Xinchen Kang, Jiahao Yang

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(23), P. 15917 - 15925

Published: May 28, 2024

Cu-based catalysts are optimal for the electroreduction of CO2 to generate hydrocarbon products. However, controlling product distribution remains a challenging topic. The theoretical investigations have revealed that coordination number (CN) Cu considerably influences adsorption energy *CO intermediates, thereby affecting reaction pathway. with different CNs were fabricated by reducing CuO precursors via cyclic voltammetry (Cyc-Cu), potentiostatic electrolysis (Pot-Cu), and pulsed (Pul-Cu), respectively. High-CN predominantly C2+ products, while low-CN favors CH4 production. For instance, over high-CN Pot-Cu, is main product, Faradaic efficiency (FE) reaching 82.5% partial current density (j) 514.3 mA cm–2. Conversely, Pul(3)-Cu production CH4, achieving highest FECH4 value 56.7% jCH4 234.4 In situ X-ray absorption spectroscopy Raman studies further confirm adsorptions CN, directing pathway CO2RR.

Language: Английский

Citations

27

Highly Selective Electrocatalytic CO2 Conversion to Tailored Products through Precise Regulation of Hydrogenation and C–C Coupling DOI

Chenfeng Xia,

Tao Wang, Chaohui He

et al.

Journal of the American Chemical Society, Journal Year: 2024, Volume and Issue: 146(29), P. 20530 - 20538

Published: July 11, 2024

The electrochemical reduction reaction of carbon dioxide (CO

Language: Английский

Citations

27

Atomically dispersed multi-site catalysts: bifunctional oxygen electrocatalysts boost flexible zinc–air battery performance DOI
Shengchen Wang, Mengyang Zhang,

Xueqin Mu

et al.

Energy & Environmental Science, Journal Year: 2024, Volume and Issue: 17(14), P. 4847 - 4870

Published: Jan. 1, 2024

Based on the advancements in atomically dispersed multi-site catalysts for FZABs, this review discusses design methodologies to regulate performance of bifunctional oxygen electrocatalysts from electronic and geometric structures.

Language: Английский

Citations

21

Steering the Site Distance of Atomic Cu‐Cu Pairs by First‐Shell Halogen Coordination Boosts CO2‐to‐C2 Selectivity DOI Open Access

Fengya Ma,

Pengfang Zhang,

Xiaobo Zheng

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(46)

Published: Aug. 6, 2024

Electrocatalytic reduction of CO

Language: Английский

Citations

20

Modification of the CuO electronic structure for enhanced selective electrochemical CO2 reduction to ethylene DOI
Xin Wu,

Zhuang Tong,

Yunliang Liu

et al.

Nano Research, Journal Year: 2024, Volume and Issue: 17(8), P. 7194 - 7202

Published: June 1, 2024

Language: Английский

Citations

19

Copper Atom Pairs Stabilize *OCCO Dipole Toward Highly Selective CO2 Electroreduction to C2H4 DOI Open Access
Shenghua Chen,

Xiaobo Zheng,

Peng Zhu

et al.

Angewandte Chemie International Edition, Journal Year: 2024, Volume and Issue: 63(50)

Published: Aug. 13, 2024

Abstract Deeply electrolytic reduction of carbon dioxide (CO 2 ) to high‐value ethylene (C H 4 is very attractive. However, the sluggish kinetics C−C coupling seriously results in low selectivity CO electroreduction C . Herein, we report a copper‐based polyhedron (Cu2) that features uniformly distributed and atomically precise bi‐Cu units, which can stabilize *OCCO dipole facilitate for high selective production. The faradaic efficiency (FE) reaches 51 % with current density 469.4 mA cm −2 , much superior Cu single site catalyst (Cu SAC) (~0 %). Moreover, Cu2 has higher turnover frequency (TOF, ~520 h −1 compared nanoparticles (~9.42 SAC (~0.87 ). In situ characterizations theoretical calculations revealed unique structural configuration could optimize moments adsorbate promote generation

Language: Английский

Citations

19

Targeted C-O bond cleavage of *CH2CHO at copper active sites for efficient electrosynthesis of ethylene from CO2 reduction DOI
Huiying Zhang, Xiaojun Wang,

Yanfei Sun

et al.

Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 351, P. 123992 - 123992

Published: April 24, 2024

Language: Английский

Citations

17