Asymmetric Cu<sub>1</sub>-N<sub>3</sub>-P-C active centers for efficient acetylene hydrochlorination

We investigated the pivotal role of active center symmetry on the stability of reactant adsorption and the transition state dynamics within the context of acetylene hydrochlorination. Our innovative approach involved the integration of phosphorus into a nitrogen-doped carbon framework and introduced the single Cu center, culminating in the development of novel copper-nitrogen-phosphorus-carbon (Cu-NPC) catalysts. These catalysts are distinguished by their asymmetrical Cu<sub>1</sub>-N<sub>3</sub>-P-C chemical environment. Our kinetic studies shed light on the underlying mechanisms contributing to the superior performance of the Cu-NPC catalysts. These catalysts not only enhance the reaction rate by moderating the adsorption strength of reactants, thereby optimizing the reaction kinetics, but also demonstrate an outstanding ability to mitigate the risk of carbon deposition, a common challenge that compromises catalyst longevity and efficiency. This is evidenced by a notably low deactivation rate of 0.027 h<sup>−1</sup> at a high C<sub>2</sub>H<sub>2</sub> weight hourly space velocity (WHSV) of 1.4 <inline-formula id="M1"> <math id="mathml_M1" display="inline" overflow="scroll"><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>g</mtext></mrow><mrow class="MJX-TeXAtom-ORD"><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>C</mtext></mrow><mn>2</mn></msub></mrow><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>H</mtext></mrow><mn>2</mn></msub></mrow></mrow></msub></mrow><mo>⋅</mo><msup><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>g</mtext></mrow><mrow class="MJX-TeXAtom-ORD"><mrow class="MJX-TeXAtom-ORD"><mtext>cat</mtext></mrow></mrow></msub></mrow><mrow class="MJX-TeXAtom-ORD"><mo>−</mo><mn>1</mn></mrow></msup><mo>⋅</mo><mrow class="MJX-TeXAtom-ORD"><msup><mrow class="MJX-TeXAtom-ORD"><mtext>h</mtext></mrow><mrow class="MJX-TeXAtom-ORD"><mo>−</mo><mn>1</mn></mrow></msup></mrow></math></inline-formula>. This research not only advances our understanding of the critical influence of active center symmetry on catalyst performance but also paves the way for the rational design of advanced catalysts tailored for specific industrial applications.

Authors

Institutions

Publication Details

Journal
Carbon Future
Published
2025-02-24
DOI
https://doi.org/10.26599/cf.2025.9200040
Primary Topic
Catalysis and Oxidation Reactions
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Asymmetric Cu1-N3-P-C active centers for efficient acetylene hydrochlorination

Mengxin Wang, Yuxiang Bao, Zhe Ma, Xiuhui Zheng et al.
Carbon Future
Catalysis and Oxidation Reactions
article

Asymmetric Cu1-N3-P-C active centers for efficient acetylene hydrochlorination

Mengxin Wang, Yuxiang Bao, Zhe Ma, Xiuhui Zheng, De Chen, Juncong Yuan, Xiang Feng, Baorui Li, Xiaobo Chen, Yongxiao Tuo, Xing Lv, Chang Liu, Lina Li, Jianlin Cao, Yibin Liu, Yanying Gao, Hao Yan, Y.Q. Guo, Chaohe Yang
article en

Abstract

We investigated the pivotal role of active center symmetry on the stability of reactant adsorption and the transition state dynamics within the context of acetylene hydrochlorination. Our innovative approach involved the integration of phosphorus into a nitrogen-doped carbon framework and introduced the single Cu center, culminating in the development of novel copper-nitrogen-phosphorus-carbon (Cu-NPC) catalysts. These catalysts are distinguished by their asymmetrical Cu<sub>1</sub>-N<sub>3</sub>-P-C chemical environment. Our kinetic studies shed light on the underlying mechanisms contributing to the superior performance of the Cu-NPC catalysts. These catalysts not only enhance the reaction rate by moderating the adsorption strength of reactants, thereby optimizing the reaction kinetics, but also demonstrate an outstanding ability to mitigate the risk of carbon deposition, a common challenge that compromises catalyst longevity and efficiency. This is evidenced by a notably low deactivation rate of 0.027 h<sup>−1</sup> at a high C<sub>2</sub>H<sub>2</sub> weight hourly space velocity (WHSV) of 1.4 <inline-formula id="M1"> <math id="mathml_M1" display="inline" overflow="scroll"><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>g</mtext></mrow><mrow class="MJX-TeXAtom-ORD"><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>C</mtext></mrow><mn>2</mn></msub></mrow><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>H</mtext></mrow><mn>2</mn></msub></mrow></mrow></msub></mrow><mo>⋅</mo><msup><mrow class="MJX-TeXAtom-ORD"><msub><mrow class="MJX-TeXAtom-ORD"><mtext>g</mtext></mrow><mrow class="MJX-TeXAtom-ORD"><mrow class="MJX-TeXAtom-ORD"><mtext>cat</mtext></mrow></mrow></msub></mrow><mrow class="MJX-TeXAtom-ORD"><mo>−</mo><mn>1</mn></mrow></msup><mo>⋅</mo><mrow class="MJX-TeXAtom-ORD"><msup><mrow class="MJX-TeXAtom-ORD"><mtext>h</mtext></mrow><mrow class="MJX-TeXAtom-ORD"><mo>−</mo><mn>1</mn></mrow></msup></mrow></math></inline-formula>. This research not only advances our understanding of the critical influence of active center symmetry on catalyst performance but also paves the way for the rational design of advanced catalysts tailored for specific industrial applications.

Carbon FutureVol. 2(1)
China University of Petroleum, Beijing (CN), Norwegian University of Science and Technology (NO), Shanghai Advanced Research Institute (CN), Shanghai Institute of Applied Physics (CN), Dezhou University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Shandong Province
Openalex Percentile: Top 99%
Catalysis and Oxidation Reactions
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.