J
Jiacheng Chen
Researcher at East China University of Science and Technology
Publications - 30
Citations - 928
Jiacheng Chen is an academic researcher from East China University of Science and Technology. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 9, co-authored 21 publications receiving 312 citations.
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Journal ArticleDOI
Covalently Grafting Cobalt Porphyrin onto Carbon Nanotubes for Efficient CO 2 Electroreduction
TL;DR: This work proposes a new strategy to covalently graft cobalt porphyrin onto the surface of a carbon nanotube by a substitution reaction at the metal center, providing an effective pathway for the improvement of the performance of electrocatalysts that could inspire rational design of molecular catalysts in the future.
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Cobalt phthalocyanine coordinated to pyridine-functionalized carbon nanotubes with enhanced CO2 electroreduction
TL;DR: In this article, a cobalt phthalocyanine-based catalyst supported on pyridine-functionalized carbon nanotubes (CoPc-py-CNT) was designed for electrochemical CO2 reduction.
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Synergistic Effect of Atomically Dispersed Ni-Zn Pair Sites for Enhanced CO2 Electroreduction.
Youzhi Li,Bo Wei,Minghui Zhu,Jiacheng Chen,Qike Jiang,Bin Yang,Yang Hou,Lecheng Lei,Zhongjian Li,Ruifeng Zhang,Yingying Lu +10 more
TL;DR: In situ characterization combined with density functional theory (DFT) calculations reveals that heteronuclear coordination modifies the d-states of the metal atom, resulting in a lower free energy barrier in the thermodynamic pathway and a reduced activation energy as well as fortified metal-C bonding in the kinetic pathway.
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Vacancy engineering of the nickel-based catalysts for enhanced CO2 methanation
Minghui Zhu,Pengfei Tian,Xinyu Cao,Jiacheng Chen,Tiancheng Pu,Bianfang Shi,Jing Xu,Jisue Moon,Zili Wu,Yi-Fan Han,Yi-Fan Han +10 more
TL;DR: In this article, a Y2O3-promoted NiO-CeO2 catalyst was proposed and found to exhibit an outstanding methanation activity that is up to three folds higher than NiOCe O2 and six fold higher than NO-Y 2 O3 at mild reaction temperatures.
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Structure‐Tunable Copper–Indium Catalysts for Highly Selective CO2 Electroreduction to CO or HCOOH
TL;DR: For the first time, it is reported that by varying the metal ratio, the catalyst can be tuned from a core-shell structure that selectively produces CO to a well-mixed structure that prefers HCOOH production.