Enhanced CO2 electroreduction with conjugation effect tuned atomically dispersed nickel-based catalysts

被引:3
|
作者
Song, Qian [1 ]
Guo, Bowen [2 ,3 ]
Liu, Hang [1 ]
Wang, Hongguang [4 ]
Schmidt, Maximilian [1 ]
van Aken, Peter A. [4 ]
Luo, Dan [2 ]
Klemm, Elias [1 ]
机构
[1] Univ Stuttgart, Inst Tech Chem, D-70569 Stuttgart, Germany
[2] Chinese Acad Sci, CAS Ctr Excellence Nanosci, Beijing Inst Nanoenergy & Nanosyst, Beijing Key Lab Micronano Energy & Sensor, Beijing 101400, Peoples R China
[3] China Univ Petr, Coll New Energy & Mat, Beijing 102249, Peoples R China
[4] Max Planck Inst Solid State Res, D-70569 Stuttgart, Germany
来源
CELL REPORTS PHYSICAL SCIENCE | 2023年 / 4卷 / 12期
关键词
OXYGEN REDUCTION; SITES;
D O I
10.1016/j.xcrp.2023.101737
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tuning the coordination number and coordinating atoms is a general strategy to control the activity of single-atom catalysts; however, this method has encountered bottlenecks in investigating the atomically dispersed Ni-N-C catalysts for efficient electrochem-ical CO2 reduction reaction (eCO2RR). Herein, we propose a strategy by modulating a ligand-conjugated structure to improve the activity of Ni-based single-atom catalysts without changing the coordinated atoms and coordination numbers. In the pyrrole-type Ni-N-C cata-lyst (Ni-NPyrrolic-C), the electron-donating conjugation effect of the pyrrole ligand reduces the electron cloud density on the N atom, re-sulting in stronger electron depletion around the active center Ni atom and thereby improving activity of CO2 electroreduction to CO. The Ni-NPyrrolic-C possesses a notable CO partial current density of 415 mA cm -2 with 92% CO Faradaic efficiency (FE) at a moderate potential of-0.85 V in gas diffusion electrodes (GDEs), which outperforms the pyridinic-type Ni-N-C catalyst (Ni-NPyridinic-C) with electron-withdrawing conjugation effect ligands.
引用
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页数:15
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