TY - JOUR
T1 - Cold-plasma technique enabled supported Pt single atoms with tunable coordination for hydrogen evolution reaction
AU - Li, Jing
AU - Zhou, Yanan
AU - Tang, Weijing
AU - Zheng, Jian
AU - Gao, Xiaoping
AU - Wang, Ning
AU - Chen, Xiao
AU - Wei, Min
AU - Xiao, Xin
AU - Chu, Wei
N1 - KAUST Repository Item: Exported on 2021-01-14
Acknowledgements: J. Li, Y. Zhou, and W. Tang contributed equally to this work. We acknowledge the financial support from the National Natural Science Foundation of China (21872098). The State Key Laboratory of Polymer Materials Engineering at Sichuan University is acknowledged for providing Dmol3 modules.
PY - 2020/12
Y1 - 2020/12
N2 - Coordination tunability of the single-atom catalysts (SACs) is an essential but challenging issue for the catalyst sifting and structure-activity relationship analysis. Herein, Pt single atoms with tunable coordination are readily achieved via a facile cold-plasma technique by changing the gas type (N2, Ar, or Air) and treatment duration. Combining with density functional theory calculation, the Pt-N coordination concentration is predicted to be highly correlated with adsorption free energy of H* atoms (ΔGH*) for the hydrogen evolution reaction (HER), which is further validated experimentally. Remarkably, the sample with N, O co-dopant introduced by air plasma exhibits a high TOF of ∼13 H2 s−1 at 40 mV, and outstanding mass activity of 7.41 A mg−1Pt for HER, which is 26.5 times of commercial Pt/C catalyst. The enhanced performance might originate from the optimized electronic structure of active carbon site with moderate electron transfer and p-band center, which enables a suitable binding strength with H* and thus a near-zero ΔGH*.
AB - Coordination tunability of the single-atom catalysts (SACs) is an essential but challenging issue for the catalyst sifting and structure-activity relationship analysis. Herein, Pt single atoms with tunable coordination are readily achieved via a facile cold-plasma technique by changing the gas type (N2, Ar, or Air) and treatment duration. Combining with density functional theory calculation, the Pt-N coordination concentration is predicted to be highly correlated with adsorption free energy of H* atoms (ΔGH*) for the hydrogen evolution reaction (HER), which is further validated experimentally. Remarkably, the sample with N, O co-dopant introduced by air plasma exhibits a high TOF of ∼13 H2 s−1 at 40 mV, and outstanding mass activity of 7.41 A mg−1Pt for HER, which is 26.5 times of commercial Pt/C catalyst. The enhanced performance might originate from the optimized electronic structure of active carbon site with moderate electron transfer and p-band center, which enables a suitable binding strength with H* and thus a near-zero ΔGH*.
UR - http://hdl.handle.net/10754/666885
UR - https://linkinghub.elsevier.com/retrieve/pii/S0926337320312789
UR - http://www.scopus.com/inward/record.url?scp=85098657533&partnerID=8YFLogxK
U2 - 10.1016/j.apcatb.2020.119861
DO - 10.1016/j.apcatb.2020.119861
M3 - Article
SN - 0926-3373
VL - 285
SP - 119861
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
ER -