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Atomically-precise dopant-controlled single cluster catalysis for electrochemical nitrogen reduction.

Authors :
Yao, Chuanhao
Guo, Na
Xi, Shibo
Xu, Cong-Qiao
Liu, Wei
Zhao, Xiaoxu
Li, Jing
Fang, Hanyan
Su, Jie
Chen, Zhongxin
Yan, Huan
Qiu, Zhizhan
Lyu, Pin
Chen, Cheng
Xu, Haomin
Peng, Xinnan
Li, Xinzhe
Liu, Bin
Su, Chenliang
Pennycook, Stephen J.
Source :
Nature Communications; 9/1/2020, Vol. 11 Issue 1, pN.PAG-N.PAG, 1p
Publication Year :
2020

Abstract

The ability to precisely engineer the doping of sub-nanometer bimetallic clusters offers exciting opportunities for tailoring their catalytic performance with atomic accuracy. However, the fabrication of singly dispersed bimetallic cluster catalysts with atomic-level control of dopants has been a long-standing challenge. Herein, we report a strategy for the controllable synthesis of a precisely doped single cluster catalyst consisting of partially ligand-enveloped Au<subscript>4</subscript>Pt<subscript>2</subscript> clusters supported on defective graphene. This creates a bimetal single cluster catalyst (Au<subscript>4</subscript>Pt<subscript>2</subscript>/G) with exceptional activity for electrochemical nitrogen (N<subscript>2</subscript>) reduction. Our mechanistic study reveals that each N<subscript>2</subscript> molecule is activated in the confined region between cluster and graphene. The heteroatom dopant plays an indispensable role in the activation of N<subscript>2</subscript> via an enhanced back donation of electrons to the N<subscript>2</subscript> LUMO. Moreover, besides the heteroatom Pt, the catalytic performance of single cluster catalyst can be further tuned by using Pd in place of Pt as the dopant. The fabrication of singly dispersed metal cluster catalysts with atomic-level control of dopants is a long-standing challenge. Here, the authors report a strategy for the synthesis of a precisely doped single cluster catalyst which shows exceptional activity for electrochemical dinitrogen reduction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
11
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
145433476
Full Text :
https://doi.org/10.1038/s41467-020-18080-w