Lattice Compression Revealed at the ≈1 nm Scale

Author:

Xu Ziwei12,Dong Hongwei1,Gu Wanmiao13,He Zhen4,Jin Fengming1,Wang Chengming5,You Qing13,Li Jin6,Deng Haiteng7,Liao Lingwen13,Chen Dong8,Yang Jun8,Wu Zhikun13ORCID

Affiliation:

1. Key Laboratory of Materials Physics Anhui Key Laboratory of Nanomaterials and Nanotechnology CAS Center for Excellence in Nanoscience Institute of Solid State Physics, HFIPS Chinese Academy of Sciences Hefei Anhui 230031 P. R. China

2. University of Science and Technology of China Hefei 230026 P. R. China

3. Institute of Physical Science and Information Technology Anhui University Hefei 230601 P. R. China

4. Department of Chemistry City University of Hong Kong and Hong Kong Branch of National Precious Metals Material Engineering Research Center (NPMM) Hong Kong 999077 P. R. China

5. Instruments' Center for Physical Science University of Science and Technology of China Hefei 230026 P. R. China

6. Tsinghua University-Peking University Joint Center for Life Sciences School of Life Sciences Tsinghua University Beijing 100084 P. R. China

7. MOE Key Laboratory of Bioinformatics School of Life Sciences Tsinghua University Beijing 100084 P. R. China

8. State Key Laboratory of Multiphase Complex Systems Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 P. R. China

Abstract

AbstractLattice tuning at the ≈1 nm scale is fascinating and challenging; for instance, lattice compression at such a minuscule scale has not been observed. The lattice compression might also bring about some unusual properties, which waits to be verified. Through ligand induction, we herein achieve the lattice compression in a ≈1 nm gold nanocluster for the first time, as detected by the single‐crystal X‐ray crystallography. In a freshly synthesized Au52(CHT)28 (CHT=S‐c−C6H11) nanocluster, the lattice distance of the (110) facet is found to be compressed from 4.51 to 3.58 Å at the near end. However, the lattice distances of the (111) and (100) facets show no change in different positions. The lattice‐compressed nanocluster exhibits superior electrocatalytic activity for the CO2 reduction reaction (CO2RR) compared to that exhibited by the same‐sized Au52(TBBT)32 (TBBT=4‐tert‐butyl‐benzenethiolate) nanocluster and larger Au nanocrystals without lattice variation, indicating that lattice tuning is an efficient method for tailoring the properties of metal nanoclusters. Further theoretical calculations explain the high CO2RR performance of the lattice‐compressed Au52(CHT)28 and provide a correlation between its structure and catalytic activity.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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