Kinetic‐Modulated Crystal Phase of Ru for Hydrogen Oxidation

Author:

Zhang Juntao1,Cao Maofeng1,Li Xiaotong2,Xu Yong3ORCID,Zhao Wei4,Chen Ligang4,Chang Yu‐Chung5,Pao Chih‐Wen5,Hu Zhiwei6,Huang Xiaoqing1

Affiliation:

1. State Key Laboratory of Physical Chemistry of Solid Surfaces College of Chemistry and Chemical Engineering Xiamen University Xiamen 361005 P. R. China

2. State Key Joint Laboratory of Environment Simulation and Pollution Control Research Center for Eco‐Environmental Sciences Chinese Academy of Sciences Beijing 100085 P. R. China

3. Guangzhou Key Laboratory of Low‐Dimensional Materials and Energy Storage Devices Collaborative Innovation Center of Advanced Energy Materials School of Materials and Energy Guangdong University of Technology Guangzhou 510006 P. R. China

4. State Power Investment Corporation Hydrogen Energy Company, Limited Beijing 102209 P. R. China

5. National Synchrotron Radiation Research Center 101 Hsin‐Ann Road Hsinchu 30076 Taiwan

6. Max Planck Institute for Chemical Physics of Solids Nothnitzer Strasse 40 01187 Dresden Germany

Abstract

AbstractCrystal‐phase‐engineering provides a powerful strategy for regulating the catalytic performance yet remains great challenge. Herein, the kinetic‐modulated crystal‐phase‐control of Ru nanosheet assemblies (Ru NAs) is demonstrated by simply altering the concentration of citric acid (CA). Detailed experimental results reveal that high concentration of CA retards the growth kinetics and thus leads to the formation of metastable face‐centered cubic (fcc) Ru NAs, while low concentration of CA results in the fast growth kinetics and the preferential formation of Ru NAs with stable hexagonal close packed (hcp) phase. Moreover, Ru NAs with different phases are used as catalyst for hydrogen oxidation reaction (HOR) to evaluate the effects of crystal phase on catalytic performance. Impressively, Ru NAs with fcc phase display a mass activity of 2.75 A mgRu−1 at 50 mV, which is much higher than those of Ru NAs with fcc/hcp (1.02 A mgRu−1) and hcp (0.74 A mgRu−1) phases. Theoretical calculations show that fcc Ru NAs display weaker adsorption toward *H and lower energy barrier toward the rate‐determining step (RDS) during HOR. This work provides a facile strategy for regulating the crystal phase of Ru nanocrystals, which may attract rapid interests of researchers in materials, chemistry, and catalysis.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Natural Science Foundation of Guangdong Province for Distinguished Young Scholars

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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