Atomically dispersed Ni activates adjacent Ce sites for enhanced electrocatalytic oxygen evolution activity

Author:

Pei Zhihao1ORCID,Zhang Huabin2ORCID,Wu Zhi-Peng2ORCID,Lu Xue Feng3ORCID,Luan Deyan1ORCID,Lou Xiong Wen (David)4ORCID

Affiliation:

1. School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, 62 Nanyang Drive, Singapore 637459, Singapore.

2. KAUST Catalysis Center (KCC), King Abdullah University of Science and Technology (KAUST), Thuwal 23955-6900, Saudi Arabia.

3. State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou 350002, China.

4. Department of Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon 999077, Hong Kong, China.

Abstract

Manipulating the intrinsic activity of heterogeneous catalysts at the atomic level is an effective strategy to improve the electrocatalytic performances but remains challenging. Here, atomically dispersed Ni anchored on CeO 2 particles entrenched on peanut-shaped hollow nitrogen-doped carbon structures ( a -Ni/CeO 2 @NC) is rationally designed and synthesized. The as-prepared a -Ni/CeO 2 @NC catalyst exhibits substantially boosted intrinsic activity and greatly reduced overpotential for the electrocatalytic oxygen evolution reaction. Experimental and theoretical results demonstrate that the decoration of isolated Ni species over the CeO 2 induces electronic coupling and redistribution, thus resulting in the activation of the adjacent Ce sites around Ni atoms and greatly accelerated oxygen evolution kinetics. This work provides a promising strategy to explore the electronic regulation and intrinsic activity improvement at the atomic level, thereby improving the electrocatalytic activity.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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