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用于全解水的高效且稳定的电催化剂——同质NiSSe核壳纳米结构的晶格应变工程

Lattice-Strain Engineering of Homogeneous NiS Se Core-Shell Nanostructure as a Highly Efficient and Robust Electrocatalyst for Overall Water Splitting.

作者信息

Wang Yang, Li Xiaopeng, Zhang Mengmeng, Zhou Yuanguang, Rao Dewei, Zhong Cheng, Zhang Jinfeng, Han Xiaopeng, Hu Wenbin, Zhang Yucang, Zaghib Karim, Wang Yuesheng, Deng Yida

机构信息

School of Materials Science and Engineering, Tianjin Key Laboratory of Composite and Functional Materials, Key Laboratory of Advanced Ceramics and Machining Technology of Ministry of Education, Tianjin University, Tianjin, 300072, China.

School of Materials Science and Engineering, Jiangsu University, Zhenjiang, 212013, China.

出版信息

Adv Mater. 2020 Oct;32(40):e2000231. doi: 10.1002/adma.202000231. Epub 2020 Sep 1.

Abstract

Developing highly-efficient non-noble-metal electrocatalysts for water splitting is crucial for the development of clean and reversible hydrogen energy. Introducing lattice strain is an effective strategy to develop efficient electrocatalysts. However, lattice strain is typically co-created with heterostructure, vacancy, or substrate effects, which complicate the identification of the strain-activity correlation. Herein, a series of lattice-strained homogeneous NiS Se nanosheets@nanorods hybrids are designed and synthesized by a facile strategy. The NiS Se with ≈2.7% lattice strain exhibits outstanding activity for hydrogen and oxygen evolution reaction (HER/OER), affording low overpotentials of 70 and 257 mV at 10 mA cm , respectively, as well as excellent long-term durability even at a large current density of 100 mA cm (300 h), significantly superior to other benchmarks and the precious metal catalysts. Experimental and theoretical calculation results reveal that the generated lattice strain decreases the metal d-orbital overlap, leading to a narrower bandwidth and a closer d-band center toward the Fermi level. Thus, NiS Se possesses favorable H* adsorption kinetics for HER and lower energy barriers for OER. This work provides a new insight to regulate the lattice strain of advanced catalyst materials and further improve the performance of energy conversion technologies.

摘要

开发用于水分解的高效非贵金属电催化剂对于清洁和可逆氢能的发展至关重要。引入晶格应变是开发高效电催化剂的有效策略。然而,晶格应变通常与异质结构、空位或基底效应共同产生,这使得应变-活性相关性的识别变得复杂。在此,通过一种简便的策略设计并合成了一系列具有晶格应变的均匀NiS Se纳米片@纳米棒杂化物。具有约2.7%晶格应变的NiS Se对析氢反应和析氧反应(HER/OER)表现出出色的活性,在10 mA cm 时分别提供70和257 mV的低过电位,以及即使在100 mA cm 的大电流密度下(300 h)也具有出色的长期耐久性,明显优于其他基准和贵金属催化剂。实验和理论计算结果表明,产生的晶格应变降低了金属d轨道重叠,导致带宽变窄且d带中心更接近费米能级。因此,NiS Se对HER具有良好的H*吸附动力学,对OER具有较低的能垒。这项工作为调控先进催化剂材料的晶格应变和进一步提高能量转换技术的性能提供了新的见解。

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