Xia Zhonghong, Guo Shaojun
Department of Materials Science & Engineering, College of Engineering, Peking University, Beijing 100871, China.
Chem Soc Rev. 2019 Jun 17;48(12):3265-3278. doi: 10.1039/c8cs00846a.
The strain effect, along with the ligand effect and synergistic effect, contributes primarily to the optimization of electrocatalytic activity and stability. The strain effect leads to a shift in the d-band center and alters binding energies toward adsorbates. Under electrocatalytic circumstances, the strain effect and ligand effect by and large function in combination; however, the decay and vanishing of the ligand effect precede the strain effect as the thickness of the shell in the core/shell structure or metallic overlayers on substrates increases. The strain effect on electrocatalytic activity can be well engineered by tuning the thickness of shells or atomic composition. Microstrain, or localized lattice strain, is another type of strain associated with structural defects such as grain boundaries and multi-twinning. In this review, we discuss the origin of the strain effect and how it affects electrocatalytic activity based on the d-band model. We present the structural characterization and quantitative determination of strain. Metal-based nanocrystals are basically grouped into two types of structures to which the strain engineering applies, i.e. lattice strain-associated structures (which include the general core/shell structure and solid solution alloy) and multiple defects-induced structures. Then analysis is performed on the correlation of strain and ligand effects and on the tuning strategies of the strain effect for electrocatalysis. After that, we use representative examples to demonstrate how strain engineering assists in typical electrocatalytic reactions on anodes and cathodes. Finally, we summarize and propose potential research areas in terms of enhancing electrocatalytic activities by strain engineering in the future.
应变效应与配体效应和协同效应一起,主要有助于优化电催化活性和稳定性。应变效应导致d带中心发生位移,并改变对吸附质的结合能。在电催化条件下,应变效应和配体效应大体上共同起作用;然而,随着核壳结构中壳层厚度或基底上金属覆盖层厚度的增加,配体效应的衰减和消失先于应变效应。通过调节壳层厚度或原子组成,可以很好地调控应变效应对电催化活性的影响。微应变,即局部晶格应变,是另一种与诸如晶界和多重孪晶等结构缺陷相关的应变类型。在本综述中,我们基于d带模型讨论应变效应的起源及其如何影响电催化活性。我们介绍了应变的结构表征和定量测定。基于金属的纳米晶体基本上分为应变工程适用的两种结构类型,即晶格应变相关结构(包括一般的核壳结构和固溶体合金)和多重缺陷诱导结构。然后分析了应变与配体效应的相关性以及应变效应在电催化中的调控策略。之后,我们用代表性的例子展示应变工程如何辅助阳极和阴极上的典型电催化反应。最后,我们总结并提出了未来通过应变工程提高电催化活性方面潜在的研究领域。