期刊
ADVANCED MATERIALS
卷 34, 期 27, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202202084
关键词
atomic-scale materials; coordination number; defect engineering; oxygen reduction reaction; Pd nanosheet
类别
资金
- National Key R&D Program of China [2021YFA1501001]
- National Science Fund for Distinguished Young Scholars [52025133]
- Tencent Foundation through the XPLORER PRIZE
Moderate adsorption of oxygenated intermediates plays a crucial role in the rational design of high-efficiency oxygen reduction reaction (ORR) electrocatalysts. Defect engineering, which can adjust the coordination environment of catalytic active sites, is a reliable strategy for tuning the geometric structure of nanomaterials. However, it remains challenging to uniformly disperse high-coordinated defects into ultrathin 2D nanosheets due to the limitations of controllable nanocrystal fabrication. This study introduces atomic-scale cavities (ASCs) as a new type of high-coordinated active site and successfully incorporates them into suprathin Pd (111)-exposed metallene for enhanced ORR performance.
Moderate adsorption of oxygenated intermediates takes a significant role in rational design of high-efficiency oxygen reduction reaction (ORR) electrocatalysts. Long-serving as a reliable strategy to tune geometric structure of nanomaterials, defect engineering enjoys the great ability of adjusting the coordination environment of catalytic active sites, which enables dominant regulation of adsorption energy and kinetics of ORR catalysis. However, limited to controllable nanocrystals fabrication, inducing uniformly dispersed high-coordinated defects into ultrathin 2D nanosheets remains challenging. Herein, atomic-scale cavities (ASCs) are proposed as a new kind of high-coordinated active site and successfully introduced into suprathin Pd (111)-exposed metallene. Due to its atomic concave architecture, leading to elevated CN and moderately downshifted d-band center, the as-made Pd metallene with ASCs (c-Pd M) exhibits excellent ORR performance with mass activity of 2.76 A mg(Pd)(-1) at 0.9 V versus reversible hydrogen electrode (RHE) and half-wave potential as high as 0.947 V, which is 18.9 (2.7) times higher and 104 (46) mV larger than that of commercial Pt/C (Pd metallene without ASCs). Besides, the durability of c-Pd M exceeds its commercial counterpart with approximate to 30% loss after 5000 cycles. This work highlights a new-style mentality of designing fancy active sites toward efficient ORR electrocatalysis.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据