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通过金合金化工程调控铂的轨道占据实现可逆锂氧电池

Engineering e Orbital Occupancy of Pt with Au Alloying Enables Reversible Li-O Batteries.

作者信息

Zhou Yin, Gu Qianfeng, Yin Kun, Li Yiju, Tao Lu, Tan Hao, Yang Yong, Guo Shaojun

机构信息

School of Materials Science and Engineering, Peking University, Beijing, 100871, China.

Department of Materials Science and Engineering, City University of Hong Kong, Tat Chee Avenue 83, Kowloon, Hong Kong 999077, China.

出版信息

Angew Chem Int Ed Engl. 2022 Jun 27;61(26):e202201416. doi: 10.1002/anie.202201416. Epub 2022 May 3.

Abstract

Constructing well-designed catalysts to accelerate OER catalytic activity and alleviate the charge overpotential is prevailing for achieving sophisticated Li-O batteries. Herein, we report a concept for engineering the e occupancy of Pt with M alloying (M=Au, Ru) to tune the charge overpotentials for achieving high-performance Li-O batteries. The X-ray photoelectron spectroscopy results coupled with density functional theory (DFT) calculations reveal that the highly electronegative Au can capture more e electrons from Pt, leading to less e electrons of Pt in PtAu than that in PtRu. The lower e occupancy of Pt atoms in PtAu alloys entails the upward shift of the Pt d band, which causes a strong binding strength towards the intermediates (LiO ), thereby decreasing the OER energy barrier. As a consequence, the Li-O battery with a PtAu cathode delivers a low charge overpotential of 0.36 V and superior cycle life of 220 cycles at a cutoff capacity of 1000 mAh g , which is among the best in the reported noble metal-based cathodes.

摘要

构建精心设计的催化剂以加速析氧反应(OER)催化活性并减轻电荷过电位,对于实现先进的锂氧电池至关重要。在此,我们报道了一种通过M合金化(M = Au、Ru)来调控Pt的电子占据情况以调整电荷过电位从而实现高性能锂氧电池的概念。X射线光电子能谱结果与密度泛函理论(DFT)计算表明,电负性高的Au能够从Pt捕获更多电子,使得PtAu中Pt的电子比PtRu中的少。PtAu合金中Pt原子较低的电子占据导致Pt d带向上移动,这使得对中间体(LiO)的结合强度增强,从而降低了OER能垒。结果,具有PtAu阴极的锂氧电池在截止容量为1000 mAh g时具有0.36 V的低电荷过电位和220次的优异循环寿命,这在已报道的基于贵金属的阴极中处于最佳水平。

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