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Highly Efficient Nb 2 C MXene Cathode Catalyst with Uniform O‐Terminated Surface for Lithium–Oxygen Batteries
Author(s) -
Li Gaoyang,
Li Na,
Peng Shuting,
He Biao,
Wang Jun,
Du Yong,
Zhang Weibin,
Han Kai,
Dang Feng
Publication year - 2021
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202002721
Subject(s) - mxenes , materials science , overpotential , catalysis , cathode , lithium (medication) , chemical engineering , density functional theory , oxygen evolution , nanotechnology , electrode , chemistry , electrochemistry , computational chemistry , medicine , endocrinology , engineering , biochemistry
Highly‐efficient cathode catalysts are the key to improve high rate cycle stability, avoid side reactions, and lower the overpotential of lithium–oxygen batteries (LOBs). MXenes are predicted to be one of the most impressive materials for energy applications. In this work, the catalytic capability of Nb 2 C MXene is demonstrated with a uniform O‐terminated surface as a cathode material for LOBs. The easily fabricated uniform O‐terminated surface, high catalytic activity of Nb 2 CO 2 sites, and unique reaction kinetics contribute to the excellent electrocatalytic performance of Nb 2 C MXene. The uniform O‐terminated surface on Nb 2 C MXene is obtained after heat treatment. Density functional theory calculations reveal the superior catalytic activity of Nb 2 CO 2 compared to other anchor groups and bare surfaces. The calculations also reveal the multinucleation and growth/decomposition mechanism for discharge products on the Nb 2 CO 2 surface. This mechanism is believed to account for the results characterized by ex situ and in situ measurements. The spatial‐direction accumulated porous discharge products at high current density contribute to the excellent high‐rate cycle stability. For example, the cathodes exhibit cycle stability for 130 cycles at an ultrahigh current density of 3 A g −1 . The present work provides insights into the modulation of catalytic capabilities, and the rational design of high‐performance MXenes based electrocatalysts.

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