Constructing metal telluride-grafted MXene as electron “donor–acceptor” heterostructure for accelerating redox kinetics of high-efficiency Li

登录注册会员服务联系我们

Constructing metal telluride-grafted MXene as electron “donor–acceptor” heterostructure for accelerating redox kinetics of high-efficiency Li–S batteries

Published:2024 Issue:21 Volume:12 Page:12691-12701
ISSN:2050-7488
Container-title:Journal of Materials Chemistry A
language:en
Short-container-title:J. Mater. Chem. A

Author:

Li Tianli¹,Liu Yizhou²,Wang Jian³^ORCID,Hao Hua¹^ORCID,Yu Zhiyong¹^ORCID,Liu Hanxing¹^ORCID

Affiliation:

1. State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, School of Material Science and Engineering, International School of Material Science and Engineering, Wuhan University of Technology, Wuhan 430070, China

2. School of Information and Optoelectronic Science and Engineering, South China Normal University, Guangzhou 510006, P. R. China

3. Helmholtz Institute Ulm (HIU), Ulm D89081, Germany

Abstract

An electron modulation strategy of “donor–acceptor” is constructed by uniformly grafting NiTe2 onto MXene, serving as a catalyst for shuttling blockers.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/TA/D4TA01278J

Reference57 articles.

1. A review on the status and challenges of electrocatalysts in lithium-sulfur batteries

2. Designing high-energy lithium–sulfur batteries

3. Catalytic Polysulfide Conversion and Physiochemical Confinement for Lithium–Sulfur Batteries

4. Emerging Catalysts to Promote Kinetics of Lithium–Sulfur Batteries

5. Heterogeneous/Homogeneous Mediators for High-Energy-Density Lithium-Sulfur Batteries: Progress and Prospects

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP