Details
Original language | English |
---|---|
Article number | 2302626 |
Journal | Advanced functional materials |
Volume | 34 |
Issue number | 5 |
Publication status | Published - 29 Jan 2024 |
Abstract
Room-temperature sodium–sulfur (RT Na–S) batteries have emerged as a promising candidate for next-generation scalable energy storage systems, due to their high theoretical energy density, low cost, and natural abundance. However, the practical applications of these batteries are hindered by the notorious shuttle effect of soluble sodium polysulfides (NaPSs) and sluggish reaction kinetics, which result in fast performance loss. To address this issue, recent studies have reported impressive achievements of transition metal nanoparticles/single atoms/cluster/compounds (TM)-based host materials with strong adsorption and catalyzation to NaPSs. These materials can significantly improve the electrochemical performance of RT Na–S batteries. In this review, the recent progress on TM-based host materials for RT Na–S batteries, including iron (Fe)-, cobalt (Co)-, nickel (Ni)-, molybdenum (Mo)-, titanium (Ti)-, vanadium (V)-, manganese (Mn)-, and other TM-based materials are summarized. The design, fabrication, and properties of these host materials are comprehensively summarized and systematically analyzed the underlying chemical inhibition and electrocatalysis mechanism between NaPSs and TM-based catalytic materials. At last, the challenges and prospects for designing efficient TM-based catalytic materials for high-performance RT Na–S batteries are discussed.
Keywords
- catalytic materials, room-temperature sodium–sulfur batteries, shuttle effects, sluggish kinetics, transition metal nanoparticles/compounds
ASJC Scopus subject areas
- Materials Science(all)
- Electronic, Optical and Magnetic Materials
- Chemistry(all)
- Materials Science(all)
- Biomaterials
- Materials Science(all)
- Physics and Astronomy(all)
- Condensed Matter Physics
- Chemistry(all)
- Electrochemistry
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In: Advanced functional materials, Vol. 34, No. 5, 2302626, 29.01.2024.
Research output: Contribution to journal › Review article › Research › peer review
}
TY - JOUR
T1 - Recent Advances in Transition-Metal-Based Catalytic Material for Room-Temperature Sodium–Sulfur Batteries
AU - Bettels, Frederik
AU - Lin, Zhihua
AU - Li, Zhenhu
AU - Shao, Yaxin
AU - Ding, Fei
AU - Liu, Shuangyi
AU - Zhang, Lin
AU - Liu, Yuping
N1 - Funding Information: Y.L., F.B., and Z.H.L. contributed equally to this work. L.Z. conceived the project. This work was financially supported by the Ministry for Science and Culture of Lower Saxony (MWK), via the Research Training Group “CircularLIB” and the program “Nanomaterials and Quantum Technology for Digital Transformation” (hsn‐digital). Y. L. thanks the research support from the CAS “Hundred Talents Program B,” and Chongqing Institute of Green and Intelligent Technology (No. E2906216). Z.H.L. acknowledges the support from the Chinese Scholarship Council (CSC).
PY - 2024/1/29
Y1 - 2024/1/29
N2 - Room-temperature sodium–sulfur (RT Na–S) batteries have emerged as a promising candidate for next-generation scalable energy storage systems, due to their high theoretical energy density, low cost, and natural abundance. However, the practical applications of these batteries are hindered by the notorious shuttle effect of soluble sodium polysulfides (NaPSs) and sluggish reaction kinetics, which result in fast performance loss. To address this issue, recent studies have reported impressive achievements of transition metal nanoparticles/single atoms/cluster/compounds (TM)-based host materials with strong adsorption and catalyzation to NaPSs. These materials can significantly improve the electrochemical performance of RT Na–S batteries. In this review, the recent progress on TM-based host materials for RT Na–S batteries, including iron (Fe)-, cobalt (Co)-, nickel (Ni)-, molybdenum (Mo)-, titanium (Ti)-, vanadium (V)-, manganese (Mn)-, and other TM-based materials are summarized. The design, fabrication, and properties of these host materials are comprehensively summarized and systematically analyzed the underlying chemical inhibition and electrocatalysis mechanism between NaPSs and TM-based catalytic materials. At last, the challenges and prospects for designing efficient TM-based catalytic materials for high-performance RT Na–S batteries are discussed.
AB - Room-temperature sodium–sulfur (RT Na–S) batteries have emerged as a promising candidate for next-generation scalable energy storage systems, due to their high theoretical energy density, low cost, and natural abundance. However, the practical applications of these batteries are hindered by the notorious shuttle effect of soluble sodium polysulfides (NaPSs) and sluggish reaction kinetics, which result in fast performance loss. To address this issue, recent studies have reported impressive achievements of transition metal nanoparticles/single atoms/cluster/compounds (TM)-based host materials with strong adsorption and catalyzation to NaPSs. These materials can significantly improve the electrochemical performance of RT Na–S batteries. In this review, the recent progress on TM-based host materials for RT Na–S batteries, including iron (Fe)-, cobalt (Co)-, nickel (Ni)-, molybdenum (Mo)-, titanium (Ti)-, vanadium (V)-, manganese (Mn)-, and other TM-based materials are summarized. The design, fabrication, and properties of these host materials are comprehensively summarized and systematically analyzed the underlying chemical inhibition and electrocatalysis mechanism between NaPSs and TM-based catalytic materials. At last, the challenges and prospects for designing efficient TM-based catalytic materials for high-performance RT Na–S batteries are discussed.
KW - catalytic materials
KW - room-temperature sodium–sulfur batteries
KW - shuttle effects
KW - sluggish kinetics
KW - transition metal nanoparticles/compounds
UR - http://www.scopus.com/inward/record.url?scp=85164511784&partnerID=8YFLogxK
U2 - 10.1002/adfm.202302626
DO - 10.1002/adfm.202302626
M3 - Review article
AN - SCOPUS:85164511784
VL - 34
JO - Advanced functional materials
JF - Advanced functional materials
SN - 1616-301X
IS - 5
M1 - 2302626
ER -