Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/171823
Title: Bidirectional catalyst with robust lithiophilicity and sulfiphilicity for advanced lithium–sulfur battery
Authors: Li, Yanan
Deng, Yirui
Yang, Jin-Lin
Tang, Wenhao
Ge, Ben
Liu, Ruiping
Keywords: Engineering::Chemical engineering
Issue Date: 2023
Source: Li, Y., Deng, Y., Yang, J., Tang, W., Ge, B. & Liu, R. (2023). Bidirectional catalyst with robust lithiophilicity and sulfiphilicity for advanced lithium–sulfur battery. Advanced Functional Materials, 33(44), 2302267-. https://dx.doi.org/10.1002/adfm.202302267
Journal: Advanced Functional Materials
Abstract: The application of lithium–sulfur batteries (LSBs) is immensely impeded by notorious shuttle effect, sluggish redox kinetics, and irregular Li2S deposition, which result in large polarization and rapid capacity decay. To obtain the LSBs with high energy density and fast reaction kinetics, herein, a heterostructure composed by nitrogen-deficient graphitic carbon nitride (ND-g-C3N4) and MgNCN is fabricated via a magnesiothermic denitriding technology. Lithophilic C3N4 with abundant nitrogen-deficient acts as a conductive framework, together with the sulfiphilic MgNCN, lithium-polysulfides (LiPSs) can be effectively captured followed by a regulated Li2S nucleation. Furthermore, the oxidation conversion kinetics can be accelerated as well. As expected, the LSBs with catalytic MgNCN/ND-g-C3N4 as the interlayer exhibit remarkable electrochemical performance with a discharge capacity of 650 mAh g−1 at 4 C. Meanwhile, a low capacity decay of 0.008% per cycle can be reached at 1 C after 400 cycles. Even with a high areal sulfur loading of 5.1 mg cm−2, outstanding capacity retention can be achieved at 0.5 C (64.18%) and 1 C (90.46%). The presented strategy unlocks a new way for the LSBs design with highly efficient catalyst.
URI: https://hdl.handle.net/10356/171823
ISSN: 1616-301X
DOI: 10.1002/adfm.202302267
Schools: School of Physical and Mathematical Sciences 
Rights: © 2023 Wiley-VCH GmbH. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SPMS Journal Articles

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