Teng Li

University of Electronic Science and Technology of China

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University of Electronic Science and Technology of China

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Teng Li has a total of 63 co-authors. Here are the top co-authors by number of shared publications:

Philip Lightfoot
School of Chemistry and EaStChem, University of St Andrews, St Andrews KY16 9ST, UK
5 shared publications
Zixuan Fang
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, China
4 shared publications
Alexandra Martha Zoya Slawin
EaStCHEM School of Chemistry University of St Andrews St Andrews UK
3 shared publications
Bowen Fu
3 shared publications
Jian Yang
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu 611731, Sichuan, People’s Republic of China
3 shared publications
Mengqiang Wu
School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu, 611731, China
3 shared publications

Latest Publications

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Cited by 3
- 9 May 2024
- Published by American Chemical Society (ACS) in Chemistry of Materials
Extending the Family of Hybrid Layered Fluoride Perovskites
by Teng Li, Alasdair J. Bradford, Stephen L. Lee, Philip Lightfoot
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- 9 May 2024
- Published by American Chemical Society (ACS) in Chemistry of Materials
Open Access
Extending the Family of Hybrid Layered Fluoride Perovskites
by Teng Li, Alasdair J. Bradford, Stephen L. Lee, Philip Lightfoot
Cited by 3
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Cited by 19
- 31 July 2023
- Published by Elsevier in Ceramics International
Aliovalent dual element co-assisted strategy to enhance ionic conductivity and stability of NASICON-type solid electrolyte for all-solid-state sodium batteries
by Ziqiang Xu, Bowen Fu, Xin Hu, Jintian Wu, Teng Li, Hongyu Yang, Kashif Khan, Mengqiang Wu, Zixuan Fang
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- 31 July 2023
- Published by Elsevier in Ceramics International
Aliovalent dual element co-assisted strategy to enhance ionic conductivity and stability of NASICON-type solid electrolyte for all-solid-state sodium batteries
by Ziqiang Xu, Bowen Fu, Xin Hu, Jintian Wu, Teng Li, Hongyu Yang, Kashif Khan, Mengqiang Wu, Zixuan Fang
Cited by 19
Open Access
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Cited by 12
- 3 May 2023
- Published by American Chemical Society (ACS) in Chemistry of Materials
Manipulation of the Structure and Optoelectronic Properties through Bromine Inclusion in a Layered Lead Bromide Perovskite
by Lin-Jie Yang, Wenye Xuan, David Webster, Lethy Krishnan Jagadamma, Teng Li, David N. Miller, David B. Cordes, Alexandra M. Z. Slawin, Graham A. Turnbull, Ifor D. W. Samuel, et al.
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- 3 May 2023
- Published by American Chemical Society (ACS) in Chemistry of Materials
Open Access
Manipulation of the Structure and Optoelectronic Properties through Bromine Inclusion in a Layered Lead Bromide Perovskite
by Lin-Jie Yang, Wenye Xuan, David Webster, Lethy Krishnan Jagadamma, Teng Li, David N. Miller, David B. Cordes, Alexandra M. Z. Slawin, Graham A. Turnbull, Ifor D. W. Samuel, et al.
Cited by 12
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Cited by 6
- 1 April 2023
- Published by The Electrochemical Society in Journal of the Electrochemical Society
Enhanced Electrochemical Delithiation of LiFePO₄ in a Composite Aqueous Electrolyte for High-Performance Olivine FePO₄
by Qing Zhao, Shu Zhang, Teng Li, Caili Xu, Jian Yang, Bing Qu, Haiping Zhou, Tingting Feng, Mengqiang Wu
Development of delithiation methods with cost-efficiency and highly kinetic effectivity is of great importance for the preparation of diversified intercalation materials, mechanistic study, and lithium extraction from spent lithium-ion batteries. Electrochemical delithiation in aqueous electrolytes is low-cost, straightforward, and fast, but has been plagued by incomplete delithiation. To address this issue, we propose to add oxidation reagents, usually applied in chemical delithation, to traditional aqueous delithiation electrolyte. As a demonstration, herein, a Na₂SO₄ + Na₂S₂O₈ composite aqueous electrolyte is used to obtain olivine FePO₄ from the electrochemical delithiation of LiFePO₄, and compared with the similar delithiation in Na₂SO₄ aqueous electrolyte. The delithiation goes completion in the composite electrolyte 79% faster than that in traditional electrolyte. The resulting olivine FePO₄ exhibits integrity in terms of structure and electrochemical properties, with discharge specific capacity of 157.1 mAh g⁻¹ at 0.1 C, constant voltage plateau of 3.37 V, and 98.8% capacity retention after 100 cycles, all comparable to the LiFePO₄ starting material. Mechanistic studies show that Na₂S₂O₈ promotes the electrochemical delithiation by providing acidic and chemically oxidative conditions.
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- 1 April 2023
- Published by The Electrochemical Society in Journal of the Electrochemical Society
Enhanced Electrochemical Delithiation of LiFePO₄ in a Composite Aqueous Electrolyte for High-Performance Olivine FePO₄
by Qing Zhao, Shu Zhang, Teng Li, Caili Xu, Jian Yang, Bing Qu, Haiping Zhou, Tingting Feng, Mengqiang Wu
Development of delithiation methods with cost-efficiency and highly kinetic effectivity is of great importance for the preparation of diversified intercalation materials, mechanistic study, and lithium extraction from spent lithium-ion batteries. Electrochemical delithiation in aqueous electrolytes is low-cost, straightforward, and fast, but has been plagued by incomplete delithiation. To address this issue, we propose to add oxidation reagents, usually applied in chemical delithation, to traditional aqueous delithiation electrolyte. As a demonstration, herein, a Na₂SO₄ + Na₂S₂O₈ composite aqueous electrolyte is used to obtain olivine FePO₄ from the electrochemical delithiation of LiFePO₄, and compared with the similar delithiation in Na₂SO₄ aqueous electrolyte. The delithiation goes completion in the composite electrolyte 79% faster than that in traditional electrolyte. The resulting olivine FePO₄ exhibits integrity in terms of structure and electrochemical properties, with discharge specific capacity of 157.1 mAh g⁻¹ at 0.1 C, constant voltage plateau of 3.37 V, and 98.8% capacity retention after 100 cycles, all comparable to the LiFePO₄ starting material. Mechanistic studies show that Na₂S₂O₈ promotes the electrochemical delithiation by providing acidic and chemically oxidative conditions.
Cited by 6
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Cited by 6
- 8 March 2023
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
Nanoscale control and tri-element co-doping of 4.6 V LiCoO₂ with excellent rate capability and long-cycling stability for lithium-ion batteries
by Xun Wang, Zixuan Fang, Xin Hu, Bowen Fu, Tingting Feng, Teng Li, Mengqiang Wu
Nanosizing and tri-element co-doping synergistically enhance the electrochemical performance of LiCoO₂ at high voltage.
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- 8 March 2023
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
Nanoscale control and tri-element co-doping of 4.6 V LiCoO₂ with excellent rate capability and long-cycling stability for lithium-ion batteries
by Xun Wang, Zixuan Fang, Xin Hu, Bowen Fu, Tingting Feng, Teng Li, Mengqiang Wu
Nanosizing and tri-element co-doping synergistically enhance the electrochemical performance of LiCoO₂ at high voltage.
Cited by 6
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Cited by 25
- 13 October 2022
- Published by Elsevier in Journal of Colloid and Interface Science
Melting lithium alloying to improve the affinity of Cu foil for ultra-thin lithium metal anode
by Jian Yang, Cheng Chen, Khan Kashif, Qing Zhao, Caili Xu, Teng Li, Zixuan Fang, Mengqiang Wu
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- 13 October 2022
- Published by Elsevier in Journal of Colloid and Interface Science
Melting lithium alloying to improve the affinity of Cu foil for ultra-thin lithium metal anode
by Jian Yang, Cheng Chen, Khan Kashif, Qing Zhao, Caili Xu, Teng Li, Zixuan Fang, Mengqiang Wu
Cited by 25
Open Access
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Cited by 2
- 13 October 2022
- Published by MDPI AG in Crystals
Layered Hybrid iron Fluorides
by Teng Li, Philip Lightfoot
The first examples of layered hybrid iron fluorides are reported. In the reactions carried out, the chain compound (H₂pipz)FeF₅·H₂O always occurs as the major phase, with the layered compounds, (H₂pipz)₃Fe₄F1₈·2H₂O and (H₂pipz)₂Fe₃F₁₃·H₂O, being isolated from some reactions as major impurities. The latter two compounds feature two-dimensional sheets of corner-and edge-shared FeIIIF₆ octahedra, resulting in two distinct layer architectures. The compound (H₂pipz)FeF₅·H₂O, isolated as the major phase, crystallises with a one-dimensional structure exhibiting zig-zag [FeF₅]_∞ chains. This work opens up the potential for a much wider family of layered hybrid transition-metal fluorides.
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- 13 October 2022
- Published by MDPI AG in Crystals
Open Access
Layered Hybrid iron Fluorides
by Teng Li, Philip Lightfoot
The first examples of layered hybrid iron fluorides are reported. In the reactions carried out, the chain compound (H₂pipz)FeF₅·H₂O always occurs as the major phase, with the layered compounds, (H₂pipz)₃Fe₄F1₈·2H₂O and (H₂pipz)₂Fe₃F₁₃·H₂O, being isolated from some reactions as major impurities. The latter two compounds feature two-dimensional sheets of corner-and edge-shared FeIIIF₆ octahedra, resulting in two distinct layer architectures. The compound (H₂pipz)FeF₅·H₂O, isolated as the major phase, crystallises with a one-dimensional structure exhibiting zig-zag [FeF₅]_∞ chains. This work opens up the potential for a much wider family of layered hybrid transition-metal fluorides.
Cited by 2
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Cited by 51
- 29 September 2022
- Published by Elsevier in Ceramics International
Composite polymer electrolyte incorporating WO3 nanofillers with enhanced performance for dendrite-free solid-state lithium battery
by Kashif Khan, Bowen Fu, Hu Xin, Bayu Admasu Beshiwork, Muhammad Bilal Hanif, Jintian Wu, Zixuan Fang, Jian Yang, Teng Li, Cheng Chen, et al.
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- 29 September 2022
- Published by Elsevier in Ceramics International
Composite polymer electrolyte incorporating WO3 nanofillers with enhanced performance for dendrite-free solid-state lithium battery
by Kashif Khan, Bowen Fu, Hu Xin, Bayu Admasu Beshiwork, Muhammad Bilal Hanif, Jintian Wu, Zixuan Fang, Jian Yang, Teng Li, Cheng Chen, et al.
Cited by 51
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Cited by 14
- 23 October 2020
- Published by American Physical Society (APS) in Physical Review Materials
Realizing square and diamond lattice $S = 1 / 2$ Heisenberg antiferromagnet models in the $α$ and $β$ phases of the coordination framework, $K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$
by Aly H. Abdeldaim, Teng Li, Lewis Farrar, Alexander A. Tsirlin, Wenjiao Yao, Alexandra S. Gibbs, Pascal Manuel, Philip Lightfoot, Gøran J. Nilsen, Lucy Clark
We report the crystal structures and magnetic properties of two pseudopolymorphs of the $S = 1 / 2 {Ti}^{3 +}$ coordination framework, $K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ . Single-crystal x-ray and powder neutron diffraction measurements on $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ confirm its structure in the tetragonal $I 4 / m c m$ space group with a square planar arrangement of ${Ti}^{3 +}$ ions. Magnetometry and specific heat measurements reveal weak antiferromagnetic interactions, with $J_{1} \approx 7$ K and $J_{2} / J_{1} = 0.11$ indicating a slight frustration of nearest- and next-nearest-neighbor interactions. Below 1.8 K, $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ undergoes a transition to G-type antiferromagnetic order with magnetic moments aligned along the $c$ axis of the tetragonal structure. The estimated ordered moment of ${Ti}^{3 +}$ in $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ is suppressed from its spin-only value to $0.62 (3) μ_{B}$ , thus verifying the two-dimensional nature of the magnetic interactions within the system. $β - K Ti {(C_{2} O_{4})}_{2} \cdot 2 H_{2} O$ , on the other hand, realizes a three-dimensional diamondlike magnetic network of ${Ti}^{3 +}$ moments within a hexagonal $P 6_{2} 22$ structure. An antiferromagnetic exchange coupling of $J \approx 54$ K—an order of magnitude larger than in $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ —is extracted from magnetometry and specific heat data. $β - K Ti {(C_{2} O_{4})}_{2} \cdot 2 H_{2} O$ undergoes Néel ordering at $T_{N} = 28$ K, with the magnetic moments aligned within the $a b$ plane and a slightly reduced ordered moment of $0.79 μ_{B}$ per ${Ti}^{3 +}$ . Through density-functional theory calculations, we address the origin of the large difference in the exchange parameters between the $α$ and $β$ pseudopolymorphs. Given their observed magnetic behaviors, we propose $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ and $β - K Ti {(C_{2} O_{4})}_{2} \cdot 2 H_{2} O$ as close to ideal model $S = 1 / 2$ Heisenberg square and diamond lattice antiferromagnets, respectively.
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- 23 October 2020
- Published by American Physical Society (APS) in Physical Review Materials
Realizing square and diamond lattice $S = 1 / 2$ Heisenberg antiferromagnet models in the $α$ and $β$ phases of the coordination framework, $K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$
by Aly H. Abdeldaim, Teng Li, Lewis Farrar, Alexander A. Tsirlin, Wenjiao Yao, Alexandra S. Gibbs, Pascal Manuel, Philip Lightfoot, Gøran J. Nilsen, Lucy Clark
We report the crystal structures and magnetic properties of two pseudopolymorphs of the $S = 1 / 2 {Ti}^{3 +}$ coordination framework, $K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ . Single-crystal x-ray and powder neutron diffraction measurements on $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ confirm its structure in the tetragonal $I 4 / m c m$ space group with a square planar arrangement of ${Ti}^{3 +}$ ions. Magnetometry and specific heat measurements reveal weak antiferromagnetic interactions, with $J_{1} \approx 7$ K and $J_{2} / J_{1} = 0.11$ indicating a slight frustration of nearest- and next-nearest-neighbor interactions. Below 1.8 K, $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ undergoes a transition to G-type antiferromagnetic order with magnetic moments aligned along the $c$ axis of the tetragonal structure. The estimated ordered moment of ${Ti}^{3 +}$ in $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ is suppressed from its spin-only value to $0.62 (3) μ_{B}$ , thus verifying the two-dimensional nature of the magnetic interactions within the system. $β - K Ti {(C_{2} O_{4})}_{2} \cdot 2 H_{2} O$ , on the other hand, realizes a three-dimensional diamondlike magnetic network of ${Ti}^{3 +}$ moments within a hexagonal $P 6_{2} 22$ structure. An antiferromagnetic exchange coupling of $J \approx 54$ K—an order of magnitude larger than in $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ —is extracted from magnetometry and specific heat data. $β - K Ti {(C_{2} O_{4})}_{2} \cdot 2 H_{2} O$ undergoes Néel ordering at $T_{N} = 28$ K, with the magnetic moments aligned within the $a b$ plane and a slightly reduced ordered moment of $0.79 μ_{B}$ per ${Ti}^{3 +}$ . Through density-functional theory calculations, we address the origin of the large difference in the exchange parameters between the $α$ and $β$ pseudopolymorphs. Given their observed magnetic behaviors, we propose $α - K Ti {(C_{2} O_{4})}_{2} \cdot x H_{2} O$ and $β - K Ti {(C_{2} O_{4})}_{2} \cdot 2 H_{2} O$ as close to ideal model $S = 1 / 2$ Heisenberg square and diamond lattice antiferromagnets, respectively.
Cited by 14
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Cited by 11
- 26 February 2019
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
A hybrid fluoride layered perovskite, (enH₂)MnF₄
by Teng Li, Rebecca Clulow, Alasdair J. Bradford, Stephen L. Lee, Alexandra M. Z. Slawin, Philip Lightfoot
The title compound represents the first example of a hybrid layered fluoride perovskite.
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- 26 February 2019
- Published by Royal Society of Chemistry (RSC) in Dalton Transactions
A hybrid fluoride layered perovskite, (enH₂)MnF₄
by Teng Li, Rebecca Clulow, Alasdair J. Bradford, Stephen L. Lee, Alexandra M. Z. Slawin, Philip Lightfoot
The title compound represents the first example of a hybrid layered fluoride perovskite.
Cited by 11

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