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学者姓名:张久俊

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Performance enhancement from catalysts to membrane electrode assemblies for high-temperature proton exchange membrane fuel cells SCIE
期刊论文 | 2025 , 139 | NANO ENERGY
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Abstract :

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) show broad application perspectives due to their faster reaction kinetics and tolerance to fuel/gas impurities as well as the easy water/heat managements. However, the catalysts and subsequent membrane electrode assemblies (MEAs) are still suffering from performance degradation, which severely restricts HT-PEMFCs' large-scale practical application. To overcome the challenges, developing high-performance catalysts and MEAs with advanced materials and optimized structures to achieve stable and efficient operation of HT-PEMFCs is necessary. To facilitate the research and development of HT-PEMFCs, a comprehensive overview of the latest developments in the design of active and stable catalysts and durable MEAs is presented in this paper. This review systematically summarizes the degradation mechanisms of catalysts, and corresponding mitigation strategies for improving the stability of catalysts and MEAs, aiming to effectively developing high-performance and durable HT-PEMFCs. Furthermore, the main challenges are analyzed and the future research directions for overcoming the challenges are also proposed for developing highactive and stable catalysts and MEAs used in HT-PEMFCs toward practical applications.

Keyword :

Catalysts Catalysts Degradation mechanisms Degradation mechanisms High-temperature proton exchange membrane fuel cells High-temperature proton exchange membrane fuel cells Membrane electrode assemblies Membrane electrode assemblies Mitigation strategies Mitigation strategies

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GB/T 7714 Xu, Chenhui , Wang, Shufan , Zheng, Yun et al. Performance enhancement from catalysts to membrane electrode assemblies for high-temperature proton exchange membrane fuel cells [J]. | NANO ENERGY , 2025 , 139 .
MLA Xu, Chenhui et al. "Performance enhancement from catalysts to membrane electrode assemblies for high-temperature proton exchange membrane fuel cells" . | NANO ENERGY 139 (2025) .
APA Xu, Chenhui , Wang, Shufan , Zheng, Yun , Liu, Haishan , Li, Lingfei , Zhuang, Zewen et al. Performance enhancement from catalysts to membrane electrode assemblies for high-temperature proton exchange membrane fuel cells . | NANO ENERGY , 2025 , 139 .
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Atomically dispersed iron-zinc dual-metal sites to boost catalytic oxygen reduction activities for efficient zinc-air batteries SCIE
期刊论文 | 2025 , 17 (15) , 9515-9524 | NANOSCALE
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Developing asymmetric heteronuclear dual-atom catalysts (DACs) through coordination microenvironment regulation and investigating their structure-activity relationship for the catalytic oxygen reduction reaction (ORR) are crucial for energy conversion and storage devices such as zinc-air batteries (ZABs). In this work, a novel catalyst with its Fe and Zn diatomic sites atomically dispersed on nitrogen-doped hierarchical porous carbon (FeZn-NC-800) was designed and synthesized under a cyanamide-assisted sintering atmosphere to stabilize Zn single atoms in the structure. Benefiting from specific synergy between the Fe and Zn atoms and the hierarchical porous carbon substrate, the obtained FeZn-NC-800 catalyst exhibits remarkable ORR performance with a positive half-wave potential of 0.89 V and good durability, outstripping the performance of most state-of-the-art catalysts and commercial precious metal catalysts. Moreover, the ZABs assembled with the FeZn-NC-800 cathodes exhibit an excellent peak power density of 218.6 mW cm-2 and achieve stable cycling for over 200 hours at a current density of 10 mA cm-2. This study provides a fresh new insight into the development of stable and highly active DAC materials, advancing the design of next-generation energy technologies.

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GB/T 7714 Zhao, Zi-Han , Ma, Dakai , Zhuang, Zewen et al. Atomically dispersed iron-zinc dual-metal sites to boost catalytic oxygen reduction activities for efficient zinc-air batteries [J]. | NANOSCALE , 2025 , 17 (15) : 9515-9524 .
MLA Zhao, Zi-Han et al. "Atomically dispersed iron-zinc dual-metal sites to boost catalytic oxygen reduction activities for efficient zinc-air batteries" . | NANOSCALE 17 . 15 (2025) : 9515-9524 .
APA Zhao, Zi-Han , Ma, Dakai , Zhuang, Zewen , Wang, Kaili , Xu, Chenhui , Sun, Kaian et al. Atomically dispersed iron-zinc dual-metal sites to boost catalytic oxygen reduction activities for efficient zinc-air batteries . | NANOSCALE , 2025 , 17 (15) , 9515-9524 .
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Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering SCIE
期刊论文 | 2025 | INTERNATIONAL JOURNAL OF GREEN ENERGY
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Cobalt and iron selenides-based materials with high theoretical capacities, low toxicity and abundant sources have been identified as the promising anode materials for sodium-ion batteries (SIBs). However, they still face the challenges of high volume expansion and slow electrode kinetics, resulting in poor rate performance and fast capacity fading. In this paper, three-dimensional honeycomb-like Co-Fe based selenide composites with different molar ratios are successfully synthesized by one-pot solvothermal, annealing and selenization processes (expressed as Co-FeSe2@C/CNs-fbs, Co-FeSe2@C/CNs-irs and Co-FeSe2@C/CNs-sbs). Benefitted from the design of three-dimensional porous compositing structure, the optimized Co-FeSe2@C/CNs-fbs electrode material possesses more active sites and structural stability, resulting in stable cycling performance and fast electron/ion transport. As a result, Co-FeSe2@C/CNs-fbs anode shows excellent rate capability (353.1 mAh g-1 at 120 A g-1) and long cycling performance (95.7% of capacity retention after 3700 cycles at 60 A g-1), surpassing most previously reported anode materials for SIBs. Meanwhile, a full-cell made up with Na3V2(PO4)3/C cathode and Co-FeSe2@C/CNs-fbs anode shows a high energy density (180.1 Wh kg-1 at a power density 630.5 W kg-1) and capacity retention rate. This study provides a feasible strategy to fabricate selenide-based composites as the anode materials for high-performance SIBs via doping and structure engineering.

Keyword :

Anode materials Anode materials co doping co doping sodium-ion batteries sodium-ion batteries three-dimensional porous structure three-dimensional porous structure transition metal selenides transition metal selenides

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GB/T 7714 Ma, Dakai , Qiu, Ruoxue , Zheng, Hui et al. Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering [J]. | INTERNATIONAL JOURNAL OF GREEN ENERGY , 2025 .
MLA Ma, Dakai et al. "Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering" . | INTERNATIONAL JOURNAL OF GREEN ENERGY (2025) .
APA Ma, Dakai , Qiu, Ruoxue , Zheng, Hui , Luo, Yiyuan , Wang, Kaili , Cai, Junming et al. Highly stable cobalt-doped FeSe2 anodes for unexpectedly fast sodium storage enabled by doping and structure engineering . | INTERNATIONAL JOURNAL OF GREEN ENERGY , 2025 .
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Surface electron reconfiguration of ceric dioxide artificial interface layer by cationic doping for dendrite-free zinc anode SCIE
期刊论文 | 2025 | FRONTIERS IN ENERGY
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Aqueous zinc metal batteries (ZMBs) are regarded as strong contenders in secondary battery systems due to their high safety and abundant resources. However, the cycling performance of the Zn anode and the overall performance of the cells have often been hindered by the formation of Zn dendrites and the occurrence of parasitic side reactions. In this paper, a surface electron reconfiguration strategy is proposed to optimize the adsorption energy and migration energy of Zn2+ for a better Zn2+ deposition/stripping process by adjusting the electronic structure of ceric dioxide (CeO2) artificial interface layer with copper atoms (Cu) doped. Both experimental results and theoretical calculations demonstrate that the Cu2Ce7Ox interface facilitates rapid transport of Zn2+ due to the optimized electronic structure and appropriate electron density, leading to a highly reversible and stable Zn anode. Consequently, the Cu2Ce7Ox@Zn symmetric cell exhibits an overpotential of only 24 mV after stably cycling for over 1600 h at a current density of 1 mA/cm2 and a capacity of 1 mAh/cm2. Additionally, the cycle life of Cu/Zn asymmetric cells exceeds 2500 h, with an average Coulombic efficiency of 99.9%. This paper provides a novel approach to the artificial interface layer strategy, offering new insights for improving the performance of ZMBs.

Keyword :

Cu2Ce7Ox Cu2Ce7Ox electronic structure electronic structure interface layer interface layer solvation structure solvation structure Zn metal batteries Zn metal batteries

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GB/T 7714 Lu, Linlong , Wang, Zheng , Cai, Jingwen et al. Surface electron reconfiguration of ceric dioxide artificial interface layer by cationic doping for dendrite-free zinc anode [J]. | FRONTIERS IN ENERGY , 2025 .
MLA Lu, Linlong et al. "Surface electron reconfiguration of ceric dioxide artificial interface layer by cationic doping for dendrite-free zinc anode" . | FRONTIERS IN ENERGY (2025) .
APA Lu, Linlong , Wang, Zheng , Cai, Jingwen , Bao, Zhengyu , Lan, Yukai , Zuo, Yinze et al. Surface electron reconfiguration of ceric dioxide artificial interface layer by cationic doping for dendrite-free zinc anode . | FRONTIERS IN ENERGY , 2025 .
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Advanced direct recycling technology enables a second life of spent lithium-ion battery SCIE
期刊论文 | 2025 , 74 | ENERGY STORAGE MATERIALS
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With the emergence of the energy crisis and the rise of human environmental awareness, lithium-ion batteries (LIBs), as a new type of energy storage device, are widely used in electric vehicles (EVs), mobile electronic products and stationary energy storage devices. The demand for LIBs has dramatically increased in recent years, leading to a shortage of raw materials for LIBs and a large number of retired LIBs. Therefore, it is particularly important to recycle spent LIBs. Compared with pyrometallurgy and hydrometallurgy, direct recycling, as a more advanced technology, focuses on repairing of the electrodes of spent LIBs. However, direct recycling technology is still in the laboratory operation stage, and there are still many difficulties and challenges to overcome. Herein, we firstly highlight the importance of recycling spent LIBs from LIB market development, raw material supply, environmental impact, and economic benefits. Subsequently, starting from the failure forms and mechanisms of electrode materials, we provide a detailed summary of various direct recycling and upcycling processes, reaction principles, as well as advantages and disadvantages. Additionally, the technology for converting waste cathodes and graphite into new functional materials, a topic rarely addressed in previous reviews, is comprehensively detailed in this review. Lastly, we provide a summary of the current status of LIB recycling and present future challenges. This review may serve as a source of inspiration for researchers and enterprises to develop more advanced recycling methodologies.

Keyword :

Direct recycling Direct recycling Electrode materials Electrode materials Failure mechanisms Failure mechanisms Spent lithium ion batteries Spent lithium ion batteries

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GB/T 7714 Shen, Ji , Zhou, Miaomiao , Liu, Wei et al. Advanced direct recycling technology enables a second life of spent lithium-ion battery [J]. | ENERGY STORAGE MATERIALS , 2025 , 74 .
MLA Shen, Ji et al. "Advanced direct recycling technology enables a second life of spent lithium-ion battery" . | ENERGY STORAGE MATERIALS 74 (2025) .
APA Shen, Ji , Zhou, Miaomiao , Liu, Wei , Shi, Yiliang , Tang, Wenhao , Deng, Yirui et al. Advanced direct recycling technology enables a second life of spent lithium-ion battery . | ENERGY STORAGE MATERIALS , 2025 , 74 .
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Green Synthesis of Cu3P to Achieve Low-Temperature and High Initial Coulombic Efficiency Sodium Ion Storage SCIE
期刊论文 | 2025 | ADVANCED ENERGY MATERIALS
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Conversion-type transition metal phosphides (TMPs) are competitive anode materials to overcome the volumetric energy density limits of hard carbon for sodium-ion batteries (SIBs). However, the application of TMPs is generally constrained by their low initial coulombic efficiency (ICE), unsatisfied cycling stability and poor low-temperature (LT) performance. Herein, a green synthesis method is reported to prepare carbon quantum dots modified Cu3P nanoparticles anchored on carbon fibers (CF@Cu3P-CQDs) as anode for high-energy and LT SIBs. It is disclosed that such a structure enables good interface contact between electrodes/electrolytes, thus prompting the formation of a uniformly fine solid electrolyte interphase and hence a record-high ICE of 93% with a volumetric capacity of 1343 mAhcm-3. Distribution of relaxation time analysis unveils that the rapid Na+ transfer between electrode/electrolyte interfaces and Na+ diffusion ability in CF@Cu3P-CQDs underlies the main reason for its high-rate capability (369-101 mAhg-1 @0.1-50 C) and LT performance (368/350 mAhg-1 @ 0.1C under -20/-40 degrees C). Promisingly, the CF@Cu3P-CQDs are directly used toward three cathode materials (namely P2-type Na0.78Ni0.31Mn0.67Nb0.02O2, carbon coated Na3V2(PO4)3, and low-cost Na4Fe3(PO4)2P2O7) without pre-sodiation process to assemble full-cells. This work sheds light on the fundamental understanding of electron/ion transfer kinetics of TMPs during de/sodiation and lays a foundation for the practical application of TMPs.

Keyword :

cuprous phosphide cuprous phosphide green chemistry green chemistry interface stability interface stability low temperature low temperature sodium ion battery sodium ion battery

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GB/T 7714 Liu, Yiming , Hu, Qingmin , Shi, Qinhao et al. Green Synthesis of Cu3P to Achieve Low-Temperature and High Initial Coulombic Efficiency Sodium Ion Storage [J]. | ADVANCED ENERGY MATERIALS , 2025 .
MLA Liu, Yiming et al. "Green Synthesis of Cu3P to Achieve Low-Temperature and High Initial Coulombic Efficiency Sodium Ion Storage" . | ADVANCED ENERGY MATERIALS (2025) .
APA Liu, Yiming , Hu, Qingmin , Shi, Qinhao , Zhao, Shengyu , Hu, Xinhong , Feng, Wuliang et al. Green Synthesis of Cu3P to Achieve Low-Temperature and High Initial Coulombic Efficiency Sodium Ion Storage . | ADVANCED ENERGY MATERIALS , 2025 .
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Understanding the Electron State Effect of Iron Single-Atom for Enhancing Solid-Solid Conversion Kinetics of Sulfur Cathodes SCIE
期刊论文 | 2025 | ADVANCED FUNCTIONAL MATERIALS
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Optimizing the solid-solid conversion kinetics has been challenging in lithium-sulfur batteries (LSBs). In this study, a nitrogen and boron dual-coordinated Fe single-atom catalyst (Fe-N2B2/C) was exploited by inducing boron atoms into the coordination shell to disrupt the nitrogen-only coordinated configuration (Fe-N-4/C). The intervention of boron reduced the oxidation state of Fe atoms, which increased electron density of the Fe 3d orbital and narrowed band gap between the conduction and valence bands. Furthermore, the elevated d-band center of Fe in Fe-N2B2/C raised the antibonding orbital energy, providing sites for charge transfer and polysulfide adsorption. These electronic modulations endowed Fe-N2B2/C with prominent anchoring capacity and catalytic activity. Consequently, in the ether-based electrolyte, the S@Fe-N2B2/C sulfur cathode delivered an initial capacity of 786 mAh g(-1) at 4.0 C, maintaining an impressive capacity retention of 82.7% after 200 cycles and exhibiting a sluggish capacity decay of 0.08% after 500 cycles. Simultaneously, in the all-solid-state system based on halide electrolytes (HEs), the S@Fe-N2B2/C cathode achieved a remarkable discharge capacity (1066 mAh g(-1), 0.1 C), high average Coulombic efficiency (>99%) and excellent cyclic stability (0.068%, 0.2 C). This study uncovers the origin of outstanding activity of Fe single-atom catalyst and provides a promising strategy for HEs-based all-solid-state system.

Keyword :

coordination modulation coordination modulation electron state electron state iron single-atom catalyst iron single-atom catalyst lithium-sulfur batteries lithium-sulfur batteries solid-solid conversion kinetics solid-solid conversion kinetics

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GB/T 7714 Cao, Guiqiang , Li, Xifei , Li, Mengyang et al. Understanding the Electron State Effect of Iron Single-Atom for Enhancing Solid-Solid Conversion Kinetics of Sulfur Cathodes [J]. | ADVANCED FUNCTIONAL MATERIALS , 2025 .
MLA Cao, Guiqiang et al. "Understanding the Electron State Effect of Iron Single-Atom for Enhancing Solid-Solid Conversion Kinetics of Sulfur Cathodes" . | ADVANCED FUNCTIONAL MATERIALS (2025) .
APA Cao, Guiqiang , Li, Xifei , Li, Mengyang , Yang, Xuan , Duan, Ruixian , Li, Ming et al. Understanding the Electron State Effect of Iron Single-Atom for Enhancing Solid-Solid Conversion Kinetics of Sulfur Cathodes . | ADVANCED FUNCTIONAL MATERIALS , 2025 .
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Activated d-electrons of p-block metals by reconfigured electron spin for kinetically boosting sulfur conversion of lithium-sulfur batteries SCIE
期刊论文 | 2025 , 139 | NANO ENERGY
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The use of p-block metals to accelerate the sulfur reduction reaction (SRR) in lithium-sulfur (Li-S) batteries is emerging. However, the d-electrons inertia of p-block metal endows the weak adsorption and catalytic ability for SRR, limiting catalyst design. Herein, we fabricate an asymmetrically coordinated p-block indium trisulfide by coordination engineering with P doping and sulfur vacancies (P-In2S3-x) for SRR. The unique coordination engineering induces the rearrangement of electrons in the s/p/d hybrid orbital, causing that P-In2S3-x shifts electron states from low to high spin, generating more unpaired electrons. The obtained high-spin configuration achieves that electron transition to a higher energy level to activate d-electrons of p-block metals, which enables a novel dp coupling between d orbitals of In atoms and the p orbitals of S atoms in LiPSs, improving adsorption and catalytic ability of p-block metals for SRR. Consequently, cell with P-In2S3-x achieves excellent capacity retention, with a very low decay rate (0.036 % per cycle at 5 C over 1000 cycles) and high performance at 0 degrees C (760 mAh g- 1 at 1 C). This study offers a strategy for modulation d-electrons activity p-block metals by tailoring electron spin to boost catalytic efficiency in Li-S batteries.

Keyword :

Catalytic mechanism Catalytic mechanism d -Electrons d -Electrons Electronic spin Electronic spin Lithium-sulfur batteries Lithium-sulfur batteries P -Block metals P -Block metals

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GB/T 7714 Huang, Zheng , Jiao, Xuechao , Lei, Jie et al. Activated d-electrons of p-block metals by reconfigured electron spin for kinetically boosting sulfur conversion of lithium-sulfur batteries [J]. | NANO ENERGY , 2025 , 139 .
MLA Huang, Zheng et al. "Activated d-electrons of p-block metals by reconfigured electron spin for kinetically boosting sulfur conversion of lithium-sulfur batteries" . | NANO ENERGY 139 (2025) .
APA Huang, Zheng , Jiao, Xuechao , Lei, Jie , Zuo, Yinze , Wang, Zheng , Lu, Linlong et al. Activated d-electrons of p-block metals by reconfigured electron spin for kinetically boosting sulfur conversion of lithium-sulfur batteries . | NANO ENERGY , 2025 , 139 .
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Interfacial Water Regulation for Nitrate Electroreduction to Ammonia at Ultralow Overpotentials SCIE
期刊论文 | 2025 , 37 (8) | ADVANCED MATERIALS
WoS CC Cited Count: 10
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Nitrate electroreduction is promising for achieving effluent waste-water treatment and ammonia production with respect to the global nitrogen balance. However, due to the impeded hydrogenation process, high overpotentials need to be surmounted during nitrate electroreduction, causing intensive energy consumption. Herein, a hydroxide regulation strategy is developed to optimize the interfacial H2O behavior for accelerating the hydrogenation conversion of nitrate to ammonia at ultralow overpotentials. The well-designed Ru & horbar;Ni(OH)(2) electrocatalyst shows a remarkable energy efficiency of 44.6% at +0.1 V versus RHE and a nearly 100% Faradaic efficiency for NH3 synthesis at 0 V versus RHE. In situ characterizations and theoretical calculations indicate that Ni(OH)(2) can regulate the interfacial H2O structure with a promoted H2O dissociation process and contribute to the spontaneous hydrogen spillover process for boosting NO3 (-) electroreduction to NH3 at Ru sites. Furthermore, the assembled rechargeable Zn-NO3 (-)/ethanol battery system exhibits an outstanding long-term cycling stability during the charge-discharge tests with the production of high-value-added ammonium acetate, showing great potential for simultaneously achieving nitrate removal, energy conversion, and chemical synthesis. This work can not only provide a guidance for interfacial H2O regulation in extensive hydrogenation reactions but also inspire the design of a novel hybrid flow battery with multiple functions.

Keyword :

ammonia synthesis ammonia synthesis hydrogen spillover hydrogen spillover interfacial H2O regulation interfacial H2O regulation nitrate electroreduction nitrate electroreduction rechargeable hybrid flow battery rechargeable hybrid flow battery ultralow overpotentials ultralow overpotentials

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GB/T 7714 Wan, Yuchi , Pei, Maojun , Tang, Yixiang et al. Interfacial Water Regulation for Nitrate Electroreduction to Ammonia at Ultralow Overpotentials [J]. | ADVANCED MATERIALS , 2025 , 37 (8) .
MLA Wan, Yuchi et al. "Interfacial Water Regulation for Nitrate Electroreduction to Ammonia at Ultralow Overpotentials" . | ADVANCED MATERIALS 37 . 8 (2025) .
APA Wan, Yuchi , Pei, Maojun , Tang, Yixiang , Liu, Yao , Yan, Wei , Zhang, Jiujun et al. Interfacial Water Regulation for Nitrate Electroreduction to Ammonia at Ultralow Overpotentials . | ADVANCED MATERIALS , 2025 , 37 (8) .
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Superstructure regulation and transition-metal migration suppression for highly stable Li-rich Mn-based cathode materials by anti-site Mg doping strategy SCIE
期刊论文 | 2025 , 512 | CHEMICAL ENGINEERING JOURNAL
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Li-rich layered oxides (LLOs), contributing ultrahigh discharge capacity and energy density, are considered as promising cathode candidates for Li-ion batteries. However, thermodynamically spontaneous transition metal (TM) migration and irreversible oxygen loss, which are originated from the characteristic LiMn6 ordering domains in the TM layer, usually lead to rapid capacity decline, severe voltage fading and voltage hysteresis of LLOs. Herein, distinctive MgMn6 superstructure is incorporated into the TM layers through a unique anti-site Mg2+ doping strategy to disperse the original aggregated LiMn6 superstructure and consequently solve the above issues of LLOs. Specifically, Mg2+ are pre-incorporated into the TM layers of P3-type NaTMO2, which is subsequently transformed to O3-LLOs via an ion-exchange method, instead of the traditional sintering process usually leading to Mg2+ incorporation into the Li layers. Series of in-situ/ex-situ characterizations and theoretical calculations reveal that, owing to the pinning effect of the incorporated MgMn6 superstructure, the anti-site Mg2+ doping can inherently retard the in-plane/out-plane TM migration and improve the anionic reversibility, leading to the enhanced stability of the layered structure upon cycling. Therefore, the anti-site Mg doped Li0.7[Li0.18Mg0.02Mn0.65Co0.15]O2 cathode exhibits an excellent capacity retention of 86.22 % and mitigated voltage fading of 0.40 mV per cycle after 500 cycles at 1C. These findings provide inspiring insights for superstructure design in Li-rich Mn-based cathode materials, and open up new path to develop advanced cathodes materials with reversible anionic redox chemistry.

Keyword :

Anti-site doping Anti-site doping Li-rich Mn-based cathode materials Li-rich Mn-based cathode materials Superstructure regulation Superstructure regulation Transition-metal migration Transition-metal migration Voltage stability Voltage stability

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GB/T 7714 Shen, Chao , Duan, Qiming , Li, Meng et al. Superstructure regulation and transition-metal migration suppression for highly stable Li-rich Mn-based cathode materials by anti-site Mg doping strategy [J]. | CHEMICAL ENGINEERING JOURNAL , 2025 , 512 .
MLA Shen, Chao et al. "Superstructure regulation and transition-metal migration suppression for highly stable Li-rich Mn-based cathode materials by anti-site Mg doping strategy" . | CHEMICAL ENGINEERING JOURNAL 512 (2025) .
APA Shen, Chao , Duan, Qiming , Li, Meng , Xiong, Tianyu , Fan, Zhengwei , Jiang, Yong et al. Superstructure regulation and transition-metal migration suppression for highly stable Li-rich Mn-based cathode materials by anti-site Mg doping strategy . | CHEMICAL ENGINEERING JOURNAL , 2025 , 512 .
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