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学者姓名：汪浩
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摘要 ：
Zinc-air batteries (ZABs) are regarded as attractive devices for electrochemical energy storage and conversion due to their outstanding electrochemical performance, low price, and high safety. However, it remains a chal-lenge to design a stable and efficient bifunctional oxygen catalyst that can accelerate the reaction kinetics and improve the performance of ZABs. Herein, a phosphorus-doped transition metal selenide/carbon com-posite catalyst derived from metal-organic frameworks (P-CoSe2/C@CC) is constructed by a self-supporting carbon cloth structure through a simple solvothermal process with subsequent selenization and phosphati-zation. The P-CoSe2/C@CC exhibits a low overpotential of 303.1 mV at 10 mA cm-2 toward the oxygen evo-lution reaction and an obvious reduction peak for the oxygen reduction reaction. The abovementioned electrochemical performances for the P-CoSe2/C@CC are attributed to the specific architecture, the super-hydrophilic surface, and the P-doping effect. Remarkably, the homemade zinc-air battery based on our P-CoSe2/C@CC catalyst shows an expected peak power density of 124.4 mW cm-2 along with excellent cycling stability, confirming its great potential application in ZABs for advanced bifunctional electrocatalysis.(c) 2022 Elsevier Inc. All rights reserved.
关键词 ：
Zinc-air battery Zinc-air battery Phosphorus doping Phosphorus doping Bifunctional oxygen catalyst Bifunctional oxygen catalyst Metal-organic frameworks Metal-organic frameworks Cobalt selenide Cobalt selenide
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| GB/T 7714 | Mi, Hongtian , Li, Leyuan , Zeng, Chuitao et al. Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries [J]. | JOURNAL OF COLLOID AND INTERFACE SCIENCE , 2023 , 633 : 424-431 . |
| MLA | Mi, Hongtian et al. "Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries" . | JOURNAL OF COLLOID AND INTERFACE SCIENCE 633 (2023) : 424-431 . |
| APA | Mi, Hongtian , Li, Leyuan , Zeng, Chuitao , Jin, Yuhong , Zhang, Qianqian , Zhou, Kailing et al. Cuboid-like phosphorus-doped metal-organic framework-derived CoSe2 on carbon cloth as an advanced bifunctional oxygen electrocatalyst for rechargeable zinc-air batteries . | JOURNAL OF COLLOID AND INTERFACE SCIENCE , 2023 , 633 , 424-431 . |
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摘要 ：
Transition metal phosphides with a satisfying theoretical electrochemical characteristics are the promising environmentally friendly energy storage materials for high-performance electrochemical capacitors. The possession of high specific surface area, numerous active sites and stable structure is helpful for the electrochemical energy storage process. In this study, porous hierarchical Ni2P nanosheet arrays combined with Cu3P layers on copper foam (Ni2P/C@Cu3P-CF) is fabricated via hydrothermal-reduction/carbonization-phosphorization process using the 2D Ni-based metal organic framework nanosheets as the precursor. Benefit from this rational design and super-hydrophilic property, the Ni2P/C@Cu3P-CF electrode possess a satisfying capacity of 1105.0 mC cm(-2) at a current density of 5 mA cm(-2) and good rate performance (61.5% capacity retention at a high current density of 50 mA cm(-2)). In addition, asymmetrical all-solid-state electrochemical capacitors assembled with our Ni2P/C@Cu3P-CF electrode can deliver a high areal energy density of 1.6 mWh cm(-2 )at a power density of 0.16 mW cm(-2). Moreover, this electrochemical capacitors display the robust cycling stability with a 91.2% capacity retention after 5000 cycles at a rate of 10 mA cm(-2). These results demonstrate a great potential for the Ni2P/C@Cu3P-CF electrode in the commercial application of the advanced aqueous electrochemical energy storage device.
关键词 ：
Asymmetrical electrochemical capacitors Asymmetrical electrochemical capacitors Cu 3 P layer Cu 3 P layer Ni2P nanosheet Ni2P nanosheet Ni-MOF Ni-MOF High areal capacitance High areal capacitance
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| GB/T 7714 | Li, Leyuan , Jin, Yuhong , Zeng, Chuitao et al. Porous hierarchical Ni2P nanosheet arrays combined with Cu3P layers on copper foam as a binder-free battery-type cathode for high-energy-density asymmetrical all-solid-state electrochemical capacitors [J]. | JOURNAL OF ENERGY STORAGE , 2022 , 52 . |
| MLA | Li, Leyuan et al. "Porous hierarchical Ni2P nanosheet arrays combined with Cu3P layers on copper foam as a binder-free battery-type cathode for high-energy-density asymmetrical all-solid-state electrochemical capacitors" . | JOURNAL OF ENERGY STORAGE 52 (2022) . |
| APA | Li, Leyuan , Jin, Yuhong , Zeng, Chuitao , Ren, Dayong , Zhou, Kailing , Zhang, Qianqian et al. Porous hierarchical Ni2P nanosheet arrays combined with Cu3P layers on copper foam as a binder-free battery-type cathode for high-energy-density asymmetrical all-solid-state electrochemical capacitors . | JOURNAL OF ENERGY STORAGE , 2022 , 52 . |
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摘要 ：
Electrochromic energy storage devices (EESDs) integrate energy storage and electrochromism into one smart device that can realize the visualization of the energy level by the naked eyes, which has attracted extensive attention in recent years. It is critical to explore suitable electrode materials for achieving both high electrochromic and electrochemical performance. Herein, we propose an aqueous aluminum-ion electrochromic energy storage device (AIEESD) by assembling the polyaniline (PANI) electrochromic cathode, Al metal frame anode and AlCl3 electrolyte, which yields an open-circuit voltage of similar to 1.22 V and a fast self-bleaching behavior without any energy input. Additionally, the developed device exhibits outstanding electrochromic energy storage performances with discharging capacity of 68.1 mAh m(-2), excellent rate capability, large optical modulation (Delta T = 55% at 630 nm) and high coloration efficiency (93.62 cm(2) C-1 at 630 nm). Moreover, the prototype device can reversibly switch between the multicolor (transparent, light yellow, green and dark blue) when the voltage changes from 0.4 to 2.5 V, which means the energy status can be monitored by the obvious color transition. These results show that the AIEESD in this work has great application prospects for smart windows and energy storage displays.
关键词 ：
Electrochromic Electrochromic Energy storage Energy storage Polyaniline Polyaniline Self-bleaching Self-bleaching
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| GB/T 7714 | Gong, Hui , Wang, Shuyi , Xie, Ming et al. An aqueous aluminum-ion electrochromic energy storage device with visual energy level [J]. | SOLAR ENERGY MATERIALS AND SOLAR CELLS , 2022 , 248 . |
| MLA | Gong, Hui et al. "An aqueous aluminum-ion electrochromic energy storage device with visual energy level" . | SOLAR ENERGY MATERIALS AND SOLAR CELLS 248 (2022) . |
| APA | Gong, Hui , Wang, Shuyi , Xie, Ming , Wang, Hao . An aqueous aluminum-ion electrochromic energy storage device with visual energy level . | SOLAR ENERGY MATERIALS AND SOLAR CELLS , 2022 , 248 . |
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摘要 ：
Electrochemical water splitting is the most direct and popular method to obtain hydrogen. However, the high activation barrier for water splitting greatly hinders large-scale hydrogen production, inspiring the necessity of using catalysts for the hydrogen evolution reaction and oxygen evolution reaction. Materials from precious metals to earth-abundant transition metals and their composites have been widely developed, in which transition metal selenides display a more outstanding bifunctional catalytic performance. This review aims to focus on the design strategies of transition metal selenide based catalysts from modification methods, including morphological control, anion substitution and cation substitution, as well as using composite materials modified by constructing heterostructures and the synergistic effect of different components. Finally, it provides guidance for the research status, and future development directions of multifunctional electrocatalytic selenide based materials are also suggested.
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| GB/T 7714 | Zeng, ChuiTao , Dai, Lingyun , Jin, YuHong et al. Design strategies toward transition metal selenide-based catalysts for electrochemical water splitting [J]. | SUSTAINABLE ENERGY & FUELS , 2021 , 5 (5) : 1347-1365 . |
| MLA | Zeng, ChuiTao et al. "Design strategies toward transition metal selenide-based catalysts for electrochemical water splitting" . | SUSTAINABLE ENERGY & FUELS 5 . 5 (2021) : 1347-1365 . |
| APA | Zeng, ChuiTao , Dai, Lingyun , Jin, YuHong , Liu, JingBing , Zhang, QianQian , Wang, Hao . Design strategies toward transition metal selenide-based catalysts for electrochemical water splitting . | SUSTAINABLE ENERGY & FUELS , 2021 , 5 (5) , 1347-1365 . |
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摘要 ：
Single-atom catalysts provide an effective approach to reduce the amount of precious metals meanwhile maintain their catalytic activity. However, the sluggish activity of the catalysts for alkaline water dissociation has hampered advances in highly efficient hydrogen production. Herein, we develop a single-atom platinum immobilized NiO/Ni heterostructure (Pt-SA-NiO/Ni) as an alkaline hydrogen evolution catalyst. It is found that Pt single atom coupled with NiO/Ni heterostructure enables the tunable binding abilities of hydroxyl ions (OH*) and hydrogen (H*), which efficiently tailors the water dissociation energy and promotes the H* conversion for accelerating alkaline hydrogen evolution reaction. A further enhancement is achieved by constructing Pt-SA-NiO/Ni nanosheets on Ag nanowires to form a hierarchical three-dimensional morphology. Consequently, the fabricated Pt-SA-NiO/Ni catalyst displays high alkaline hydrogen evolution performances with a quite high mass activity of 20.6Amg(-1) for Pt at the overpotential of 100mV, significantly outperforming the reported catalysts. While H-2 evolution from water may represent a renewable energy source, there is a strong need to improve catalytic efficiencies while maximizing materials utilization. Here, authors examine single-atom Pt on nickel-based heterostructures as highly active electrocatalysts for alkaline H-2 evolution.
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| GB/T 7714 | Zhou, Kai Ling , Wang, Zelin , Han, Chang Bao et al. Platinum single-atom catalyst coupled with transition metal/metal oxide heterostructure for accelerating alkaline hydrogen evolution reaction [J]. | NATURE COMMUNICATIONS , 2021 , 12 (1) . |
| MLA | Zhou, Kai Ling et al. "Platinum single-atom catalyst coupled with transition metal/metal oxide heterostructure for accelerating alkaline hydrogen evolution reaction" . | NATURE COMMUNICATIONS 12 . 1 (2021) . |
| APA | Zhou, Kai Ling , Wang, Zelin , Han, Chang Bao , Ke, Xiaoxing , Wang, Changhao , Jin, Yuhong et al. Platinum single-atom catalyst coupled with transition metal/metal oxide heterostructure for accelerating alkaline hydrogen evolution reaction . | NATURE COMMUNICATIONS , 2021 , 12 (1) . |
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摘要 ：
Developing high energy density lithium secondary batteries is pivotal for satisfying the increasing demand in advanced energy storage systems. Lithium metal batteries (LMBs) have attracted growing attention due to their high theoretical capacity, but the lithium dendrites issue severely fetter their real-world applications. It is found that reducing anion migration near lithium metal prolongs the nucleation time of dendrites, meanwhile, promoting homogeneous lithium deposition suppresses the dendritic growth. Thus, regulating ion transport in LMBs is a feasible and effective strategy for addressing the issues. Based on this, a functional separator is developed to regulate ion transport by utilizing a well-designed metal-organic frameworks (MOFs) coating to functionalize polypropylene (PP) separator. The well-defined intrinsic nanochannels in MOFs and the negatively charged gap channels both restricts the free migration of anions, contributing to a high Li+ transference number of 0.68. Meanwhile, the MOFs coating with uniform porous structure promotes homogeneous lithium deposition. Consequently, a highly-stable Li plating/stripping cycling for over 150 h is achieved. Furthermore, implementation of the separator enables LMBs with high discharge capacity, prominent rate performance and good capacity retention. This work is anticipated to aid developement of dendrite-free LMBs by utilizing advanced separators with ion transport management.
关键词 ：
functional separators functional separators lithium dendrites lithium dendrites lithium metal anodes lithium metal anodes metal-organic frameworks metal-organic frameworks nanochannels nanochannels
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| GB/T 7714 | Hao, Zhendong , Wu, Yue , Zhao, Qing et al. Functional Separators Regulating Ion Transport Enabled by Metal-Organic Frameworks for Dendrite-Free Lithium Metal Anodes [J]. | ADVANCED FUNCTIONAL MATERIALS , 2021 , 31 (33) . |
| MLA | Hao, Zhendong et al. "Functional Separators Regulating Ion Transport Enabled by Metal-Organic Frameworks for Dendrite-Free Lithium Metal Anodes" . | ADVANCED FUNCTIONAL MATERIALS 31 . 33 (2021) . |
| APA | Hao, Zhendong , Wu, Yue , Zhao, Qing , Tang, Jiadong , Zhang, Qianqian , Ke, Xiaoxing et al. Functional Separators Regulating Ion Transport Enabled by Metal-Organic Frameworks for Dendrite-Free Lithium Metal Anodes . | ADVANCED FUNCTIONAL MATERIALS , 2021 , 31 (33) . |
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摘要 ：
Layered ternary lithium-ion batteries LiNixCoyMnzO2 (NCM) and LiNixCoyAlzO2 (NCA) have become mainstream power batteries due to their large specific capacity, low cost, and high energy density. However, these layered ternary lithium-ion batteries still have electrochemical cycling problems such as rapid capacity decline and poor thermal stability. These problems are mainly caused by (1) irreversible phase transition, (2) crack and pulverization of cathode electrode material particles, (3) dissolution of transition metal elements, (4) oxidative decomposition of electrolyte and (5) repeated growth and thickening of the SEI film on the anode electrode. In order to solve these problems, various strategies based on doping and coating of the cathode material, design of electrolyte, and anode coating have been studied to effectively stabilize the NCM/NCA cathode and achieve the purpose of improving its electrochemical cycling performance. This review briefly describes the working principle of lithium-ion batteries, the composition and structure of NCM/NCA cathode materials and the roles of transition metal elements. The capacity degradation mechanism of layered ternary lithium-ion batteries is reviewed from the perspectives of cathode, electrolyte and anode, and the research progress in the modification of cathode materials is emphatically discussed. Advances in the modification of anode materials and electrolyte design are also briefly introduced. Finally, some challenges and prospects are proposed for the future development of layered ternary lithium-ion batteries.
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| GB/T 7714 | Zhang, JianHua , Jin, YuHong , Liu, JingBing et al. Recent advances in understanding and relieving capacity decay of lithium ion batteries with layered ternary cathodes [J]. | SUSTAINABLE ENERGY & FUELS , 2021 , 5 (20) : 5114-5138 . |
| MLA | Zhang, JianHua et al. "Recent advances in understanding and relieving capacity decay of lithium ion batteries with layered ternary cathodes" . | SUSTAINABLE ENERGY & FUELS 5 . 20 (2021) : 5114-5138 . |
| APA | Zhang, JianHua , Jin, YuHong , Liu, JingBing , Zhang, QianQian , Wang, Hao . Recent advances in understanding and relieving capacity decay of lithium ion batteries with layered ternary cathodes . | SUSTAINABLE ENERGY & FUELS , 2021 , 5 (20) , 5114-5138 . |
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摘要 ：
The selective transport of charge carriers has a great impact on the efficiency of electrochemical energy storage and conversion. However, pursuing membranes with high-performance ion selectivity is one of the most crucial issues for their further progress. In recent years, based on their superior intrinsically physical and chemical properties including abundant nano-sized channels, open metal sites and electrostatic interaction, metal-organic frameworks (MOFs) have shown enormous potential for the construction of membranes with ion selectivity. In this review, the design and mechanism of MOF-based membranes with ion selectivity are first discussed. Based on this, the applications of these membranes in typical electrochemical energy storage and conversion systems are summarized. Based on the recent advances, the existing challenges and the future perspectives are discussed. This review will offer new insights for understanding the ion transport in MOF-based membranes with ion selectivity towards high-performance electrochemical energy storage and conversion.
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| GB/T 7714 | Hao, Zhendong , Wu, Yue , Hu, Yating et al. Advanced metal-organic framework-based membranes with ion selectivity for boosting electrochemical energy storage and conversion [J]. | JOURNAL OF MATERIALS CHEMISTRY A , 2021 . |
| MLA | Hao, Zhendong et al. "Advanced metal-organic framework-based membranes with ion selectivity for boosting electrochemical energy storage and conversion" . | JOURNAL OF MATERIALS CHEMISTRY A (2021) . |
| APA | Hao, Zhendong , Wu, Yue , Hu, Yating , Wang, Chengjie , Zhang, Qianqian , Liu, Jingbing et al. Advanced metal-organic framework-based membranes with ion selectivity for boosting electrochemical energy storage and conversion . | JOURNAL OF MATERIALS CHEMISTRY A , 2021 . |
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摘要 ：
Metal-organic framework (MOF) is a promising electrochromic material due to its high specific surface area and tunable pore size, which can benefit the fast transportation of ion/charge. Here, a simple solvothermal deposition method for fabrication of Ni-MOF 74 electrochromic films on ITO is developed. It is found that the reaction temperature has played an important role in the morphology and electrochromic performance of as-prepared Ni-MOF 74 film. The film prepared at the optimized temperature exhibits the best electrochromic performance with a rapid switching speed (the coloration/bleaching time = 24.5/23.5 s). In addition, the optimized film displays a high optical contrast of 44.4% at 550 nm and can be stably switched for 650 cycles with < 21.5% contrast attenuation. The electrochromism of Ni-MOF 74 can be attributed to the oxidized and reduced states of 2,5-dihydroxyterephthalic acid ligands. This simple method can be broaden to fabricate other metal-based MOF films for electrochromic applications.
关键词 ：
Electrochromic materials Electrochromic materials ITO substrate ITO substrate Ni-MOF 74 Ni-MOF 74 Thin film Thin film
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| GB/T 7714 | Zhang, Ning , Jin, Yuhong , Zhang, Qianqian et al. Direct fabrication of electrochromic Ni-MOF 74 film on ITO with high-stable performance [J]. | IONICS , 2021 , 27 (8) : 3655-3662 . |
| MLA | Zhang, Ning et al. "Direct fabrication of electrochromic Ni-MOF 74 film on ITO with high-stable performance" . | IONICS 27 . 8 (2021) : 3655-3662 . |
| APA | Zhang, Ning , Jin, Yuhong , Zhang, Qianqian , Liu, Jingbing , Zhang, Yongzhe , Wang, Hao . Direct fabrication of electrochromic Ni-MOF 74 film on ITO with high-stable performance . | IONICS , 2021 , 27 (8) , 3655-3662 . |
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摘要 ：
Metal organic frameworks (MOFs) have been considered as one of the most promising electrode materials for electrochemical capacitors due to their large specific surface area and abundant pore structure. Herein, we report a Co-MOF electrode with a vertical-standing 2D parallelogram-like nanoarray structure on a Ni foam substrate via a one-step solvothermal method. The as-prepared Co-MOF on a Ni foam electrode delivered a high area-specific capacitance of 582.0 mC cm(-2) at a current density of 2 mA cm(-2) and a good performance rate of 350.0 mC cm(-2) at 50 mA cm(-2). Moreover, an asymmetric electrochemical capacitor (AEC) device (Co-MOF on Ni foam//AC) was assembled by using the as-prepared Co-MOF on a Ni foam as the cathode and a active carbon-coated Ni foam as the anode to achieve a maximum energy density of 0.082 mW cm(-2) at a power density of 0.8 mW cm(-2), which still maintained 0.065 mW cm(-2) at a high power density of 11.94 mW cm(-2). Meanwhile, our assembled device exhibited an excellent cycling stability with a capacitance retention of nearly 100% after 1000 cycles. Therefore, this work provides a simple method to prepare MOF-based material for the application of energy storage and conversion.
关键词 ：
asymmetric electrochemical capacitors asymmetric electrochemical capacitors Co-MOF Co-MOF metal organic frameworks metal organic frameworks nanoarrays nanoarrays
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| GB/T 7714 | Li, Leyuan , Mi, Hongtian , Jin, Yuhong et al. Fabrication of Vertical-Standing Co-MOF Nanoarrays with 2D Parallelogram-like Morphology for Aqueous Asymmetric Electrochemical Capacitors [J]. | MOLECULES , 2021 , 26 (17) . |
| MLA | Li, Leyuan et al. "Fabrication of Vertical-Standing Co-MOF Nanoarrays with 2D Parallelogram-like Morphology for Aqueous Asymmetric Electrochemical Capacitors" . | MOLECULES 26 . 17 (2021) . |
| APA | Li, Leyuan , Mi, Hongtian , Jin, Yuhong , Ren, Dayong , Zhou, Kailing , Zhang, Qianqian et al. Fabrication of Vertical-Standing Co-MOF Nanoarrays with 2D Parallelogram-like Morphology for Aqueous Asymmetric Electrochemical Capacitors . | MOLECULES , 2021 , 26 (17) . |
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