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  • Wiley  (11)
  • Du, Wencheng  (11)
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  • Wiley  (11)
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  • 1
    In: Angewandte Chemie International Edition, Wiley
    Abstract: Gradual disability of Zn anode and high negative/positive electrode (N/P) ratio usually depreciate calendar life and energy density of aqueous Zn batteries (AZBs). Herein, within original Zn2+‐free hydrated electrolytes, a steric hindrance/electric field shielding‐driven “hydrophobic ion barrier” is engineered towards ultradurable (002) plane‐exposed Zn stripping/plating to solve this issue. Guided by theoretical simulations, hydrophobic adiponitrile (ADN) is employed as a steric hindrance agent to ally with inert electric field shielding additive (Mn2+) for plane adsorption priority manipulation, thereby constructing the “hydrophobic ion barrier”. This design robustly suppresses the (002) plane/dendrite growth, enabling ultradurable (002) plane‐exposed dendrite‐free Zn stripping/plating. Even being cycled in Zn‖Zn symmetric cell over 2150 h at 0.5 mA cm‐2, the efficacy remains well‐kept. Additionally, Zn‖Zn symmetric cells can be also stably cycled over 918 h at 1 mA cm‐2, verifying uncompromised Zn stripping/plating kinetics. As‐assembled anode‐less Zn‖VOPO4·2H2O full cells with a low N/P ratio (2:1) show a high energy density of 75.2 Wh kg‐1full electrode after 842 cycles at 1 A g‐1, far surpassing counterparts with thick Zn anode and low cathode loading mass, featuring excellent practicality. This study opens a new avenue by robust “hydrophobic ion barrier” design to develop long‐life anode‐less Zn batteries.
    Type of Medium: Online Resource
    ISSN: 1433-7851 , 1521-3773
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2024
    detail.hit.zdb_id: 2011836-3
    detail.hit.zdb_id: 123227-7
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  • 2
    In: Angewandte Chemie, Wiley
    Abstract: Gradual disability of Zn anode and high negative/positive electrode (N/P) ratio usually depreciate calendar life and energy density of aqueous Zn batteries (AZBs). Herein, within original Zn2+‐free hydrated electrolytes, a steric hindrance/electric field shielding‐driven “hydrophobic ion barrier” is engineered towards ultradurable (002) plane‐exposed Zn stripping/plating to solve this issue. Guided by theoretical simulations, hydrophobic adiponitrile (ADN) is employed as a steric hindrance agent to ally with inert electric field shielding additive (Mn2+) for plane adsorption priority manipulation, thereby constructing the “hydrophobic ion barrier”. This design robustly suppresses the (002) plane/dendrite growth, enabling ultradurable (002) plane‐exposed dendrite‐free Zn stripping/plating. Even being cycled in Zn‖Zn symmetric cell over 2150 h at 0.5 mA cm‐2, the efficacy remains well‐kept. Additionally, Zn‖Zn symmetric cells can be also stably cycled over 918 h at 1 mA cm‐2, verifying uncompromised Zn stripping/plating kinetics. As‐assembled anode‐less Zn‖VOPO4·2H2O full cells with a low N/P ratio (2:1) show a high energy density of 75.2 Wh kg‐1full electrode after 842 cycles at 1 A g‐1, far surpassing counterparts with thick Zn anode and low cathode loading mass, featuring excellent practicality. This study opens a new avenue by robust “hydrophobic ion barrier” design to develop long‐life anode‐less Zn batteries.
    Type of Medium: Online Resource
    ISSN: 0044-8249 , 1521-3757
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2024
    detail.hit.zdb_id: 506609-8
    detail.hit.zdb_id: 1479266-7
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  • 3
    In: Advanced Functional Materials, Wiley, Vol. 34, No. 17 ( 2024-04)
    Abstract: Aqueous Zn–metal batteries are considered promising candidates for next‐generation energy storage. However, low zinc utilization rate (ZUR) and limited cycle life are still hinder its commercial application because of severe parasitic side effects. Herein, inspired by the wound healing process, an innovative electrode recovery technology is developed to improve the comprehensive ZUR and prolong the cycling life through repetitive rejuvenation of zinc anode by designing chitosan‐based homologous gel/solid synergistic electrolyte. The designed synergistic electrolyte, consisting of protonated chitosan gel electrolyte and Zn‐chitosan solid electrolyte, exhibits superior zinc ion diffusion capability and low free‐water activity, leading to dendrite‐free Zn deposition and HER inhibition. Moreover, through proton neutralization and zinc ion complexation, the formulated electrolyte can implement the rejuvenation of zinc anode by smoothing interfacial defects and eliminating parasitic byproducts. Consequently, the gel/solid synergistic electrolyte displays reversible Zn plating/stripping chemistry for 4000 cycles with high average Coulombic efficiency (99.8%) and realizes comprehensive ZUR of 97.4% through four iterations of electrode recover under extreme conditions (20 mA cm −2 , 31.5% Zn depth of discharge), noticeably higher than zinc electrode with no recover (11.8%). Furthermore, the superiority of customized synergistic electrolyte is further demonstrated by coupling with I 2 cathode and achieving impressive 36 000 stable cycles.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2024
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
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  • 4
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Advanced Functional Materials Vol. 31, No. 4 ( 2021-01)
    In: Advanced Functional Materials, Wiley, Vol. 31, No. 4 ( 2021-01)
    Abstract: With the constant focus on energy storage devices, layered materials are ideal electrodes for the new generation of highly efficient secondary ion batteries and supercapacitors due to their flexible 2D structures and high theoretical capacities. However, the small interlayer distances in layered electrode materials and the strong Columbic interactions between the working ions and host lattice anions cause slow ion diffusion. In addition, structural collapse during repeated ion insertion and extraction reduces the cycling lifetime. As such, interlayer engineering strategies are effective approaches to optimize ion transmission kinetics and structural integrity. In view of the latest research on the interlayer engineering of layered materials, this review will discuss useful strategies to improve electrode performance. The synthetic strategies, characterization techniques, and effects of interlayer‐engineered layered materials, including metal oxides, metal sulfides, carbonous materials, and MXenes, are discussed in detail. The future outlook and challenges for interlayer engineering are also presented, which may pave the way for the development of new layered materials.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
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  • 5
    In: Advanced Functional Materials, Wiley, Vol. 31, No. 3 ( 2021-01)
    Abstract: Environment‐friendly and low‐cost aqueous zinc‐ion batteries (ZIBs) have received considerable attention for large‐scale energy storage. However, the low coulombic efficiency and potential safety hazards of Zn‐metal anodes severely hinder their practical implementations. Herein, for the first time, mixed‐valence Cu 2− x Se is proposed as a new intercalation anode to construct Zn‐metal‐free rocking‐chair ZIBs with a long lifespan. It is found that the introduction of low‐valence Cu not only modify active sites for Zn 2+ ion storage, but also optimizes the electronic interaction between the active sites and the intercalated Zn 2+ ion, leading to a favorable intercalation formation energy (−0.68 eV) and reduced diffusion barrier, as demonstrated by first‐principles calculation. Ex situ X‐ray diffraction, ex situ transmission electron microscopy and galvanostatic intermittent titration technique measurements reveal the reversible insertion/extraction of Zn 2+ in Cu 2− x Se via an intercalation reaction mechanism. Owing to the rigid host structure and facile Zn 2+ diffusion kinetics, the Cu 2− x Se nanorod anode shows an enhanced coulombic efficiency (above 99.5%), outstanding rate capability and excellent cycling stability. The as‐fabricated Zn x MnO 2 ||Cu 2− x Se Zn‐ion full battery exhibits an impressive electrochemical performance, particularly an ultralong cycle life of over 20 000 cycles at 2 A g −1 . This study is expected to provide new opportunities for developing high‐performance rechargeable aqueous ZIBs.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
    Location Call Number Limitation Availability
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2021
    In:  Advanced Functional Materials Vol. 31, No. 22 ( 2021-05)
    In: Advanced Functional Materials, Wiley, Vol. 31, No. 22 ( 2021-05)
    Abstract: Rechargeable zinc‐ion batteries (ZIBs) have recently attracted attention for applications in energy storage systems owing to their intrinsic safety, low cost, environmental compatibility, and competitive gravimetric energy density. To enable the practical applications of ZIBs, their energy density must be equivalent to the existing commercial lithium‐ion batteries. To acquire high‐energy density, increasing the operating voltage of the battery is undoubtedly an effective method, which demands cathode material to exhibit a high voltage versus Zn 2+ /Zn, while matching a highly reversible anode and an electrolyte with a sufficiently wide electrochemical stability window. This review focuses on the design strategies and challenges towards high‐voltage ZIBs. First, the basic electrochemistry of ZIBs and the recent progress in various high‐voltage cathode materials for ZIBs, including Prussian blue analogs, polyanionic compounds, and metal‐based oxides are introduced. The challenges and corresponding countermeasures of these materials are discussed, while strategies to further improve the cathode operating voltage, influence factors of voltage in the redox reaction, and energy storage mechanism are also illustrated. The following section describes the strategies towards high‐performance Zn anode, and summarizes the electrolytes that can help increase the battery voltage. The final section outlines the potential development in ZIBs.
    Type of Medium: Online Resource
    ISSN: 1616-301X , 1616-3028
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2029061-5
    detail.hit.zdb_id: 2039420-2
    SSG: 11
    Location Call Number Limitation Availability
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  • 7
    In: Angewandte Chemie International Edition, Wiley, Vol. 63, No. 15 ( 2024-04-08)
    Abstract: Bipolar organic cathode materials (OCMs) implementing cation/anion storage mechanisms are promising for high‐energy aqueous Zn batteries (AZBs). However, conventional organic functional group active sites in OCMs usually fail to sufficiently unlock the high‐voltage/capacity merits. Herein, we initially report dynamically ion‐coordinated bipolar OCMs as cathodes with chalcogen active sites to solve this issue. Unlike conventional organic functional groups, chalcogens bonded with conjugated group undergo multielectron‐involved positive‐valence oxidation and negative‐valence reduction, affording higher redox potentials and reversible capacities. With phenyl diselenide (PhSe‐SePh, PDSe) as a proof of concept, it exhibits a conversion pathway from (PhSe) − to (PhSe‐SePh) 0 and then to (PhSe) + as unveiled by characterization and theoretical simulation, where the diselenide bonds are periodically broken and healed, dynamically coordinating with ions (Zn 2+ and OTF − ). When confined into ordered mesoporous carbon (CMK‐3), the dissolution of PDSe intermediates is greatly inhibited to obtain an ultralong lifespan without voltage/capacity compromise. The PDSe/CMK‐3 || Zn batteries display high reversibility capacity (621.4 mAh g PDSe −1 ), distinct discharge plateau (up to 1.4 V), high energy density (578.3 Wh kg PDSe −1 ), and ultralong lifespan (12 000 cycles) at 10 A g −1 , far outperforming conventional bipolar OCMs. This work sheds new light on conversion‐type active site engineering for high‐voltage/capacity bipolar OCMs towards high‐energy AZBs.
    Type of Medium: Online Resource
    ISSN: 1433-7851 , 1521-3773
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2024
    detail.hit.zdb_id: 2011836-3
    detail.hit.zdb_id: 123227-7
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  • 8
    In: Chemistry – A European Journal, Wiley, Vol. 26, No. 29 ( 2020-05-20), p. 6554-6560
    Abstract: Lithium ion batteries (LIBs) at present still suffer from low rate capability and poor cycle life during fast ion insertion/extraction processes. Searching for high‐capacity and stable anode materials is still an ongoing challenge. Herein, a facile strategy for the synthesis of ultrathin GeS 2 nanosheets with the thickness of 1.1 nm is reported. When used as anodes for LIBs, the two‐dimensional (2D) structure can effectively increase the electrode/electrolyte interface area, facilitate the ion transport, and buffer the volume expansion. Benefiting from these merits, the as‐synthesized GeS 2 nanosheets deliver high specific capacity (1335 mAh g −1 at 0.15 A g −1 ), extraordinary rate performance (337 mAh g −1 at 15 A g −1 ) and stable cycling performance (974 mAh g −1 after 200 cycles at 0.5 A g −1 ). Importantly, our fabricated Li‐ion full cells manifest an impressive specific capacity of 577 mAh g −1 after 50 cycles at 0.1 A g −1 and a high energy density of 361 Wh kg −1 at a power density of 346 W kg −1 . Furthermore, the electrochemical reaction mechanism is investigated by the means of ex‐situ high‐resolution transmission electron microscopy. These results suggest that GeS 2 can use to be an alternative anode material and encourage more efforts to develop other high‐performance LIBs anodes.
    Type of Medium: Online Resource
    ISSN: 0947-6539 , 1521-3765
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 1478547-X
    detail.hit.zdb_id: 1231884-X
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  • 9
    In: Angewandte Chemie, Wiley, Vol. 136, No. 15 ( 2024-04-08)
    Abstract: Bipolar organic cathode materials (OCMs) implementing cation/anion storage mechanisms are promising for high‐energy aqueous Zn batteries (AZBs). However, conventional organic functional group active sites in OCMs usually fail to sufficiently unlock the high‐voltage/capacity merits. Herein, we initially report dynamically ion‐coordinated bipolar OCMs as cathodes with chalcogen active sites to solve this issue. Unlike conventional organic functional groups, chalcogens bonded with conjugated group undergo multielectron‐involved positive‐valence oxidation and negative‐valence reduction, affording higher redox potentials and reversible capacities. With phenyl diselenide (PhSe‐SePh, PDSe) as a proof of concept, it exhibits a conversion pathway from (PhSe) − to (PhSe‐SePh) 0 and then to (PhSe) + as unveiled by characterization and theoretical simulation, where the diselenide bonds are periodically broken and healed, dynamically coordinating with ions (Zn 2+ and OTF − ). When confined into ordered mesoporous carbon (CMK‐3), the dissolution of PDSe intermediates is greatly inhibited to obtain an ultralong lifespan without voltage/capacity compromise. The PDSe/CMK‐3 || Zn batteries display high reversibility capacity (621.4 mAh g PDSe −1 ), distinct discharge plateau (up to 1.4 V), high energy density (578.3 Wh kg PDSe −1 ), and ultralong lifespan (12 000 cycles) at 10 A g −1 , far outperforming conventional bipolar OCMs. This work sheds new light on conversion‐type active site engineering for high‐voltage/capacity bipolar OCMs towards high‐energy AZBs.
    Type of Medium: Online Resource
    ISSN: 0044-8249 , 1521-3757
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2024
    detail.hit.zdb_id: 506609-8
    detail.hit.zdb_id: 1479266-7
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  • 10
    In: Advanced Energy Materials, Wiley, Vol. 13, No. 38 ( 2023-10)
    Abstract: Zn powder is considered as a potential Zn metal anode for aqueous Zn‐ion batteries. However, restricted ion/electron transfer and volume effect‐caused electrical contact failure in conventional polymer binder composited Zn powder anodes deteriorate their electrochemical performance. Here, a high‐performance soft solid‐like viscoelastic Zn powder composite anode is proposed based on an oligomer gluing strategy. Benefiting from the viscoelastic properties, the soft‐solid Zn powder composite (ss‐ZnP) anode has significantly enhanced charge transfer, alleviated volume effect, and homogenized interfacial electric field, leading to fast plating/stripping kinetics and dendrite‐free deposition morphology. Furthermore, the assembled NH 4 V 4 O 10 ‖ss‐ZnP full cell delivers higher capacity (510 mAh g −1 at 0.1A g −1 , 300 mAh g −1 at 1A g −1 ) and longer lifespan up to 500 cycles at 1 A g −1 , superior to conventional polymer binder composited Zn powder anode and other reported rheological Zn powder‐based anodes. Apart from the electrochemical merits, this soft matter‐based design also endows the ss‐ZnP electrode with free‐standing and malleable properties which greatly expand its practical application.
    Type of Medium: Online Resource
    ISSN: 1614-6832 , 1614-6840
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2555492-X
    detail.hit.zdb_id: 2594556-7
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