Publications by authors named "Shi Xue Dou"

The utilization of cobalt-based sulfides is constrained by their inherently low conductivity and slow sodium ion diffusion kinetics. Modifying the electronic configuration and constructing heterostructures are promising strategies to enhance intrinsic conductivity and expedite the sodium ion diffusion process. In this study, heterogeneous nanoparticles of Se-substituted CoS/CoSe, embedded within heteroatom-modified carbon nanosheet, were synthesized using metal molten salt-assisted dimensionality reduction alongside concurrent sulfurization and selenization techniques.

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Aqueous zinc ion batteries (AZIBs) are experiencing rapid development due to their high theoretical capacity, abundant zinc resources, and intrinsic safety. However, the progress of AZIBs is hindered by uncontrollable parasitic reactions and excessive dendrite growth, which compromise the durability and effective utilization of zinc metal anodes. To address these challenges, the study has constructed a 3D crosslinked macromolecular network composed of zinc ion-bonded potato starch (StZ) as an interface layer on Zn foil (StZ-Zn) to inhibit hydrogen evolution, regulate Zn flux, and ensure uniform Zn deposition.

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Severe structural evolution and high content of [Fe(CN)] defects drastically deteriorate K-ion storage performances of Prussian blue-based cathodes. Herein, a potassium manganese iron copper hexacyanoferrate (KFeMnCuHCF), with suppressed anionic vacancies, eliminated band gap, and low K-ion diffusion barrier, is regarded as a cathode for potassium-ion batteries. The entropy stabilization effect and robust Cu-N bond induced by the inert Cu-ion with large electronegativity boost KFeMnCuHCF to exhibit great phase state stability, thus inhibiting the structural transition of monoclinic ↔ cubic.

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The environmental problems caused by the abuse of antibiotics are raising serious attention, and the removal of antibiotics in wastewater is meaningful yet challenging. In this work, lignin-derived carbon fibers loaded layered double hydroxides (LDH@LCF) has been prepared for the removal of ofloxacin (OFX) from wastewater via photocatalysis, which exhibit a high degradation efficiency of 96 % under visible light and maintained 90 % after five reuses. The effects of Zn/Fe in the samples and other parameters affecting the photocatalytic efficiency of OFX have been systematically investigated.

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Rechargeable batteries have been indispensable for various portable devices, electric vehicles, and energy storage stations. The operation of rechargeable batteries at low temperatures has been challenging due to increasing electrolyte viscosity and rising electrode resistance, which lead to sluggish ion transfer and large voltage hysteresis. Advanced electrolyte design and feasible electrode engineering to achieve desirable performance at low temperatures are crucial for the practical application of rechargeable batteries.

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Rechargeable aqueous Zn metal batteries (AZMBs) are attractive for stationary energy storage due to their low cost and high safety. However, their practical application is hindered by the excessive use of zinc anodes and poor high-temperature performance, caused by severe side reactions and dendritic growth issues. Here, an electrolyte design strategy is reported based on bidentate coordination of Zn and solvent to tailor the solvation structure.

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Transition metal phosphides (TMPs) show promise in water electrolysis due to their electronic structures, which activate hydrogen/oxygen reaction intermediates. However, TMPs face limitations in catalytic efficiency due to insufficient active sites, poor conductivity, and multiple intermediate steps in water electrolysis. Here, we synthesize a highly efficient bifunctional self-supported electrocatalyst, which consists of an N-doped carbon shell anchored on Fe-doped CoP/CoP arrays on nickel foam (NC@Fe-CoP/NF) using hydrothermal and phosphorization techniques.

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Solid polymer electrolytes (SPEs) represent a pivotal advance toward high-energy solid-state lithium metal batteries. However, inadequate interfacial contact remains a significant bottleneck, impeding scalability and application. Inadequate interfacial contact remains a significant bottleneck, impeding scalability and application.

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O3-type layered oxides have been extensively studied as cathode materials for sodium-ion batteries due to their high reversible capacity and high initial sodium content, but they suffer from complex phase transitions and an unstable structure during sodium intercalation/deintercalation. Herein, we synthesize a high-entropy O3-type layered transition metal oxide, NaNiCuFeMnMgTiO (NCFMMT), by simultaneously doping Cu, Mg, and Ti into its transition metal layers, which greatly increase structural entropy, thereby reducing formation energy and enhancing structural stability. The high-entropy NCFMMT cathode exhibits significantly improved cycling stability (capacity retention of 81.

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The development of cost-efficient, long-lifespan, and all-climate sodium-ion batteries is of great importance for advancing large-scale energy storage but is plagued by the lack of suitable cathode materials. Here, we report low-cost Na-rich Mn-based Prussian blue analogues with superior rate capability and ultralong cycling stability over 10,000 cycles via structural optimization with electrochemically inert Ni atoms. Their thermal stability, all-climate properties, and potential in full cells are investigated in detail.

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Lithium metal batteries (LMBs), with high energy densities, are strong contenders for the next generation of energy storage systems. Nevertheless, the unregulated growth of lithium dendrites and the unstable solid electrolyte interphase (SEI) significantly hamper their cycling efficiency and raise serious safety concerns, rendering LMBs unfeasible for real-world implementation. Covalent organic frameworks (COFs) and their derivatives have emerged as multifunctional materials with significant potential for addressing the inherent problems of the anode electrode of the lithium metal.

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Developing low-cost and highly efficient bifunctional catalysts for both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER) is a challenging problem in electrochemical overall water splitting. Here, iron, tungsten dual-doped nickel sulfide catalyst (Fe/W-NiS) is synthesized on the nickel foam, and it exhibits excellent OER and HER performance. As a result, the water electrolyze based on Fe/W-NiS bifunctional catalyst illustrates 10 mA cm at 1.

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Article Synopsis
  • Scientists are studying P3-layered transition oxide cathodes because they can hold a lot of energy and work quickly for sodium-ion batteries.
  • However, they have a problem where their performance decreases over time due to changes in their structure and the movement of manganese particles.
  • To fix this, researchers created a special material that combines P3 with another structure (spinel), which helps the batteries last longer and perform better.
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Regulating the electric double layer (EDL) structure of the zinc metal anode by using electrolyte additives is an efficient way to suppress interface side reactions and facilitate uniform zinc deposition. Nevertheless, there are no reports investigating the proactive design of EDL-regulating additives before the start of experiments. Herein, a functional group assembly strategy is proposed to design electrolyte additives for modulating the EDL, thereby realizing a long-lasting zinc metal anode.

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Sodium ion batteries (SIBs) are considered as the ideal candidates for the next generation of electrochemical energy storage devices. The major challenges of anode lie in poor cycling stability and the sluggish kinetics attributed to the inherent large Na size. In this work, Bi nanosphere encapsulated in N-doped carbon nanowires (Bi@N-C) is assembled by facile electrospinning and carbonization.

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The effective flow of electrons through bulk electrodes is crucial for achieving high-performance batteries, although the poor conductivity of homocyclic sulfur molecules results in high barriers against the passage of electrons through electrode structures. This phenomenon causes incomplete reactions and the formation of metastable products. To enhance the performance of the electrode, it is important to place substitutable electrification units to accelerate the cleavage of sulfur molecules and increase the selectivity of stable products during charging and discharging.

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In this work, 2D ferromagnetic MGeTe (MGT, M = Ni/Fe) nanosheets with rich atomic Te vacancies (2D-MGT) are demonstrated as efficient OER electrocatalyst via a general mechanical exfoliation strategy. X-ray absorption spectra (XAS) and scanning transmission electron microscope (STEM) results validate the dominant presence of metal-O moieties and rich Te vacancies, respectively. The formed Te vacancies are active for the adsorption of OH* and O* species while the metal-O moieties promote the O* and OOH* adsorption, contributing synergistically to the faster oxygen evolution kinetics.

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Sodium-ion batteries (SIBs) are experiencing a large-scale renaissance to supplement or replace expensive lithium-ion batteries (LIBs) and low energy density lead-acid batteries in electrical energy storage systems and other applications. In this case, layered oxide materials have become one of the most popular cathode candidates for SIBs because of their low cost and comparatively facile synthesis method. However, the intrinsic shortcomings of layered oxide cathodes, which severely limit their commercialization process, urgently need to be addressed.

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Article Synopsis
  • Room-temperature sodium-sulfur (RT-Na/S) batteries are seen as high-potential energy storage solutions, but their practical use is hindered by issues related to their performance under real-world conditions.
  • The review discusses recent advancements in key components of RT-Na/S batteries, including the sodium metal anode, sulfur cathode, electrolyte, and separators, focusing on how these elements perform in practical scenarios with specific parameters like high sulfur loading and lean electrolytes.
  • An empirical equation is introduced for estimating the energy density of RT-Na/S pouch cells in practical conditions, highlighting the importance of aligning lab findings with real-world applications to enhance the usability of these batteries.
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Prussian blue analogues (PBAs) have been widely studied as cathodes for potassium-ion batteries (PIBs) due to their three-dimensional framework structure and easily adjustable composition. However, the phase transition behavior and [Fe(CN)] anionic defects severely deteriorate electrochemical performances. Herein, we propose a defect-free potassium iron manganese hexacyanoferrate (KFeMn[Fe(CN)]·1.

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Rechargeable aqueous zinc ion batteries (AZIBs) have gained considerable attention owing to their low cost and high safety, but dendrite growth, low plating/stripping efficiency, surface passivation, and self-erosion of the Zn metal anode are hindering their application. Herein, a one-step molecular engineering strategy for the simultaneous construction of hierarchical MoS double-layer nanotubes (MoS-DLTs) with expanded layer-spacing, oxygen doping, structural defects, and an abundant 1T-phase is proposed, which are designed as an intercalation-type anode for "rocking-chair" AZIBs, avoiding the Zn anode issues and therefore displaying a long cycling life. Benefiting from the structural optimization and molecular engineering, the Zn diffusion efficiency and interface reaction kinetics of MoS-DLTs are enhanced.

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Linearly interlinked single atoms offer unprecedented physiochemical properties, but their synthesis for practical applications still poses significant challenges. Herein, linearly interlinked iron single-atom catalysts that are loaded onto interconnected carbon channels as cathodic sulfur hosts for room-temperature sodium-sulfur batteries are presented. The interlinked iron single-atom exhibits unique metallic iron bonds that facilitate the transfer of electrons to the sulfur cathode, thereby accelerating the reaction kinetics.

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Enhancing the mobility of lithium-ions (Li) through surface engineering is one of major challenges facing fast-charging lithium-ion batteries (LIBs). In case of demanding charging conditions, the use of a conventional artificial graphite (AG) anode leads to an increase in operating temperature and the formation of lithium dendrites on the anode surface. In this study, a biphasic zeolitic imidazolate framework (ZIF)-AG anode, designed strategically and coated with a mesoporous material, is verified to improve the pathways of Li and electrons under a high charging current density.

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Exploring economical, efficient, and stable electrocatalysts for the seawater hydrogen evolution reaction (HER) is highly desirable but is challenging. In this study, a Mo cation doped NiSe/MoSe heterostructural electrocatalyst, Mo-NiSe/MoSe, was successfully prepared by simultaneously doping Mo cations into the NiSe lattice (Mo-NiSe) and growing atomic MoSe nanosheets epitaxially at the edge of the Mo-NiSe. Such an Mo-NiSe/MoSe catalyst requires only 110 mV to drive current densities of 10 mA cm in alkaline simulated seawater, and shows almost no obvious degradation after 80 h at 20 mA cm.

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