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Rare Metals 2024年第4期43卷 1580-1588页

作者： Shabana Shaheen Shuai Xu Ji Bian Amir Zada Zi-Qing Zhang Yang Qu Li-Qiang Jing Key laboratory of Functional Inorganic materials chemistry (Ministry of Education) International Joint Research Center and Lab for Catalytic TechnologySchool of Chemistry and Materials ScienceHeilongjiang University Department of chemistry Abdul Wali Khan University

It is highly desired to develop efficient photocatalysts with recycling property for practical application to degrade toxic pollutants.Herein,nanosheet-assembled NiFe2O4microspheres with commendable activity are successfully synthesized by a facile solvothermal reaction with NH4F as the modifier,and their photoactivities are further improved by coupling with NiO through an in situ growth process.The optimized nickel oxide（NiO）/nickel ferrite（NiFe2O4） microsphere composite（5NiO/NFO-4）exhibits a satisfactory photocatalytic activity for 2,4-dichlorophenol（2,4-DCP） degradation under visible-light irradiation,which is attributed to its wide visible-light response,well-designed hierarchical structure and enhanced charge transfer and separation by coupling NiO as a high-level energy platform to accept electrons.Moreover,it is found that the NiO/NiFe2O4microsphere photocatalysts can be easily collected and recycled owing to the distinctive magnetic properties.This work provides a feasible route to rational design visible-light-driven photocatalysts with high-activity for environmental remediation and purification with good recyclability.

关键词： NiFe 2 O 4 microspheres NiO/NiFe 2 O 4 composite Charge separation Visible-light photocatalysis 2,4-Dichlorophenol degradation

Coupling Sb_(2)WO_(6)microflowers and conductive polypyrrole for efficient potassium storage by enhanced conductivity and K^(+) diffusivity

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Journal of Energy chemistry 2024年第2期89卷 250-258,I0007页

作者： Ruiqi Tian Hehe Zhang Zeyu Yuan Yuehua Man Jianlu Sun Jianchun Bao Ming-Sheng Wang Xiaosi Zhou School of chemistry and materials Science Nanjing Normal UniversityNanjing 210023JiangsuChina State Key lab of Physical chemistry of Solid Surfaces College of MaterialsXiamen UniversityXiamen 361005FujianChina

Although metal oxide compounds are considered as desirable anode materials for potassium-ion batteries(PIBs)due to their high theoretical capacity,the large volume variation remains a key issue in realizing metal oxide anodes with long cycle life and excellent rate property.In this study,polypyrroleencapsulated Sb_(2)WO_(6)(denoted Sb_(2)WO_(6)@PPy)microflowers are synthesized by a one-step hydrothermal method followed by in-situ polymerization and coating by pyrrole.Leveraging the nanosheet-stacked Sb_(2)WO_(6)microflower structure,the improved electronic conductivity,and the architectural protection offered by the PPy coating,Sb_(2)WO_(6)@PPy exhibits boosted potassium storage properties,thereby demonstrating an outstanding rate property of 110.3 m A h g^(-1)at 5 A g^(-1)and delivering a long-period cycling stability with a reversible capacity of 197.2 m A h g^(-1)after 500 cycles at 1 A g^(-1).In addition,the conversion and alloying processes of Sb_(2)WO_(6)@PPy in PIBs with the generation of intermediates,K_(2)WO_(4)and K_(3)Sb,is determined by X-ray photoelectron spectroscopy,transmission electron microscopy,and exsitu X-ray diffraction during potassiation/depotassiation.Density functional theory calculations demonstrate that the robust coupling between PPy and Sb_(2)WO_(6)endues it with a much stronger total density of states and a built-in electric field,thereby increasing the electronic conductivity,and thus effectively reduces the K^(+)diffusion barrier.

关键词： Sb_(2)WO_(6) Polypyrrole coating Anode Potassium-ion battery In-situ TEM observation

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Construction of electron rich Fe active sites by FeCu alloy anchoring on carbon nitride for photocatalytic nitrogen reduction

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Rare Metals 2024年第4期43卷 1570-1579页

作者： Gang Dong Cong Huang Fei-Yang Chen Xue-Qin Liu Zhen Li Xiao-Li Su Tao Zeng Yun-Xia Chen Yi-Huang Chen Yang Wang School of materials Science and Engineering Jingdezhen Ceramic University Faculty of materials Science and chemistry China University of Geosciences College of chemistry and materials Engineering Wenzhou University

Given the clean and inexhaustible solar energy from solar light,photocatalytic ammonia synthesis is extremely appealing.However,high electron-hole recombination rates and insufficient active sites severely limited N2 photoreaction reduction.Herein,we designed and fabricated FeCu alloy nanoparticles anchored on carbon nitride nanosheets with excellent photocatalyt ic ammonia synthesis performance.As a coupler between Fe and carbon nitride,Cu promotes the separation of photogenerated charge carriers in carbon nitride under solar light irradiation,and renters the semiconductor a forceful electron donor for the Fe active sites.The accumulated electrons at Fe sites furtherly facilitated the adsorption and activation of the molecular nitrogen.Besides,the uniform dispersed FeCu alloy nanoparticles were on carbon nitride nanosheets enhanced the stability of photocataly tic nitrogen reduction reaction,making the artificial photocataly tic ammonia synthesis more sustainable for application.This work highlights that a direct electron transfer channel can be used to regulate the photochemical nitrogen fixation network.

关键词： Photocatalytic N 2 fixation Carbon nitride FeCu alloy Active sites Hydrogenation pathway

Micelle-directed self-assembly of single-crystal-like mesoporous stoichiometric oxides for high-performance lithium storage

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National Science Review 2024年第4期11卷 195-205页

作者： Yanhua Wan Changyao Wang Xingmiao Zhang Yang Yin Mengmeng Liu Bing Ma Linlin Duan Yuzhu Ma Wei Zhang Changlin Zheng Dongliang Chao Fei Wang Yongyao Xia Wei Li Department of chemistry Laboratory of Advanced Materials Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials State Key Laboratory of Molecular Engineering of Polymers College of Chemistry and Materials ScienceFudan University State Key laboratory of Surface Physics and Department of Physics Fudan University

Due to their uncontrollable assembly and crystallization process,the synthesis of mesoporous metal oxide single crystals remains a formidable challenge.Herein,we report the synthesis of single-crystal-like mesoporous Li2TiSiO5by using soft micelles as templates.The key lies in the atomic-scale self-assembly and step-crystallization processes,which ensure the formation of single-crystal-like mesoporous Li2TiSiO5microparticles via an oriented attachment growth mechanism under the confinement of an in-situ formed carbon matrix.The mesoporous Li2TiSiO5anode achieves a superior rate capability(148 mAh g-1at5.0 A g-1) and outstanding long-term cycling stability(138 mAh g-1after 3000 cycles at 2.0 A g-1) for lithium storage as a result of the ultrafast Li+diffusion caused by penetrating mesochannels and nanosized crystal frameworks（5-10 nm）.In comparison,bulk Li2TiSiO5exhibits poor rate capability and cycle performance due to micron-scale diffusion lengths.This method is very simple and reproducible,heralding a new way of designing and synthesizing mesoporous single crystals with controllable frameworks and chemical functionalities.

关键词： mesoporous materials micelles single-crystal-like Li2TiSiO5 lithium-ion batteries

Construction of plum-branch-like CoSe2@N-Doped carbon/carbon fiber with dual protective mechanisms for enhanced lithium storage

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Progress in Natural Science:materials International 2024年第3期34卷 495-502页

作者： Ying Wang Ming Zhang Lei Chen Yanjuan Li Qingqing Wang Xiaobin Wu Lingdi Shen Xiao Yan School of chemistry & materials Science Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials Jiangsu Normal University

Cobalt selenide（CoSe2） emerges as a highly promising anode material for lithium-ion batteries（LIBs） owing to its high theoretical capacity and cost-effectiveness. Despite these merits, its practical utilization faces challenges stemming from substantial volume fluctuations and limited electronic conductivity. To tackle these issues, a plumbranch-like structure of CoSe2@N-doped carbon that embedded in one-dimensional N-doped carbon fibers（CoSe2@NC/CFs）, is successfully synthesized through an in-situ confinement method. Well-defined CoSe2@NC nanoparticles, featuring diameters between 20～30 nm, are uniformly dispersed on both the inner and outer surfaces of the carbon fibers. The distinctive architecture of CoSe2@NC/CFs ensures an increased number of active sites, elevated electronic conductivity, alleviated volume expansion, and accelerated reaction kinetics.Consequently, the CoSe2@NC/CFs exhibits remarkable cycling performance and exceptional rate capability.Operating at a current density of 1000 mA g-1, the CoSe2@NC/CFs anode sustains a capacity of 664 mA h g-1with no obvious capacity decay over 500 cycles. Even at a high current density of 5000 mA g-1, it maintains a capacity of 445 mA h g-1with a mere 0.02 % capacity decay per cycle. This study introduces a novel approach to anode material design, showcasing significant advancements in lithium-ion battery technology.

关键词： Carbon fiber Electrochemical performances Electrode Lithium-ion battery Metal-selenide

The Current Progress and Challenges of Carbonized Polymer Dot-Based Room-Temperature Phosphorescent materials

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CCS chemistry 2024年第3期6卷 604-622页

作者： Chengyu Zheng Songyuan Tao Bai Yang State Key lab of Supramolecular Structure and materials College of ChemistryJilin UniversityChangchun 130012

Carbonized polymer dots(CPDs)as one type of carbon dots have attracted widespread attention in recent years.The proposal of the“shell–core”structure of CPDs leads to further thinking about the association between their special structures and luminescent properties.In recent years,great progress has been made in the field of CPD-based room-temperature phosphorescent materials.This review pays particular attention to how the special“core–shell”structure of CPDs influences the activation of roomtemperature phosphorescence(RTP).The strategies and vital factors to activate RTP for CPD-based materials in both solid state and water were reviewed in detail to elaborate on the effect of the special structure on RTP generation.Furthermore,some perspectives on the current challenges were also provided to guide the further development of CPD-based room-temperature phosphorescent materials.

关键词： room-temperature phosphorescent materials carbon dots carbonized polymer dots “core-shell”structure photoluminescent mechanism

Rational modulation of electronic structure in PtAuCuNi alloys boosts efficient electrocatalytic ethanol oxidation assisted with energy-saving hydrogen evolution

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Journal of Energy chemistry 2024年第6期93卷 557-567,I0014页

作者： Hu Yao Yinan Zheng Xin Yu Songjie Hu Baolian Su Xiaohui Guo Key lab of Synthetic and Natural Functional Molecule chemistry of Ministry of Education The College of Chemistry and Materials ScienceNorthwest UniversityXi’an 710069ShaanxiChina Department of Inorganic chemistry University of NamurBruxellesB-5000 NamurBelgium

Compared to conventional electrocatalytic water splitting,electrocatalytic ethanol oxidation reaction(EOR)along with hydrogen production is considered a more energy-efficient strategy.Herein,we prepared a type of novel quaternary alloy catalyst(PtAuCuNi@NF)that exhibits excellent activity for EOR(0.215 V at 10 mA cm^(-2))and hydrogen evolution reaction(HER)(7 mV at 10 mA cm^(-2)).Experimental results demonstrated that both Cu and Ni modulated the electronic environment around Pt and Au.The electron-rich active center facilitates the rapid adsorption and dissociation of reactants and intermediates for both EOR and HER.Impressively,in the ethanol-assisted overall water splitting(E-OWS),a current density of 10 mA cm^(-2)was achieved at 0.28 V.Moreover,an advanced acid-base self-powered system(A-Bsps)that can achieve a self-powered voltage of 0.59 V was assembled.Accordingly,the self-driven hydrogen production with zero external power supply was realized by integrating A-Bsps with the E-OWS equipment.The interesting results can provide a feasible strategy for designing and developing advanced nanoalloy-based materials for clean energy integration and use in various fields.

关键词： Pt-based alloy Electronic structure Ethanol oxidation Self-powered system Overall water splitting

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High-speed flexible near-infrared organic photodiode for optical communication

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National Science Review 2024年第3期11卷 227-238页

作者： Yu Zhu Hongbin Chen Ruiman Han Hao Qin Zhaoyang Yao Hang Liu Yanfeng Ma Xiangjian Wan Guanghui Li Yongsheng Chen The Centre of Nanoscale Science and Technology and Key laboratory of Functional Polymer materials Institute of Polymer ChemistryTianjin Key Laboratory of Functional Polymer Materials College of Chemistry and Renewable Energy Conversion and Storage Center(RECAST) Nankai University State Key laboratory of Elemento-Organic chemistry Nankai University

Optical communication is a particularly compelling technology for tackling the speed and capacity bottlenecks in data communication in modern society. Currently, the silicon photodetector plays a dominant role in high-speed optical communication across the visible-near-infrared spectrum. However, its intrinsic rigid structure, high working bias and low responsivity essentially limit its application in next-generation flexible optoelectronic devices. Herein, we report a narrow-bandgap non-fullerene acceptor（NFA） with a remarkable π-extension in the direction of both central and end units（CH17） with respect to the Y6 series, which demonstrates a more effective and compact 3D molecular packing, leading to lower trap states and energetic disorders in the photoactive film. Consequently, the optimized solution-processed organic photodetector（OPD） with CH17 exhibits a remarkable response time of 91 ns（λ = 880 nm） due to the high charge mobility and low parasitic capacitance, exceeding the values of most commercial Si photodiodes and all NFA-based OPDs operating in self-powered mode. More significantly, the flexible OPD exhibits negligible performance attenuation（<1%） after bending for 500 cycles, and maintains 96% of its initial performance even after 550 h of indoor exposure. Furthermore, the high-speed OPD demonstrates a high data transmission rate of 80 MHz with a bit error rate of 3.5 × 10-4, meaning it has great potential in next-generation high-speed flexible optical communication systems.

关键词： flexible organic photodetector high-speed NIR organic photodetector optical communication light fidelity narrow-bandgap non-fullerene acceptors

Intrinsic pentagon defect engineering in multiple spatial-scale carbon frameworks for efficient triiodide reduction

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Journal of Energy chemistry 2024年第8期95卷 20-28页

作者： Siyi Hou Xuedan Song Chang Yu Jiangwei Chang Yiwang Ding Yingbin Liu Xiubo Zhang Weizhe Liu Jieshan Qiu State Key lab of Fine Chemicals Liaoning Key Lab for Energy Materials and Chemical Engineering Frontier Science Center for Smart Materials School of Chemical EngineeringDalian University of Technology Liaoning Key lab for Energy materials and Chemical Engineering Frontier Science Center for Smart Materials School of Chemistry Dalian University of Technology State Key laboratory of Chemical Resource Engineering College of Chemical Engineering Beijing University of Chemical Technology

Intrinsic topological defect engineering has been proven as a promising strategy to elevate the electrocatalytic activity of carbon materials. However, the controllable construction of high-density and specific topological defects in carbon frameworks to reveal the relationship between reactivity and defect structure remains a challenging task. Herein, the intrinsic pentagon carbon sites that can favor electron overflow and enhance their binding affinity towards the intermediates of catalytic reaction are firstly presented by the work function and the p-band center calculations. To experimentally verify this, the cage-opening reaction of fullerene is proposed and utilized for synthesizing carbon quantum dots with specific pentagon configuration(CQDs-P), subsequently utilizing CQDs-P to modulate the micro-scale defect density of three-dimensional reduced graphene oxide(rGO) via π-π interactions. The multiple spatial-scale rGO-conjugated CQDs-P structure simultaneously possesses abundant pentagon and edge defects as catalytic active sites and long-range-ordered π electron delocalization system as conductive network. The defects-rich CQDs-P/rGO-4 all-carbon-based catalyst exhibits superb catalytic activity for triiodide reduction reaction with a high photoelectric conversion efficiency of 8.40%, superior to the Pt reference(7.97%). Theoretical calculations suggest that pentagon defects in the carbon frameworks can promote charge transfer and modulate the adsorption/dissociation behavior of the reaction intermediates, thus enhancing the electrocatalytic activity of the catalyst. This work confirms the role of intrinsic pentagon defects in catalytic reactions and provides a new insight into the synthesis of defects-rich carbon catalysts.

关键词： Carbon quantum dots Defect engineering Electrocatalytic activity Pentagon carbon Triiodide reduction

NaGd0.4Eu0.6Mg1-xZnxWO6 solid solution red phosphors:Microstructure variation and luminescence enhancement induced by Zn2+-doping

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Journal of Rare Earths 2024年第7期42卷 1224-1232页

作者： Yu Gao Jiayang Liao Mingyi Zhang Qingmei Tang Ting Zhou Mengjiao Liu Yan Zhao Xin Lai Daojiang Gao College of chemistry and materials Science Sichuan Normal University

Red phosphor is an important component of the phosphor-converted white light-emitting diodes（pcWLEDs）.The development of the novel red phosphor with excellent luminescence properties is of great significance for high performance WLEDs.In this study,NaGd0.4Eu0.6Mg1-xZnxWO6red phosphors with excellent luminescence properties were successfully synthesized and systematically investigated.Our results show that the Zn2+-doping concentration has significant effect on the microstructures and luminescence properties of the NaGd0.4Eu0.6Mg1-xZnxWO6phosphors.The NaGd0.4Eu0.6Mg1-xZnxWO6（0≤x≤0.7） samples are well crystallized pure solid solution sub-microcrystals,whereas the phase purity gradually decreases at 0.70.4Eu0.6Mg1-xZnxWO6（00.4Eu0.6MgWO6,and the optimized NaGd0.4Eu0.6Mg0.9Zn0.1WO6phosphor possesses the best luminescence properties including thermal stability,CIE chromaticity coordinate,life time and quantum yield.The packaged WLED using NaGd0.4Eu0.6Mg0.9Zn0.1WO6phosphor emits bright white light with higher CRI,lower CCT,and chromaticity coordinate close to the pure white light.The developed NaGd0.4Eu0.6Mg1-xZnxWO6phosphors have potential application in lighting and display.This work can offer an effective strategy for boosting luminescence properties of tungstate phosphors with the double perovskite structure.

关键词： Double perovskite Luminescence Microstructure Rare earths Tungstate phosphor Zn2+-doping