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Multi boron-doping effects in hard carbon toward enhanced sodium ion storage

Journal of Energy Chemistry 2025年第1期100卷 730-738页

作者： Peng Zheng Wang Zhou Ying Mo Biao Zheng Miaomiao Han Qin Zhong Wenwen Yang Peng Gao Lezhi Yang Jilei Liu College of Materials Science and Engineering Hunan Joint International Laboratory of Advanced Materials and Technology for Clean EnergyHunan Province Key Laboratory for Advanced Carbon Materials and Applied TechnologyHunan UniversityChangsha 410082HunanChina Greater Bay Area Institute for Innovation Hunan UniversityGuangzhou 511300GuangdongChina Changsha Research Institute of Mining&Metallurgy Co. LTD.Changsha 410017HunanChina

Hard carbon (HC) has been considered as promising anode material for sodium-ion batteries (SIBs).The optimization of hard carbon’s microstructure and solid electrolyte interface (SEI) property are demonstrated effective in enhancing the Na+storage capability,however,a one-step regulation strategy to achieve simultaneous multi-scale structures optimization is highly ***,we have systematically investigated the effects of boron doping on hard carbon’s microstructure and interface chemistry.A variety of structure characterizations show that appropriate amount of boron doping can increase the size of closed pores via rearrangement of carbon layers with improved graphitization degree,which provides more Na+storage ***-situ Fourier transform infrared spectroscopy/electrochemical impedance spectroscopy (FTIR/EIS) and X-ray photoelectron spectroscopy (XPS) analysis demonstrate the presence of more BC3and less B–C–O structures that result in enhanced ion diffusion kinetics and the formation of inorganic rich and robust SEI,which leads to facilitated charge transfer and excellent rate *** a result,the hard carbon anode with optimized boron doping content exhibits enhanced rate and cycling *** general,this work unravels the critical role of boron doping in optimizing the pore structure,interface chemistry and diffusion kinetics of hard carbon,which enables rational design of sodium-ion battery anode with enhanced Na+storage performance.

关键词： Hard carbon Sodium-ion batteries Boron doping Pore structure Electrode/electrolyte interphases

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Copper oxide-modified highly reversible Zn powder anode for aqueous Zn metal batteries

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Rare Metals 2024年第10期43卷 5005-5016页

作者： Guan-Qun Liu Biao Fu Zhe-Xuan Liu Lan-Yan Li Shu-Quan Liang Guo-Zhao Fang School of Materials Science and Engineering Key Laboratory of Electronic Packaging and Advanced Functional Materials of Hunan ProvinceCentral South UniversityChangsha 410083China School of Science Hunan University of Technology and BusinessChangsha 410205China National Energy Metal Resources and New Materials Key Laboratory Central South UniversityChangsha 410083China

With the advantages of mature preparation technology,structural adjustability and suitability for large-scale application,Zn powder anode is considered to be an ideal electrode for realizing low-cost,high-energy-density aqueous Zn metal ***,the high specific surface of Zn powders leads to severe side reactions such as hydrogen evolution and corrosion,thus limiting their widespread use Here,this work develops a novel CuO@Zn powder anode with a synergy effect of surface wrapping and *** powders are uniformly wrapped by small CuO particles due to the strong adsorption between Zn and *** wrapped CuO particles build a good conductive framework to inhibit the structural collapse of the Zn powder caused by corrosion and non-uniform ***,CuO can also be used as a seed to guide the uniform deposition of Zn ions through its strong binding energy with *** a result,the Cu O@Zn anode can maintain a long cyclic life of 900 h at current density of 1 mA·cm^(-2)and capacity of 1 mAh·cm^(-2),as well as contribute to an excellent capacity retention of 92% after 800cycles for CuO@Zn||NH_(4)V_(4)O_(10)full *** at high current density of 5 A·g^(-1),the full cell exhibits a specific capacity of more than 200 mAh·g^(-1)after 800 cycles,with a good capacity retention of 89%.This work provides a new idea for developing high-performance Zn powder-based anodes.

关键词： Zn powder Copper oxide surface wrapping Zn anode Aqueous Zn metal batteries

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Petroleum pitch derived hard carbon via NaCl-template as anode materials with high rate performance for sodium ion battery

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Frontiers of Chemical science and Engineering 2024年第7期18卷 1-10页

作者： Baoyu Wu Hao Sun Xiaoxue Li Yinyi Gao Tianzeng Bao Hongbin Wu Kai Zhu Dianxue Cao Key Laboratory of Superlight Materials and Surface Technology of Ministry of Education College of Materials Science and Chemical EngineeringHarbin Engineering UniversityHarbin 150001China Hunan Hongshan New Energy Technology Co. LtdYiyang 413000China

Sodium-ion batteries(SIBs)have garnered significant interest in energy storage due to their similar working mechanism to lithium ion batteries and abundant reserves of sodium *** facile synthesis of a carbon-based anode materials with capable electrochemical performance is key to promoting the practical application of *** this work,a combination of petroleum pitch and recyclable sodium chloride is selected as the carbon source and template to obtain hard carbon(HC)anode for *** times and temperatures are optimized by assessing the sodium ion storage behavior of different HC *** optimized HC exhibits a remarkable capacity of over 430 mAh·g^(-1) after undergoing full activation through 500 cycles at a density of current of 0.1 A·g^(-1).Furthermore,it demonstrates an initial discharge capacity of 276 mAh·g^(-1) at a density of current of 0.5 A·g^(-1).Meanwhile,the optimized HC shows a good capacity retention(170 mAh·g^(-1) after 750 cycles)and a remarkable rate ability(166 mAh·g^(-1) at 2 A·g^(-1)).The enhanced capacity is attributed to the suitable degree of graphitization and surface area,which improve the sodium ion transport and storage.

关键词： petroleum pitch hard carbon sodium-ion batteries high rate recyclable template

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Tuning surface reactivity towards high-performance hard carbon in Li/Na/K-ion batteries

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Journal of Energy Chemistry 2025年第4期103卷 27-36页

作者： Wang Zhou Dan Wang Ying Mo Rui Tang Peng Gao Miaomiao Han Shi Chen Keigo Wakabayashi Takeharu Yoshii Hirotomo Nishihara Jilei Liu College of Materials Science and Engineering Hunan Joint International Laboratory of Advanced Materials and Technology of Clean EnergyHunan Province Key Laboratory for Advanced Carbon Materials and Applied TechnologyHunan UniversityChangsha 410082HunanChina The Key Laboratory of Micro-nano Energy Materials and Application Technologies University of Hunan Province&College of Physics and Electronic EngineeringHengyang Normal UniversityHengyang 421002HunanChina Joint Key Laboratory of the Ministry of Education Institute of Applied Physics and Materials EngineeringUniversity of MacaoMacao 999078China Institute of Multidisciplinary Research for Advanced Materials Tohoku University2-1-1 KatahiraAoba-kuSendaiMiyagi 980-8577Japan Advanced Institute for Materials Research(WPI-AIMR) Tohoku University2-1-1 KatahiraAoba-kuSendaiMiyagi 980-8577Japan

Controlling surface chemistry is critically important for improving the initial Coulombic efficiency(ICE)and adsorption capacity of hard carbon anode used in Li/Na/K-ion ***,accurately identifying the types and concentrations of hydrogen/oxygen terminated functional groups(HTFG/OTFGs)and distinguishing their functionalities remain ***,we quantitatively investigated the surface chemistry on hard carbon via ultra-high temperature programed desorption measurements,and uncovered the role of HTFG/OTFGs in influencing ICE and adsorption capacity in Li/Na/K-ions *** C-H group is found to be dominant species on the surface of hard carbon,and presents a positive correlation with ICE values and adsorption *** low reactivity of C-H group with both electrolyte salt and solvent results in the formation of thinner and highly conducive solid electrolyte interphase(SEI)layer,which benefit for the enhanced ICE and improved Li/Na/K-ions diffusion across SEI ***,the pimping trapping effect of C-H groups allows the adsorbed Li/Na/K-ions to migrate into graphitic interlayer quickly,enhancing the slope *** fabricating a C-H group-rich surface chemistry on hard carbon,a high ICE value and satisfactory specific capacity have been *** findings enrich our understanding of the surface chemistry-induced interfacial reaction,which effectively guides the rational design of high-performance hard carbon.

关键词： Hard carbon surface chemistry C–H bond Initial coulombic efficiency Adsorption capacity

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Heterogeneous β-Co(OH)_(2)/Cu_(2)(OH)_(3)Cl bifunctional electrocatalyst for superior concurrent conversion of glycerol and nitrite

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Journal of Energy Chemistry 2025年第5期104卷 185-193页

作者： Mingdan Wang Pengzuo Chen Huigang Wang Yanying Zhao School of Chemistry and Chemical Engineering Key Laboratory of Surface&Interface Science of Polymer Materials of Zhejiang ProvinceZhejiang Sci-Tech UniversityHangzhou 310018ZhejiangChina Hangzhou Institute of Advanced Studies Zhejiang Normal UniversityHangzhou 311231ZhejiangChina

The electrochemical biomass valorization of industrial by-products or pollutants using renewable electricity offers significant promise for carbon ***,the huge challenges still exist in the development of efficient bifunctional ***,we put forward a high-efficiency coelectrolysis system by coupling the nitrite reduction reaction(NO_(2)RR)and the glycerol oxidation reaction(GOR)over a novel heterogeneous β-Co(OH)_(2)/Cu_(2)(OH)_(3)Cl ***β-Co(OH)_(2)/Cu_(2)(OH)_(3)Cl shows excellent bifunctional performance with high Faradaic efficiencies of formate(90.1%)and NH_(3)(91.9%)at cell voltage of 1.5 V,high yield rate of formate(89.6 mg h^(-1)cm^(-2))and NH_(3)(36.07 mg h^(-1)cm^(-2))at cell voltage of 1.9 V,and superior stability in an anion exchange membrane *** in-situ Raman result confirms the unique Co/Cu-based bimetallic synergistic sites of β-Co(OH)_(2)/Cu_(2)(OH)_(3)Cl towards superior GOR performance,while the operando Fourier transform infrared spectroscopy demonstrates the improved protonation kinetics of key intermediates and optimized water dissociation ability ofβ-Co(OH)_(2)/Cu_(2)(OH)_(3)Cl for high NO_(2)RR *** work illuminates alternative avenues to exploit the innovative and energy-saving technology for the co-production of high-added chemicals.

关键词： Heterogeneous catalyst β-Co(OH)_(2)/Cu_(2)(OH)_(3)Cl Bifunctional performance Nitrite reduction reaction Glycerol oxidation reaction

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Developing new Mg alloy as potential bone repair material via constructing weak anode nano-lamellar structure

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Journal of Magnesium and Alloys 2023年第1期11卷 154-175页

作者： Jinshu Xie Lele Wang Jinghuai Zhang Liwei Lu Zhi Zhang Yuying He Ruizhi Wu Key Laboratory of Superlight Material and Surface Technology Ministry of EducationCollege of Materials Science and Chemical EngineeringHarbin Engineering UniversityHarbin150001China School of Materials Science and Engineering Hunan University of Science and TechnologyXiangtan411201China

The mechanics-corrosion and strength-ductility tradeoffs of magnesium(Mg)alloys have limited their applications in fields such as orthopedic ***,a fine-grain structure consisting of weak anodic nano-lamellar solute-enriched stacking faults(SESFs)with the average thickness of 8 nm and spacing of 16 nm is constructed in an as-extruded Mg96.9Y1.2Ho1.2Zn0.6Zr0.1(at.%)alloy,obtaining a high yield strength(YS)of 370 MPa,an excellent elongation(EL)of 17%,and a low corrosion rate of 0.30 mm y−1(close to that of high-pure Mg)in a uniform corrosion *** scanning Kelvin probe force microscopy(SKPFM),one-dimensional nanostructured SESFs are identified as the weak anode(∼24 mV)for the first *** excellent corrosion resistance is mainly related to the weak anodic nature of SESFs and their nano-lamellar structure,leading to the more uniform potential distribution to weaken galvanic corrosion and the release of abundant Y^(3+)/Ho^(3+)from SESFs to form a more protective film with an outer Ca_(10)(PO_(4))_(6)(OH)_(2)/Y_(2)O_(3)/Ho_(2)O_(3) layer(thickness percentage of this layer:72.45%).For comparison,the as-cast alloy containing block 18R long period stacking ordered(LPSO)phase and the heat-treated alloy with fine lamellar 18R-LPSO phase(thickness:80 nm,spacing:120 nm)are also studied,and the characteristics of SESFs and 18R-LPSO phase,such as the weak anode nature of the former and the cathode nature of the latter(37-90 mV),are distinguished under the same alloy ***,we put forward the idea of designing Mg alloys with high mechanical and anti-corrosion properties by constructing"homogeneous potential strengthening microstructure",such as the weak anode nano-lamellar SESFs structure.

关键词： Mg alloys Corrosion Solute-enriched stacking faults LPSO structure SKPFM Hydroxyapatite

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Improving structure stability of single-crystalline Ni-rich cathode at high voltage by element gradient doping and interfacial modifcation

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Journal of Energy Chemistry 2025年第2期101卷 630-640,I0013页

作者： Ruijuan Wang Yixu Zhang Zhi Li Lei Wu Jiarui Chen Xiaolin Liu Hui Hu Hao Ding Shuang Cao Qiliang Wei Xianyou Wang National Base for International Science&Technology Cooperation of New Energy Equipment Energy Storage Materials and DevicesNational Local Joint Engineering Laboratory for Key Materials of New Energy Storage BatteryHunan Province Key Laboratory of Electrochemical Energy Storage&ConversionSchool of ChemistryXiangtan UniversityXiangtan 411105HunanChina Institute of Micro/Nano Materials and Devices Ningbo University of TechnologyNingbo 315211ZhejiangChina

Single-crystalline Ni-rich cathodes can provide high energy density and capacity retention rates for lithium-ion batteries(LIBs).However,single-crystalline Ni-rich cathodes experience severe transition metal dissolution,irreversible phase transitions,and reduced structural stability during prolonged cycling at high voltage,which will significantly hinder their practical ***,a Li4TeO5surface coating along with bulk Te-gradient doping strategy is proposed and developed to solve these issues for single-crystalline Ni-rich LiNi_(0.90)Co_(0.05)Mn_(0.05)O_(2)cathode(LTeO-1.0).It has been found that the bulk Te^(6+)gradient doping can lead to the formation of robust Te-O bonds that effectively inhibit H_(2)-H3 phase transformations and reinforce the lattice framework,and the in-situ Li4TeO5coating layer can act as a protective layer that suppresses the parasitic reactions and grain ***,the modified material exhibits a higher Young's modulus,which will be conducive to maintaining significant structural and electrochemical stability under high-voltage conditions,Especially,the LTeO-1.0 electrode shows the improved Li^(+)diffusion kinetics and thermodynamic stability as well as high capacity retention of 95.83%and 82.12%after 200 cycles at the cut-off voltage of 4.3 and 4,5 ***,the efficacious dualmodification strategy will definitely contribute to enhancing the structural and electrochemical stability of single-crystalline Ni-rich cathodes and developing their application in LIBs.

关键词： Single-crystalline Ni-rich cathode High cut-off voltage Material fragmentation Li_(4)TeO_(5)coating layer Te^(6+)doping

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In-situ regeneration of Bi^(0) active site to renew surface activation for long-term stable and efficient CO_(2)-to-formate electrosynthesis

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Journal of Energy Chemistry 2024年第12期99卷 703-711页

作者： Haichuan He Congcheng Yang Liu Deng Li Luo Yahui Jiang Liqiang Wang Yi Zhang Minghui Yang You-Nian Liu Hunan Provincial Key Laboratory of Micro&Nano Materials Interface Science College of Chemistry and Chemical EngineeringCentral South UniversityChangsha 410083HunanChina College of Material Chemistry and Chemical EngineeringHangzhou Normal UniversityHangzhou 311121ZhejiangChina Henan Province Industrial Technology Research Institute of Resources and Materials School of Material Science and EngineeringZhengzhou UniversityZhengzhou UniversityZhengzhou 450001HenanChina

CO_(2)-to-formate electrosynthesis with high selectivity and stability has been a long-sought ***,most catalysts undergo structural and valence state changes due to surface oxidation during operation or storage,resulting in decreased catalytic ***,we report a efficient and stable BiIn@Cu-foam electrode through the in-situ regeneration of Bi^(0) active sites to renew the surface *** electronic structure of Bi site can be regulated by introducing In,thereby enhancing the adsorption strength of**** optimized electrode exhibits over 90%FE_(formate)at a wide potential window(-0.9–-2.2 V),and formation rate for 3.15 mM cm^(-1)h^(-1).Especially,the electrode can maintain the high performance at continuously electrolysis for more than 300 h,or for more than 50 cycles,even repeated operation and storage for more than 2 *** work provides a promising candidate and new insight to construct industrially viable stable Bi-based catalyst for formate electrosynthesis.

关键词： In-situ regeneration Stability Formate Bismuth eCO_(2)RR

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In situ preparation of Ag@AgCl/Bio-veins composites and their photocatalytic activity and recyclability

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Frontiers of Chemical science and Engineering 2023年第7期17卷 906-917页

作者： Min Zou Chao Tan Zhengqiu Yuan Ming Wu Jian Jian Lei Zhang Yan Zhang Zhou Ma Hu Zhou School of Resource&Environment and Safety Engineering Hunan University of Science and TechnologyXiangtan 411201China Key Laboratory of Theoretical Organic Chemistry and Functional Molecules Ministry of EducationFunctional Film Materials Engineering Research Center of Hunan ProvinceHunan Provincial Key Laboratory of Advanced Materials for New Energy Storage and ConversionSchool of Chemistry and Chemical EngineeringHunan University of Science and TechnologyXiangtan 411201China School of Information and Electrical Engineering Hunan University of Science and TechnologyXiangtan 411201China

The industrial application of nano-photocatalysts in wastewater treatment has been severely restricted for a long time due to their difficult separation,poor reusability,and low *** this work,a facile strategy was proposed to enhance the photocatalytic activity and recovery performance of Ag@AgCl *** veins(Bio-veins)with a unique 3D porous construction were used as carriers for the in-situ growth of Ag@AgCl *** electron microscopy results showed that the Ag@AgCl nanoparticles were uniformly loaded on the surface and interior of the Bio-veins,and the size of the Ag@AgCl nanoparticles immobilized on the Bio-veins(50–300 nm)was significantly smaller than Ag@AgCl obtained by the co-precipitation method(1–3μm).The Bio-veins played a vital role in the photocatalysis reaction *** degradation efficiency of the Ag@AgCl/Bio-veins(CI4)was up to 3.50 times as high as pure Ag@***,the composites also exhibited excellent recyclability and stability under both visible and solar *** work provided a suitable strategy for nano-photocatalysts for practical application and may also offer new possibilities for the high-value utilization of biomass materials.

关键词： Ag@AgCl biological veins photocatalytic activity recyclability

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Regularly Tuning Quantum Interference in Single-Molecule Junctions through Systematic Substitution of Side Groups with Varied Electron Effects

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Chinese Journal of Chemistry 2024年第11期42卷 1217-1222页

作者： Xianjing Xie Yirong Zhang Junrui Zhang Xingyuan Cui Wei Liu Xunshan Liu Key Laboratory of Surface&Interface Science of Polymer Materials of Zhejiang Province School of Chemistry and Chemical EngineeringZhejiang Sci-Tech University928 Second StreetHangzhouZhejiang310018 China State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChinese Academy of SciencesChangchunJilin130022 China School of Materials Science and Engineering Nanjing University of Science and TechnologyNanjingJiangsu210094 China

Investigating the quantum interference effect in single molecules is essential to comprehensively understand the underlying mechanism of single-molecule charge *** this study,we employed the mother molecule m-OPE and introduced a series of side groups with various electronic effects at the 2-position of the central phenyl ring,creating four daughter m-OPE *** single molecular conductivities of these molecule wires were measured using the scanning tunneling microscope breaking junction *** findings demonstrate that the substitutions regularly modulate the destructive quantum interference occurring within the m-OPE *** combining optical and electrochemical investigations,along with density functional theory computations,we discover that the conductivity of the molecules corresponds to the electron-donating/withdrawing ability of the ***,by adjusting the electron structures of the molecular backbone,we can systematically tailor the destructive quantum interference in the m-OPE molecules.

关键词： Quantum interference Single-molecule junctions Electron effect substituents Charge transport Molecular devices

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