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Mg-doped,carbon-coated,and prelithiated SiO_(x) as anode materials with improved initial Coulombic efficiency for lithium-ion batteries

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Carbon Energy 2024年第3期6卷 204-214页

作者： Bin Liu Jie Liu Cheng Zhong wenbin hu Key Laboratory of Advanced Ceramics and Machining Technology(Ministry of Education) School of Materials Science and EngineeringTianjin UniversityTianjinChina Tianjin Key Laboratory of Composite and Functional Materials School of Materials Science and EngineeringTianjin UniversityTianjinChina Joint School of National University of Singapore and Tianjin University TianjinChina International Campus of Tianjin University Binhai New CityFuzhouChina

Silicon suboxide(SiO_(x),x≈1)is promising in serving as an anode material for lithium-ion batteries with high capacity,but it has a low initial Coulombic efficiency(ICE)due to the irreversible formation of lithium silicates during the first cycle.In this work,we modify SiO_(x) by solid-phase Mg doping reaction using low-cost Mg powder as a reducing agent.We show that Mg reduces SiO_(2) in SiO_(x) to Si and forms MgSiO_(3) or Mg_(2)SiO_(4).The MgSiO_(3) or Mg_(2)SiO_(4) are mainly distributed on the surface of SiO_(x),which suppresses the irreversible lithium-ion loss and enhances the ICE of SiO_(x).However,the formation of MgSiO_(3) or Mg_(2)SiO_(4) also sacrifices the capacity of SiO_(x).Therefore,by controlling the reaction process between Mg and SiO_(x),we can tune the phase composition,proportion,and morphology of the Mg-doped SiO_(x) and manipulate the performance.We obtain samples with a capacity of 1226 mAh g^(–1) and an ICE of 84.12%,which show significant improvement over carbon-coated SiO_(x) without Mg doping.By the synergistical modification of both Mg doping and prelithiation,the capacity of SiO_(x) is further increased to 1477 mAh g^(–1) with a minimal compromise in the ICE(83.77%).

关键词： initial Coulombic efficiency lithium-ion batteries magnesium doping prelithiation silicon suboxide

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How the surface Cu layer affected the activity of Ni foil for alkaline hydrogen evolution

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Journal of Materials Science & Technology 2024年第2期169卷 11-18页

作者： Qingfeng hu Yuan Liu Xuerong Zheng Jinfeng Zhang Jiajun Wang Xiaopeng Han Yida Deng wenbin hu School of Materials Science and Engineering Key Laboratory of Advanced Ceramics and Machining Technology of Ministry of EducationTianjin UniversityTianjin 300072China State Key Laboratory of Marine Resource Utilization in South China Sea School of Materials Science and EngineeringHainan UniversityHaikou 570228China Joint School of National University of Singapore and Tianjin University International Campus of Tianjin UniversityBinhai New CityFuzhou 350207China

Synthesizing bimetallic nanomaterials,with noble metals as the surface layers and inert metals as the substrates,has been proven to be an effective way to reduce the use of noble metals with maintained catalytic activity.However,an atomic diffusion from the inert substrate to the surface during the long-term operation has been reported to significantly decrease the activity.In this work,a series of catalysis-inert Cu-coated Ni foil were fabricated through electrodeposition and their activities for alkaline hydrogen evolution were investigated.Notably,the Ni/Cu-60 sample showed a similar catalytic property with pure Ni foil and only a slight decrease in HER activity was observed.The X-ray photoelectron spectroscopy(XPS)results indicated a decreased electron concentration of Cu in Ni/Cu-60,and theoretical calculations further demonstrated the electron transfer between the Ni substrate and Cu layer.Our results reveal that a specific composition or structure of an inert metal layer might not significantly decrease the electrocatalytic activity of active metals.Moreover,there are more possibilities for the rational design of metal-based catalysts for electrocatalysis.

关键词： Bimetallic heterostructure Charge redistribution Water splitting Alkaline hydrogen evolution

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A universal and ultrafast method for fabricating a library of nanocellulose-supported metal nanoparticles

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Progress in Natural Science:Materials International 2024年第2期34卷 389-395页

作者： Ziyi Luo Xiaoyang Wang Baihua Cui Hao Luo Tao Zhang Jia Ding Yanan Chen Yida Deng wenbin hu School of Materials Science and Engineering Tianjin University Department of Chemistry National University of Singapore State Key Laboratory of Marine Resource Utilization in South China Sea School of Materials Science and Engineering Hainan University

Using nanocatalysts to catalyze water electrolysis for hydrogen production is an ideal solution to address the energy crisis.The most well-adopted fabrication methods for nanocatalysts are tube furnace annealing,Hydrothermal method,etc.,hardly satisfying the trade-off among coarsening,dispersity,and particle size due to mutual restrictions.Herein,a universal,ultrafast and facile cellulose nanometer whiskers-high temperature shock（CNWHTS） method was reported for fabricating a library of ultrafine metal nanoparticles with uniform dispersion and narrow size distribution.The metal-anchor functional groups in CNW（i.e.,-OH and-COOH） and the characteristics of the HTS method for ultrafast heating and powerful quenching synergistically contribute to the successful synthesis of metal nanoparticles.As an initial demonstration,the as-prepared Pt nanocatalyst(η10 mA cm-2=51.8 mV) shows more excellent catalytic hydrogen evolution reaction（HER） performance than the Pt catalyst prepared in the tubular furnace(η10 mA cm-2=169.4 mV).This rapid and universal CNW-HTS method can pave the way for nanomanufacturing to produce high-quality metal nanoparticles,thereby expanding applications of energy conversion and electrocatalysis.

关键词： Electrocatalysis High-temperature shock Hydrogen evolution reaction (HER) Nanocellulose Nanomanufacturing Nanoparticles

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Boosting cycling stability by regulating surface oxygen vacancies of LNMO by rapid calcination

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Nano Research 2024年第4期17卷 2671-2677页

作者： Haoran Jiang Cuihua Zeng Wei Zhu Jiawei Luo Zhedong Liu Jingchao Zhang Rui Liu Yunhua Xu Yanan Chen wenbin hu School of Materials Science and Engineering Tianjin UniversityTianjin 300072China School of Materials Science and Engineering Shandong University of Science and TechnologyQingdao 266590China

Spinel LiNi_(0.5-x)Mn_(1.5+x)O_(4)(LNMO)has attracted intensive interest for lithium-ion battery due to its high voltage and high energy density.However,severe capacity fade attributed to unstable surface structure has hampered its commercialization.Oxygen vacancies(OVs)tend to occur in the surface of the material and lead to surface structure reconstruction,which deteriorates the battery performance during electrochemical cycling.Here,we utilize high-temperature-shock(HTS)method to synthesize LNMO materials with fewer surface OVs.Rapid calcination drives lower surface OVs concentration,reducing the content of Mn^(3+)and surface reconstruction layers,which is beneficial to obtain a stable crystal structure.The LNMO material synthesized by HTS method delivers an initial capacity of 127 mAh·g^(-1) at 0.1 C and capacity retention of 81.6%after 300 cycles at 1 C,and exhibits excellent performance at low temperature.

关键词： ultrafast synthesis oxygen vacancy LiNi_(0.5-x)Mn_(1.5+x)O_(4)(LNMO)cathode high-temperature-shock lithium-ion batteries

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Correlating the crystal structure and facet of indium oxides with their activities for CO_(2)electroreduction

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Fundamental Research 2024年第3期4卷 635-641页

作者： Jiajun Wang Guangjin Wang Han Wu Fei Liu Xixi Ren Yidu Wang Yanhui Cao Qi Lu Xuerong Zheng Xiaopeng Han Yida Deng wenbin hu School of Materials Science and Engineering Key Laboratory of Advanced Ceramics and Machining Technology of Ministry of EducationTianjin UniversityTianjin 300072China School of Materials Science and Energy Engineering Foshan UniversityFoshan 528000China State Key Laboratory of Marine Resource Utilization in South China Sea School of Materials Science and EngineeringHainan UniversityHaikou 570228China Joint School of National University of Singapore and Tianjin University International Campus of Tianjin UniversityBinhai New CityFuzhou 350207China

Constructing structure-function relationships is critical for the rational design and development of efficient catalysts for CO2 electroreduction reaction(CO2RR).In2O3 is well-known for its specific ability to produce formic acid.However,how the crystal phase and surface affect the CO_(2)RR activity is still unclear,making it difficult to further improve the intrinsic activity and screen for the most active structure.In this work,cubic and hexagonal In_(2)O_(3) with different stable surfaces((111)and(110)for cubic,(120)and(104)for hexagonal)are investigated for CO_(2)RR.Theoretical results demonstrate that the adsorption of reactants on cubic In_(2)O_(3) is stronger than that on hexagonal In_(2)O_(3),with the cubic(111)surface being the most active for CO_(2)RR.In experiments,synthesized cubic In_(2)O_(3) nanosheets with predominantly exposed(111)surfaces exhibited a high HCOO^(-)Faradaic efficiency(87.5%)and HCOO^(–)current density(–16.7 mA cm^(-2))at–0.9 V vs RHE.In addition,an aqueous Zn-CO_(2) battery based on a cubic In2O3 cathode was assembled.Our work correlates the phases and surfaces with the CO_(2)RR activity,and provides a fundamental understanding of the structure-function relationship of In_(2)O_(3),thereby contributing to further improvements in its CO_(2)RR activity.Moreover,the results provide a principle for the directional preparation of materials with optimal phases and surfaces for efficient electrocatalysis.

关键词： Structure-function relationship CO_(2)electroreduction Indium oxide Reactionmechanism Catalyst design

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Photocatalyzed ditrifluoromethylthiolation of alkenes with CF_(3)SO_(2)Na

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Science China Chemistry 2024年第2期67卷 587-594页

作者： Fangming Chen Lvqi Jiang Chunyang hu Jie Liu wenbin Yi School of Chemistry and Chemical Engineering Nanjing University of Science and TechnologyNanjing210094China Key Laboratory of Organofluorine Chemistry Shanghai Institute Organic ChemistryChinese Academy of SciencesShanghai200032China

Since the first report of sodium trifluoromethanesulfinate(CF_(3)SO_(2)Na) as an electrophilic trifluoromethylthiolation reagent in 2015,there has been no breakthrough in research in this field.Herein,we disclose an unprecedented usage of CF_(3)SO_(2)Na as a radical trifluoromethylthiolation reagent.A photocatalyzed ditrifluoromethylthiolation of alkenes with CF_(3)SO_(2)Na in the presence of PPh_(3) and catalytic copper has been developed.Interestingly,either Ir[(p-Fppy)_(2)(bpy)]PF_6 or Ir(ppy)_(3) could facilitate this transformation.Mechanistic studies indicate that initiation of the radical chain proceeded via two different photocatalytic quenching mechanisms.This protocol provides a practical method for the construction of diverse vicinal ditrifluoromethylthiolated compounds.

关键词： trifluoromethylthiolation photocatalysis radical difunctionalization alkenes

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High-entropy oxide-supported platinum nanoparticles for efficient hydrogen evolution reaction

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Rare Metals 2024年第4期43卷 1537-1546页

作者： Ming-Yu Fan Jia-Jun Wang Jun Zhao Hong Zhang Tian-Yi Ma Xiao-Peng Han Wen-Bin hu School of Materials Science and Engineering Tianjin Key Laboratory of Composite and Functional Materials Key Laboratory of Advanced Ceramics and Machining Technology Tianjin University School of National University of Singapore and Tianjin University International Campus of Tianjin University School of Science RMIT University

High-entropy oxides（HEOs） are a new class of single-phase structures with unique electronic and catalytic properties;therefore,it is worthwhile to explore their applications in electrocatalysis.In this study,a Pt/（FeCoNiCrAl）3O4nanohybrid using HEO as a support was developed as an efficient catalyst for the hydrogen evolution reaction（HER）.Pt/（FeCoNiCrAl）3O4exhibited high HER activity with a low overpotential of 22 mV at10 mA·cm-2,outperforming other binary,ternary,and quaternary supports.The HER activity of Pt/（FeCoNiCrAl）3O4was higher than that of a commercial Pt/C with a significantly lower Pt loading.The catalyst exhibited good activity and long-term stability（60 h） in an electrolytic water-splitting device.This good activity can be attributed to the fact that the introduction of Pt effectively facilitates electronic interactions between Pt and the HEO.In addition,the HEO substrate was more favorable for dispersing Pt particles,optimizing the electrochemical specific surface area,and significantly reducing the charge resistance of the HER.This study extends the application of HEOs in electrocatalysis and demonstrates the promising prospects of HEOs as supports for electrocatalysts.

关键词： High-entropy oxides Hydrogen evolution reaction Nanohybrid Water electrolysis

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Reversible Zn stripping/plating achieved by surface thin Sn layer for high-performance aqueous zinc metal batteries

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Journal of Materials Science & Technology 2022年第22期117卷 72-78页

作者： Bingfeng Cui Yu Gao Xiaopeng Han wenbin hu Tianjin Key Laboratory of Composite and Functional Materials Key Laboratory of Advanced Ceramics and Machining Technology(Ministry of Education)School of Materials Science and EngineeringTianjin UniversityTianjin 300350China

Aqueous zinc metal batteries (ZMBs) are considered as the most promising candidate for large-scale energy storage system due to their abundant reserves and high safety. To achieve highly stable zinc metalbatteries, it is imperative to inhibit the unavoidable dendrite growth, which leads to the non-uniformzinc deposition and even makes the battery short circuit. Herein, Sn coating is loaded on copper foil(SCF) by a simple electrodeposition to guide the uniform zinc deposition, which not only lowers the zincnucleation overpotential but also promotes the uniform zinc deposition/dissolution. As a result, the Znplated SCF (Zn@SCF) anode presents a low voltage hysteresis of ∼40 mV and a superior stability over270 h in symmetric cells at a current density of 1 mA cm^(−2). Furthermore, the Zn@SCF anode can realizethe improved performance for full cells paired with α-MnO_(2) cathode. This work provides a simple andeffective approach to modify the Zn anode for improved electrochemical performance of ZMBs.

关键词： Tin coatings Uniform zinc deposition Zinc anode Zinc metal batteries

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A chromosome-level genome assembly for Chinese plum‘Wushancuili'reveals the molecular basis of its fruit color and susceptibility to rain-cracking

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Horticultural Plant Journal 2024年第3期10卷 672-688页

作者： Kun Zhou Jingwen Wang Lin Pan Fang Xiang Yi Zhou Wei Xiong Ming Zeng Donald Grierson wenbin Kong Lingyu hu Wanpeng Xi College of Horticulture and Landscape Architecture Southwest UniversityChongqing 400715China Key Laboratory of Agricultural Biosafety and Green Production of Upper Yangtze River(Ministry of Education) Southwest UniversityChongqing 400715China Department of Pomology Chongqing Agricultural Technology Extension StationChongqing 401420China Plant and Crop Sciences Division School of BiosciencesUniversity of NottinghamSutton Bonington CampusLoughborough LE125RDUK Wuxi Economical Crop Technology Extension Station Chongqing 405800China

Chinese plum(Prunus salicina Lindl.)originates from China and makes a large contribution to the global production of plums.The P.salicina‘Wushancuili'has a green coloration and high fruit quality and is economically important in eliminating poverty and protecting ecology in the Yangtze River Three Gorges Reservoir.However,rain-induced cracking(rain-cracking,literally skin cracking caused by rain)is a limitation to‘Wushancuili'fruit production and causes severe losses.This study reported a high-quality‘Wushancuili'genome assembly consisting of a 302.17-Mb sequence with eight pseudo-chromosomes and a contig N50 of 23.59 Mb through the combination of Illumina sequencing,Pacific Biosciences HiFiⅢsequencing,and high-throughput chromosome conformation capture technology.A total of 25109 protein-coding genes are predicted and 54.17%of the genome is composed of repetitive sequences.‘Wushancuili'underwent a remarkable orthoselection during evolution.Gene identification revealed that loss-of-function in four core MYB10 genes results in the anthocyanin deficiency and absence of red color,revealing the green coloration due to the residual high chlorophyll in fruit skin.Besides,the occurrence of cracking is assumed to be closely associated with cell wall modification and frequently rain-induced pathogen enrichment through transcriptomic analysis.The loss of MYB10 genes might render fruit more susceptible to pathogen-mediated cracking by weakening the epidermal strength and reactive oxygen species(ROS)scavenging.Our findings provided fundamental knowledge regarding fruit coloration and rain-cracking and will facilitate genetic improvement and cultivation management in Chinese plums.

关键词： Chinese plum Fruit coloration Fruit epidermis Genome MYB10 Rain-cracking

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Exploiting H-induced lattice expansion in β-palladium hydride for enhanced catalytic activities toward oxygen reduction reaction

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Journal of Materials Science & Technology 2022年第3期98卷 205-211页

作者： Yunwei Liu Zelin Chen Chang Liu Jinfeng Zhang wenbin hu Yida Deng Tianjin Key Laboratory of Composite and Functional Materials School of Materials Science and EngineeringTianjin UniversityTianjin 300372China State Key Laboratory of Marine Resource Utilization in South China Sea School of Materials Science and EngineeringHainan UniversityHaikou 570228China

We have developed an efficient strategy to synthesize an active and durable electrocatalyst of Pd hydride nanocubes(NCs).Instead of the traditional chemical method,the PdH_(0.43)NCs are firstly prepared via a hydrogen diffusion procedure,followed by hydrothermal synthesis of an amorphous CuO layer encapsulating the PdH_(0.43)NCs to prevent the hydrogen atoms from escaping.Obvious lattice expansion is demonstrated playing a pivotal role in the enhancement of their oxygen reduction reaction(ORR)activity and durability.The obtained PdH_(0.43)@CuO NCs catalysts exhibit an ORR mass activity of 0.18 A mg^(−1) at 0.90 V versus reversible hydrogen electrode in an alkaline medium,which is about five times higher than that of commercial Pt/C.Accelerated durability tests show that there is only a 32 mV decay in halfwave potential even after 10,000 potential cycles,indicating the excellent stability of PdH_(0.43)@CuO NCs.Density functional theory(DFT)calculations also indicate that,compared to Pd,PdH_(0.43)has a lower limiting barrier to form OH−during the ORR process.The present study illustrates the importance of lattice expansion caused by hydrogen and offers an available strategy to design highly efficient and durable Pdbased electrocatalysts for alkaline fuel cells.

关键词： Lattice expansion Pd hydride Amorphous CuO Elecrocatalysis Oxygen reduction reaction

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