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Polyphenol Synergistic Cerium Oxide Surface Engineering Constructed Core-Shell Nanostructures as Antioxidants for Durable and High-Performance Proton Exchange Membrane Fuel Cells

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SSRN 2023年

作者： Tang, Haolin Zhao, Shengqiu Liao, Yucong Wang, Rui Liu, Guoliang Zhang, Haining State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory The Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

The chemical degradation of proton exchange membranes (PEMs) suffering from radical attack is a crucial issue in the development of proton exchange membrane fuel cells (PEMFCs), while incorporating cerium oxide (CeO2) nanoparticles (NPs) with regenerative redox properties to eliminate radicals could effectively alleviate degradation. However, the low stability and restricted activity of CeO2 in the PEMFC operating condition and the poor compatibility with PEM due to CeO2 agglomeration stimulate the urgency for structural modulation of CeO2. Herein, polyphenols surface functionalized CeO2 core-shell structure (CeO2@TP) were constructed via assembling oxidation-induced coupling tea polyphenols (TP) on CeO2 NPs. The TP oligomeric shell as a protective layer enhances the stability of CeO2, mitigating radical scavenging activity degradation and improving compatibility with PEMs. Gratifyingly, the phenolic hydroxyl-rich reductive TP oligomeric shell accelerates the regeneration of Ce(IV) to Ce(III), increasing the proportion of Ce(III) and oxygen vacancies on the CeO2 surface, thus boosting antioxidation efficiency. As a result, the CeO2@TP-based PEMs exhibited an OCV decay rate of 0.22 mV h-1, a maximum power density of 1.06 W cm-2, an H2 crossover value of 2.18 mA cm-2, thickness retention (91.1%), and negligible Ce migration after 404 hours of accelerated degradation testing. © 2023, The Authors. All rights reserved.

关键词： Oligomers

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Electrical Properties and Degradation Behavior of Bnt-Bt-Ln Ceramics

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SSRN 2023年

作者： Xu, Qi Yan, Xuerui He, Xin Dong, Shengde Ma, Luxiang Hai, Chunxi Zhou, Yuan Liu, Hanxing College of Materials and Chemistry & Chemical Engineering Chengdu University of Technology Chengdu610059 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Material Science and Engineering Wuhan University of Technology Wuhan430070 China

Dielectric capacitors are widely used in pulse power systems, electric vehicles, aerospace and defense technology as critical electronic components. Due to the miniaturization and diversification of electronic components, higher requirements are put on the electrical properties and the service life of dielectric capacitors. In this paper, the phase structure, microstructure, dielectric, ferroelectric and failure behavior of (1-x)(Bi0.5Na0.5TiO3-BaTiO3)-xLiNbO3 (BNT-BT-LN, x = 0.01, 0.03, 0.05, 0.07, 0.10) lead-free ceramics were investigated. All the samples exhibited perovskite phase with no secondary impurity. With increasing LiNbO3 concentration, the average grain size gradually increases from 0.78 μm to 1.75 μm. For the composition x = 0.07, the temperature coefficient of capacitance (TCC150°C) was lower than 15% in the range of 35 °C - 400 °C with moderate permittivity (Εr 150 °C = 2050) and low dielectric loss (tanδ150 °C = 0.005). The RC constant is above 19.3 s up to 245 °C. Through Highly Accelerated Life Test (HALT), the mean time to failure (TTF) empirical formula for BNT-BT-LN dielectrics is established. It indicates that the degradation of the insulation resistance process is caused by the electromigration of oxygen vacancies and the TTF is predicted to reach 4.67×106 h at 7 kV/mm and room temperature. © 2023, The Authors. All rights reserved.

关键词： Lithium compounds

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Confined Tuning of the Charge Distribution of Pt Electrocatalyst for Reinforcing Anti-Poisoning Ability: Toward Efficient Separation of Hydrogen from Gases Containing Ammonia

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SSRN 2023年

作者： Jin, Changqing Wu, Fanglin Tang, Haibo Pan, Hongfei Chen, Zhida Wang, Rui Meng, Zihan Li, Junsheng Tang, Haolin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Foshan Xianhu Laboratory of the Advanced Energy Science Technology Guangdong Laboratory Xianhu Hydrogen Valley Foshan528200 China

The development of catalysts for hydrogen oxidation reaction (HOR) with enhanced resistance to ammonia poisoning is an important factor in the practical application of hydrogen electrochemical purification devices (HEPDs). This paper reports on the creation of a highly active and anti-ammonia HOR catalyst developed by tuning the charge distribution of the support material through nitrogen-doping of carbon. The nitrogen-doped carbon-supported platinum catalyst (Pt-N2/KB, 2.03 wt.% Pt) achieves a high mass activity and exchange current density of 2788 mA mgpt-1 and 1020 mA mgpt-1, respectively, which are 5.4 and 4.7 times higher than that of the comm. 20% Pt/C. The Pt-N2/KB catalyst also displays a lower percentage of current decay and enhanced electrochemical stability, indicating superior anti-ammonia toxicity in the tests with HEPD. Density functional theory (DFT) calculations reveal that the hydrogen adsorption free energy (ΔGH*) on the surface of Pt-N2/KB is close to zero and has a lower ammonia adsorption energy, thus accounting for its superior HOR activity and anti- ammonia poisoning ability. Consequently, this work facilitates the implementation of HOR catalysts for anti-ammonia poisoning in the HEPDs, thus accelerating the advancement of ammonia cracking for hydrogen production. © 2023, The Authors. All rights reserved.

关键词： Ammonia

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advanced Li-SexSy battery system:Electrodes and electrolytes

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Journal of materials Science & technology 2020年第20期52卷 1-15页

作者： Huan Du Shihao Feng Wen Luo Liang Zhou Liqiang Mai State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China Department of Physics School of ScienceWuhan University of TechnologyWuhan430070China

The worldwide energy shortage has led to numerous researches for the exploration of new-type battery materials to deal with the energy *** achieve a great leap in energy density,the study of high capacity electrode materials plays a major *** a replacement to the energy accumulation system of lithium-sulfur(Li-S) and lithium-selenium(Li-Se) batteries,great concern is generated over lithium/selenium-sulfur(Li-SexSy) batteries as they combine the advantages of S(high capacity) and Se(improved electrical conductivity),consequently stands for extensive new cathode *** recent years,widespread researches have been conducted and great achievements have been *** review sums up the research status on Li-SexSy batteries and concentrates on the outstanding work of SexSy cathode *** reaction mechanism and capacity fading mechanism are *** performance-structure relationship is stated in regard of different cathode structures,including a variety of carbon hosts,conducting polymer hosts,transition metal-doped carbon electrodes and various Se/S *** compatibilities of frequently-used carbonate-based and ether-based electrolyte and other new-type electrolytes for Li-SexSy battery are *** for the future developments of Li-SexSy batteries are finally proposed.

关键词： Selenium-sulfur Cathode materials Electrolytes Lithium-sulfur

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Zero-Valent Iron Supported by Dendritic Mesoporous Silica Nanoparticles to Purify Dye Wastewater

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SSRN 2023年

作者： Chang, Baisong Dong, Kangfeng Wu, Shaolong Sun, Taolei State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China School of Chemistry Chemical Engineering and Life Science Wuhan University of Technology Wuhan430070 China

The presence of different types of organic dyes in water stream will clearly give rise to unexceptional side effects on living organisms. Emerging physical or chemical methods have been developed for the treatment of dye-involving water, but the exploration for adequate design strategy and technique available is still ongoing. Here, the zero-valent iron (ZVI) was prepared by a liquid phase sodium borohydride reduction approach and then integrated with dendritic mesoporous silica nanoparticle (DMSN) to construct the Janus magnetic adsorbent (denoted as ZVI-DMSN), which could be employed to purify dye wastewater. The structure, magnetic properties and dye adsorption results of ZVI-DMSN were systematically investigated. The ZVI component can enable efficient solid-liquid separation through magnetic separation route, and, more importantly, provided additional binding sites for adsorption process to increase the adsorption capacity. The thermodynamic analysis of adsorption indicated that the adsorption of typical organic dyes was an irreversible, spontaneous and endothermic process. Moreover, ZVI-DMSN adsorbent was recyclable, showing a regeneration efficiency of more than 80% after 5 cycles. We believe that ZVI-DMSN, as an inexpensive adsorbent material with excellent adsorption properties, e.g., short time, high efficiency and large capacity, will host vast potential for removal of dyes in water bodies. © 2023, The Authors. All rights reserved.

关键词： Wastewater treatment

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Domain Evolution, Dielectric and Piezoelectric Response in Bent Freestanding PbTiO3 Ferroelectric Nanowires

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SSRN 2024年

作者： Zhou, Meng-Jun Peng, Kun Tan, Yueze Yang, Tiannan Chen, Long-Qing Nan, Ce-Wen State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Center of Smart Materials and Devices School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China Department of Materials Science and Engineering Materials Research Institute The Pennsylvania State University University ParkPA16802 United States School of Mechanical Engineering Shanghai Jiao Tong University Shanghai200240 China School of Materials Science and Engineering State Key Lab of New Ceramics and Fine Processing Tsinghua University Beijing100084 China

Ferroelectric oxides with excellent flexibility are of significant practical and theoretical interests in recent studies. With most up-to-date research efforts, the effect of large bending on properties of nano-scale ferroelectric materials is still to be investigated. In this work, we elucidate the effect of bending angle on ferroelectric domain structures and material properties of bending PbTiO3 nanowires using phase-field simulations and thermodynamic modeling. We find non-monotonic dependencies of the coercive fields, dielectric responses and piezoelectric properties on the bending angle. A maximum enhancement of 462% and 226% in the dielectric constant and piezoelectric coefficient, respectively, is achieved at an 18° bending angle for the PbTiO3 nanowire with a radius of R = 10 nm and length L=100 nm, which is attributed to the formation of strong-response zones within the nanowire as illustrated by both the phase-field and thermodynamic analysis. The current work provides useful theoretical insights for the experimental explorations into ferroelectric functionalities of nanomaterials and potential applications of high-performance flexible ferroelectric-based nanodevices. © 2024, The Authors. All rights reserved.

关键词： Piezoelectricity

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Binder-free electrodes for advanced potassium-ion batteries:A review

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Chinese Chemical Letters 2021年第4期32卷 1299-1308页

作者： Wencong Liu Wenyi Liu Yuqi Jiang Qiuyue Gui Deliang Ba Yuanyuan Li Jinping Liu School of Chemistry Chemical Engineering and Life ScienceState Key Laboratory of Advanced Technology for Materials Synthesis and ProcessingWuhan University of TechnologyWuhan 430070China School of Optical and Electronic Information Huazhong University of Science and TechnologyWuhan 430074China Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of EducationSchool of Physics and Electronic EngineeringHarbin Normal University.Harbin 150025China

Potassium-ion batteries(PIBs)have attracted enormous attention due to the abundance of potassium resources,low cost,fast ionic conductivity of electrolyte and relatively high operating *** great effo rts and progress,researches on PIBs are still at the initial stage,especially in the emerging field of flexible and wearable *** inevitable challenges for PIBs include low reversible capacity,unsatisfactory cycling stability and insufficient energy density,the solution to which mostly relies on designing adva nced ***-free electrodes have emerged as promising electrode architecture for *** electrodes avoid the use of insulating binders,which can be designed with various synergistic functional materials to address the aforementioned PIB issues and be endowed with flexibility/*** this review,we mainly summarize the recent progress on binde r-free electrodes for PIBs,with the focus on the methodologies,detailed strategies and functional materials for electrode *** strategy for binder-free electrodes is to assemble free-standing architecture with the help of carbon nanotubes(CNTs),graphitic fibers,and other carbon or mechanically robust materials,either alone or in *** other effective strategy is current collector substrate-assisted direct growth,including the use of carbon cloth,*** and other conductive ***,challenges and research opportunities are put forward at the end as the guidance for future development of binder-free PIB devices.

关键词： Binder-free Free-standing electrode Substrate-assisted directly grown electrode Potassium-ion battery Flexible device

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Rational synthesis of Cylindrical Silver Single-crystalline Nanowires via Poly(vinyl pyrrolidone) Reduction of AgCl

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Journal of Wuhan University of technology(materials Science) 2020年第3期35卷 473-481页

作者： DUAN Junyuan YANG Rui HAN Meng LIU Bingxin WANG Yilong GUAN Jianguo State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Mechanical Engineering Qinghai UniversityXining 810016China

We presented a simple yet convenient hydrothermal approach for the large-scale synthesis of uniform cylindrical silver (Ag) single-crystalline nanowires with diameters of about 25 nm and lengths of 1-4 μm. Poly(vinyl pyrrolidone) (PVP) was used as a reducing agent, and AgCl was used as a precursor to deliberately control [Ag^+] at a low degree in the overall reaction process through its dynamic equilibrium by directly reducing AgCl with PVP at a quasi-equilibrium growth condition. The as-obtained products were characterized by powder X-ray diffraction (XRD) patterns, field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), infrared spectra (IR) and Raman spectra. Factors such as [PVP], reaction temperature, time, and species of reducing agents and precursors were investigated to have strong influences on the morphologies and structures of the resultant Ag nanostructures. The wire diameter can conveniently be adjusted between 25 and 50 nm by simply adjusting [PVP], reaction temperature and reducing agent species. The as-synthesized silver nanowires can be self-assembled into perfect order arrays after being dried on tin foil due to the PVP coating on the surface, the circular cross-section and the uniform diameter of the Ag nanowires. These special silver nanowires with a core-shell structure as well as their spontaneous self-assembly of order arrays are expected to provide potential applications in flexible conductors, dielectric materials, electromagnetic shielding materials and nano-devices.

关键词： silver nanowires poly(vinyl pyrrolidone) hydrothermal approach self-assembly

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NaTiOx-modified high-nickel layered oxide cathode for stable sodium-ion batteries

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Carbon Energy 2025年第01期 287-295页

作者： Yingcong Liu Xing Zhou Dongwei He Xiaowei Liu Chao Yang Dawei Xu Meilong Wang Ruitao Sun Bin Zhang Jingjing Xie Jin Han Wen Chen Ya You State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Yibin Libode New Materials Co.Ltd International School of Materials Science and Engineering School of Materials Science and Microelectronics Wuhan University of Technology

The O3-type layered cathode with high Ni content has attracted much attention because of its high capacity and simple synthesis ***,surface side reaction and O3-P3 phase transitions would occur during Na+insertion/extraction,resulting in unsatisfying electrochemical ***,O3-Na[Ni0.6Co0.2Mn0.2]O2（NNCM622） cathode is modified by a NaTiOxcoating layer in a wet chemistry method,which reduces the parasitic reaction and facilitates Na+***,the partially doped Ti improves structural stability by restraining the irreversible multiple-phase *** a result,the modified NNCM622 cathode obtains a high specific capacity of 143.4mAhg-1and an improved capacity retention of 69% after300 *** work offers new prospects for stabilizing the NNCM622cathode with a feasible coating strategy.

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A new catalyst for urea oxidation: NiCo2S4 nanowires modified 3D carbon sponge

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Journal of Energy Chemistry 2020年第11期29卷 195-205页

作者： Biaopeng Li Congying Song Jianjun Rong Jing Zhao Hong-En Wang Ping Yang Ke Ye Kui Cheng Kai Zhu Jun Yan Dianxue Cao Guiling Wang Key Laboratory of Superlight Materials and Surface Technology of Ministry of Education College of Materials Science and Chemical EngineeringHarbin Engineering UniversityHarbin 150001HeilongjiangChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina

Urea oxidation is a significant reaction for utilizing urea-rich wastewater or human urine as sustainable power sources which can ease the water eutrophication while generate electricity. A direct urea-hydrogen peroxide fuel cell is a new kind of fuel cell employing urea as fuel and hydrogen peroxide as oxidant which possesses a larger cell voltage. Herein, this work tries to promote the kinetics process of urea oxidation by preparing low-cost and high-efficient NiCo2S4 nanowires modified carbon sponge electrode. The carbon sponge used in this work with a similar three-dimensional multi-channel structure to Ni foam, is prepared by carbonizing recycled polyurethane sponge which is also a process of recycling waste. The performance of the prepared catalyst in an alkaline solution is investigated in a three-electrode *** the introduction of Co element to the catalyst, a reduced initial urea oxidation potential and a high performance are obtained. Furthermore, a direct urea-hydrogen peroxide fuel cell is assembled using the NiCo2S4 nanowires modified carbon sponge anode. Results indicate that the prepared catalyst provides a chance to solve the current problems that hinder the development of urea electrooxidation(high initial urea oxidation potential, low performance, and high electrode costs).

关键词： Carbon sponge Direct urea fuel cell Electrocatalyst NiCo2S4 nanowires Urea oxidation

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