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Cobalt-Free BaFe_(0.6)Zr_(0.1)Y_(0.3)O_(3−δ)Oxygen Electrode for Reversible Protonic Ceramic Electrochemical Cells

Transactions of Tianjin University 2023年第6期29卷 444-452页

作者： Chenghao Yang Jin Li Ao Hu Jian Pu Bo Chi State Key Laboratory of Materials Processing and Die and Mould Technology School of Materials Science and EngineeringHuazhong University of Science and TechnologyWuhan 430074China Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials MOE Key Laboratory for the Green Preparation and Application of Functional MaterialsFaculty of Materials Science and EngineeringHubei UniversityWuhan 430062China MOE Key Laboratory of Material Chemistry for Energy Conversion and Storage Huazhong University of Science and TechnologyWuhan 430074China

Reversible protonic ceramic electrochemical cells(R-PCECs)are ideal,high-effi ciency devices that are environmentally friendly and have a modular *** paper studies BaFe_(0.6)Zr_(0.1)Y_(0.3)O_(3−δ)(BFZY3)as a cobalt-free perovskite oxygen electrode for high-performance R-PCECs where Y ions doping can increase the concentration of oxygen vacancies with a remarkable increase in catalytic *** cell with confi guration of Ni-BZCYYb/BZCYYb/BFZY3 demonstrated promising performance in dual modes of fuel cells(FCs)and electrolysis cells(ECs)at 650℃with low polarization resistance of 0.13Ωcm^(2),peak power density of 546.59 mW/cm^(2)in FC mode,and current density of−1.03 A/cm^(2)at 1.3 V in EC *** alternative operation between FC and EC modes for up to eight cycles with a total of 80 h suggests that the cell with BFZY3 is exceptionally stable and reversible over the long *** results indicated that BFZY3 has considerable potential as an air electrode material for R-PCECs,permitting effi cient oxygen reduction and water splitting.

关键词： Protonic ceramic cells Oxygen electrode Perovskite oxides Cobalt-free Oxygen vacancies

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Boosting Li-ion storage in Li2MnO_(3) by unequal-valent Ti4+-substitution and interlayer Li vacancies building

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Chinese Chemical Letters 2023年第4期34卷 564-569页

作者： Yu Tian Yuling Zhao Fanqi Meng Kaicheng Zhang Yanyuan Qi Yujie Zeng Congcong Cai Yuli Xiong Zelang Jian Yang Sun Lin Gu Wen Chena School of Materials Science and Engineering Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China School of Materials Shenzhen Campus of Sun Yat-sen UniversityShenzhen 518107China C Innovation Laboratory Contemporary Amperex Technology Ltd.(CATL)Ningde 352100China Institute of Physics Chinese Academy of SciencesBeijing 100190China Sanya Science and Education Innovation Park of Wuhan University of Technology Wuhan 430070China

Lithium rich layered oxide(LRLO) has been considered as one of the promising cathodes for lithium-ion batteries(LIBs). The high voltage and large capacity of LRLO depend on Li2MnO_(3)phase. To ameliorate the electrochemical performance of Li2MnO_(3), also written as Li(Li1/3Mn2/3)O_(2), we propose a strategy to substitute Mn4+and Li+in Mn/Li transition metal layer with Ti4+, which can stabilize the structure of Li2MnO_(3)by inhibiting the excessive oxidation of O_(2)-above 4.5 V. More significantly, the unequal-valent substitution brings about the emergence of interlayer Li vacancies, which can promote the Li-ion diffusion based on the enlarged interlayer and increase the capacity by activating the Mn3+/4+redox. We designed Li0.7[Li1/3Mn2/3]0.7Ti0.3O_(2)with high interlayer Li vacancies, which presents a high capacity(290 m Ah/g at 10 m A/g) and stable cycling performance(84% over 60 cycles at 50 m A/g). We predict that this strategy will be helpful to further improve the electrochemical performance of LRLOs.

关键词： Lithium-ion batteries Li2MnO_(3) Unequal-valent Ti4+-substitution Interlayer Li vacancies Activated Mn3+/4+redox

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分子间相互作用调控丝素蛋白/聚丙烯酰胺水凝胶的网络形貌和β片结晶,赋予水凝胶优异的黏附、应变和传感性能

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Science China materials 2024年第5期67卷 1533-1542页

作者：杨德桢孙传强韩哲袁宝刚潘栋陈金传许华杰刘春太申长雨 State Key Laboratory of Structural Analysis Optimization and CAE Software for Industrial EquipmentNational Engineering Research Center for Advanced Polymer Processing Technologythe Key Laboratory of Advanced Materials Processing&Mold of Ministry of EducationZhengzhou UniversityZhengzhou450002China

丝素蛋白(SF)作为一种特殊的天然聚合物,具有优异的生物相容性、生物降解性和双亲性,是制备柔性传感器的良好候选者.然而,丝素蛋白的高结晶度和结晶不可控性使获得这种出色的仿生水凝胶传感器具有挑战性.纯SF水凝胶是脆性的,没有黏性.在... 详细信息

丝素蛋白(SF)作为一种特殊的天然聚合物,具有优异的生物相容性、生物降解性和双亲性,是制备柔性传感器的良好候选者.然而,丝素蛋白的高结晶度和结晶不可控性使获得这种出色的仿生水凝胶传感器具有挑战性.纯SF水凝胶是脆性的,没有黏性.在此,我们通过引入聚丙烯酰胺(PAM)到SF水凝胶中来解决这一问题.由于SF/PAM水凝胶具有较强的分子间相互作用,其网络形貌由欧几里得孔改变为非欧几里得孔.同时,其β片结晶很容易被抑制到纳米尺度.这些演变不仅使SF/PAM水凝胶具有优异的机械性能,而且具有出色的黏附性能.与纯PAM水凝胶相比,SF8/PAM水凝胶的拉伸强度、拉伸破坏应变、抗压强度(80%应变下)和黏附性能(在猪皮上)分别提高了133.1%、120.9%、610.8%和104.8%.此外,SF的双亲性可以使碳纳米管(CNTs)在水凝胶中分散良好.制备的CNT0.3/SF8/PAM水凝胶继承并进一步改善了上述性能.除此之外,它还表现出优异的自黏附传感性能,最大灵敏度因子高达10.13,工作应变范围超过1000%,大应变下稳定循环拉伸达500次以上.同时,六种人类活动的精确检测也得到了验证.本工作为实现高性能SF基水凝胶提供了新策略,并证实SF/PAM水凝胶在柔性可穿戴应变传感器中具有广阔的应用前景.

关键词： silk fibroin intermolecular interaction network morphology β-crystallization adhesion hydrogel strain sensor

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Slow Photon-Enhanced Heterojunction Accelerates Photocatalytic Hydrogen Evolution Reaction to Unprecedented Rates

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CCS Chemistry 2023年第2期5卷 372-384页

作者： Jing Liu Yin-Hao Guo Zhi-Yi Hu Heng Zhao Ze-Chuan Yu Lihua Chen Yu Li Gustaaf Van Tendeloo Bao-Lian Su State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology430070 Wuhan Nanostructure Research Centre(NRC) Wuhan University of Technology430070 Wuhan School of Civil Engineering and Architecture Wuhan University of Technology430070 Wuhan EMAT University of AntwerpB-2020 Antwerp Laboratory of Inorganic Materials Chemistry(CMI) University of NamurB-5000 Namur

In photocatalysis,both the photogenerated charge separation and transport and the induced light utilization greatly influence *** this work,highly ordered CdS@ZnO core-shell inverse opal(CdS@ZnO-csIO)nanocomposites have been successfully designed as a model to couple the heterojunction system with the slow photon effect for photocatalytic H2 *** calculations and experimentation provide direct evidence for the slow photon effect in the CdS@ZnO-csIO *** type II heterojunction is responsible for promoting the migration and separation of photogenerated charges,and the slow photon effect is in charge of enhancing light harvesting in the CdS@ZnO-csIO *** synergy of two functions gives rise to a significantly enhanced photocatalytic H2 production rate under simulated solar light for the CdS@ZnO-csIO *** highest H2 production rate reaches 48.7 mmol g^(−1)h^(−1)under simulated solar light with the benchmark performance for all reported CdS@ZnO *** work provides proof-of-principle that coupling the heterojunction system with the slow photon effect can greatly enhance the photocatalytic activity of composite photocatalysts.

关键词： type II heterojunction slow photon effect CdS@ZnO nanocomposites 3D core-shell inverse opal nanocomposites photocatalytic H2 production

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Boosting molecular diffusion following the generalized Murray's Law by constructing hierarchical zeolites for maximized catalytic activity

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国家科学评论（英文版） 2022年第12期9卷 143-156页

作者： Ming-Hui Sun Shu-Shu Gao Zhi-Yi Hu Tarek Barakat Zhan Liu Shen Yu Jia-Min Lyu Yu Li Shu-Tao Xu Li-Hua Chen Bao-Lian Su State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium Division of Analysis Sinopec Beijing Research Institute of Chemical IndustryBeijing 100013China National Engineering Laboratory for Methanol to Olefins Dalian National Laboratory for Clean EnergyDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Nanostructure Research Centre Wuhan University of TechnologyWuhan 430070China Laboratory of Inorganic Materials Chemistry(CMI) University of NamurNamur B-5000Belgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China National Engineering Laboratory for Methanol to Olefins Dalian National Laboratory for Clean EnergyDalian Institute of Chemical PhysicsChinese Academy of SciencesDalian 116023China

Diffusion is an extremely critical step in zeolite catalysis that determines the catalytic performance,in particular for the conversion of bulky *** interconnected mesopores and macropores into a single microporous zeolite with the rationalized pore size at each level is an effective strategy to suppress the diffusion limitations,but remains highly challenging due to the lack of rational design ***,we demonstrate the first example of boosting molecular diffusion by constructing hierarchical Murray zeolites with a highly ordered and fully interconnected macro-meso-microporous structure on the basis of the generalized Murray's *** a hierarchical Murray zeolite with a refined quantitative relationship between the pore size at each length scale exhibited 9 and 5 times higher effective diffusion rates,leading to 2.5 and 1.5 times higher catalytic performance in the bulky 1,3,5-triisopropylbenzene cracking reaction than those of microporous ZSM-5 and ZSM-5 nanocrystals,*** concept of hierarchical Murray zeolites with optimized structural features and their design principles could be applied to other catalytic reactions for maximized performance.

关键词： catalytic cracking generalized Murray's Law hierarchical Murray structure ordered porous hierarchy zeolites

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Interdisciplinary exploration between magnetism and thermoelectricity

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Science Bulletin 2022年第9期67卷 891-894,M0003页

作者： Cuncheng Li Wenyu Zhao Qingjie Zhang State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Thermoelectrics have important applications in power generation and refrigeration through the direct energy conversion between heat and *** performance of thermoelectric(TE)materials can be qualified by dimensionless figure of merit ZT=σa2/κ,whereσ,a andκare the electrical conductivity,Seebeck coefficient and thermal conductivity,respectively.

关键词： conductivity Seebeck electrical

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Tunable Atomic-Scale Steps and Cavities Break Both Stability and Activity Limits of CoO_(x) Nanosheets to Catalyze Oxygen Evolution

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Renewables 2023年第4期1卷 465-473页

作者： Min Yu Xueqin Mu Weitao Meng Ziyue Chen Yu Tong Yu Ge Shiyuan Pang Shengjie Li Suli Liu Shichun Mu Key Laboratory of Advanced Functional Materials of Nanjing Nanjing Xiaozhuang UniversityNanjing 211171 State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070

A highly active interface can enhance the catalytic efficiency of catalysts toward the oxygen evolution reaction(OER).However,accurately tuning their atomic interface configurations of defects with sufficient activity and stability remains a grand ***,we report on breaking the activity and stability limits of CoO_(x) nanosheets in the OER process by constructing copious high-energy atomic steps and cavities,in which S or Ce atoms simultaneously replace O or Co atoms from CoO_(x),thus achieving high-energy atomic interface Ce,O-Co_(3)S_(4) *** combining in situ characterization and density functional theory calculations,it is shown that the unique orbital coupling between Ce-4f,O(S)-2p,and Co-3d causes it to be closer to the Fermi level,leading to faster charge transfer *** importantly,the novel structure breaks the stability limit of cobalt sulfide with planar defects,which gives high catalytic activity and stability in 0.1 M KOH solutions,better than commercial RuO_(2) and IrO_(2) noble metal *** expected,Ce,O-Co_(3)S_(4) possesses much better turnover frequency activity(0.064 s^(-1))at an overpotential of 300 mV,which is ~7 times larger than that of Ce-CoO_(x)(0.009 s^(-1)).Our work presents a new perspective of designing catalysts with atomically dispersed orbital electronic coupling defects toward efficient OER electrocatalysis.

关键词： atomic replacement amorphous structures interface active centers atomic defect oxygen evolution reaction

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Aqueous batteries:from laboratory to market

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国家科学评论（英文版） 2023年第11期10卷 85-88页

作者： Xikun Zhang Pengcheng Xing Thomas L.Madanu Jing Li Jie Shu Bao-Lian Su Laboratory of Inorganic Materials Chemistry(CMI) University of NamurBelgium School of Materials Science and Chemical Engineering Ningbo UniversityChina Laboratory of Inorganic Materials Chemistry(CMI) University of NamurBelgium State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyChina

As estimated up to 2022,global installed capacity of lithium-ion batteries(LIBs)has increased dramatically from 148 to 580 GWh in the past five *** wide range of applications is mainly at-tributed to their high energy density,ex-cellent cycle life,and low self-discharge rate[1].However,with the continuous promotion of the applications in various fields,the limitations of LIBs have be-come apparent,such as high cost and safety issues.

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BaTiO_(3)/Polyurethane Dielectric Composites with Diels-Alder Bond for Improved Self-Healing Properties

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Journal of Renewable materials 2022年第9期10卷 2355-2364页

作者： unlong Yao Wei Nie Zhengguang Sun Huan Yang Yu Guan Lin Gao Xueliang Jiang Mujie Guo Chuanxi Xiong Hubei Key Laboratory of Plasma Chemistry and Advanced Materials School of Materials Science and EngineeringWuhan Institute of TechnologyWuhan430205China Ministry-of-Education Key Laboratory for the Green Preparation and Application of Functional Materials Hubei UniversityWuhan430062China Key Laboratory of Green Chemical Engineering Process of Ministry of Education Wuhan Institute of TechnologyWuhan430205China School of Chemistry and Environmental Engineering Jianghan UniversityWuhan430056China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and School of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China

In general,self-healing dielectric composites are mainly composed of polar hydrogen bonds,which have high hydrophilicity and are unsuitable for humid *** composite with Diels-Alder(D-A)bond contains covalent bonds,it can be adopted as an efficient self-healing ***,we construct self-healing barium titanate(BT)/polyurethane(PU)dielectric composites by adopting PU with D-A bond as matrix(BT/PU-DA).The prepared 10%BT/PU-DA composite exhibits superior self-healing ability than that of ***,its dielectric constant can reach 9.3 with a loss of only 0.04 at 1000 Hz and maintain 93%repair efficiency of tensile *** experimental analysis suggests the introduction of D-A bond can enhance the thermostability and self-healing ability of BT/PU-DA *** addition,the incorporation of BT nanoparticles and D-A bond in the self-healing composite contributes to the lower dielectric loss and excellent tensile strength after *** adopted strategy is a promising and facile approach to develop highly efficient selfhealing dielectric material,which will be conducive to reuse and sustainable development of the electronic packaging material in aqueous medium or wet environment.

关键词： Diels-Alder bond self-healing dielectric properties tensile strength polyurethane

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synthesis of highly sinterable MgO powders for IR transparent ceramics

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Ceramics International 2025年

作者： Zhi, Yongli Mei, Bingchu Li, Weiwei Cheng, Jing Luo, Peng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan430070 China Jianghuai Advance Technology Center Hefei230000 China

MgO transparent ceramics (TCS) have attracted great interests in the field of infrared window materials due to its wide transmission range, excellent thermal conductivity, and balanced mechanical properties. To date, research on MgO transparent ceramics predominantly relies on commercial MgO powders by spark plasma sintering (SPS). Herein, we report highly sinterable MgO powders synthesized by co-precipitation method, which exhibits pure phase and particle size of 75 nm. When sintered at 950 °C under 45 MPa for 2 h by hot pressed (HP) method, the transmittance of the MgO ceramic sample with the thickness of 2 mm achieved 76.9 % at 0.4 μm and 88.3 % at 5 μm. These optical properties are comparable to or even superior to MgO TCS produced through SPS method. This work shows that the MgO particles synthesized via the co-precipitation method are suitable for producing high optical quality of MgO infrared (IR) transparent ceramics. © 2025

关键词： Thermal conductivity

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