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Strategic modulation of CoFe sites for advanced bifunctional oxygen electrocatalyst

Chinese Journal of Structural Chemistry 2025年第1期44卷 57-62页

作者： Juhong Zhou Hui Zhao Ping Han Ziyue Wang Yan Zhang Xiaoxia Mao Konglin Wu Shengjue Deng Wenxiang He Binbin Jiang Anhui Provincial Key Laboratory of Advanced Catalysis and Energy Materials School of Chemistry and Chemical EngineeringAnqing Normal UniversityAnqing246001China State Key Laboratory of Heavy Oil Processing China University of Petroleum(East China)Qingdao266580China Guangdong Wentai New Energy Co. LtdGuangdong528300China Engineering Research Center of Biofilm Water Purification and Utilization Technology of Ministry of Education Anhui University of TechnologyMaanshan243032China State Key Laboratory of Marine Resource Utilization in South China Sea Department of Materials Science and EngineeringHainan UniversityHaikou570228China

An effective strategy of regulating active sites in bifunctional oxygen electrocatalysts is essentially desired,especially in rechargeable metal-air batteries(RZABs).Herein,a highly efficient electrocatalyst of CoFe alloys embedded in pyridinic nitrogen enriched N-doped carbon(CoFe/P-NC)is intelligently constructed by pyrolysis *** high concentration of pyridinic nitrogen in CoFe/P-NC can significantly reprogram the redistribution of electron density of metal active sites,consequently optimizing the oxygen adsorption *** expected,the pyridinic nitrogen guarantees CoFe/P-NC providing the low overpotential of the overall oxygen electrocatalytic process(ΔEORR-OER=0.73 V ***)and suppresses the benchmark electrocatalysts(Pt/C&RuO_(2)).Assembled rechargeable Zn-air battery using CoFe/P-NC demonstrates a promising peak power density of 172.0 mW cm^(-2),a high specific capacity of 805.0 mAh g^(-1)Zn and an excellent *** work proposes an interesting strategy for the design of robust oxygen electrocatalysts for energy conversion and storage fields.

关键词： Bifunctional oxygen electrocatalyst Bimetallic alloys Pyridinic nitrogen Zn-air battery

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Phosphorus-doped NiS_(2)electrocatalyst with a hybrid structure for hydrogen evolution

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Science China(Technological Sciences) 2022年第7期65卷 1506-1512页

作者： ZHOU Qi LIU HaoRui JIAO SunZhi FENG ChenChen State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals Lanzhou University of TechnologyLanzhou 730050China School of Materials Science and Engineering Lanzhou University of TechnologyLanzhou 730050China College of Mechanical Engineering Longdong UniversityQingyang 745000China

In this article,P-NiS_(2)/Ni_(x)P electrocatalysts were synthesized by dealloying the Ni-Al precursor followed by phosphosulfide *** found that the hybrid structure of P-NiS_(2)/Ni_(x)P provides rich active sites for the surface hydrogen evolution reaction (HER),and the doping of P enhances the electronic conductivity of *** particular,the obtained electrode shows a low overpotential of 196 mV at 10 mA cm^(-2)and a small Tafel slope of only 110 mV dec^(-1)in the ***,longterm constant current electrolysis test experiments indicate that P-NiS_(2)/Ni_(x)P has good service *** research will help to open a new window on the design and fabrication of HER electrocatalysts.

关键词： nickle phosphosulfides hybrid structure hydrogen evolution reaction dealloying

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Ultralow Interfacial Thermal Resistance of Graphene Thermal Interface materials with Surface Metal Liquefaction

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Nano-Micro Letters 2023年第1期15卷 183-196页

作者： Wen Dai Xing-Jie Ren Qingwei Yan Shengding Wang Mingyang Yang Le Lv Junfeng Ying Lu Chen Peidi Tao Liwen Sun Chen Xue Jinhong Yu Chengyi Song Kazuhito Nishimura Nan Jiang Cheng-Te Lin Key Laboratory of Marine Materials and Related Technologies Zhejiang Key Laboratory of Marine Materials and Protective TechnologiesNingbo Institute of Materials Technology and Engineering(NIMTE)Chinese Academy of SciencesNingbo 315201People’s Republic of China Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of SciencesBeijing 100049People’s Republic of China Institute of Advanced Technology Shandong UniversityJinan 250100People’s Republic of China Ningbo Institute of Materials Technology and Engineering(NIMTE) Chinese Academy of SciencesNingbo 315201People’s Republic of China The State Key Laboratory of Metal Matrix Composites School of Materials Science and EngineeringShanghai Jiao Tong University800 Dong Chuan RoadShanghai 200240People’s Republic of China Advanced Nano-Processing Engineering Lab Mechanical Systems EngineeringKogakuin UniversityTokyo 192-0015Japan

Developing advanced thermal interface materials(TIMs)to bridge heat-generating chip and heat sink for constructing an efficient heat transfer interface is the key technology to solve the thermal management issue of high-power semiconductor *** on the ultra-high basal-plane thermal conductivity,graphene is an ideal candidate for preparing high-performance TIMs,preferably to form a vertically aligned structure so that the basal-plane of graphene is consistent with the heat transfer direction of ***,the actual interfacial heat transfer efficiency of currently reported vertically aligned graphene TIMs is far from *** addition to the fact that the thermal conductivity of the vertically aligned TIMs can be further improved,another critical factor is the limited actual contact area leading to relatively high contact thermal resistance(20-30 K mm^(2) W^(−1))of the“solid-solid”mating interface formed by the vertical graphene and the rough chip/heat *** solve this common problem faced by vertically aligned graphene,in this work,we combined mechanical orientation and surface modification strategy to construct a three-tiered TIM composed of mainly vertically aligned graphene in the middle and micrometer-thick liquid metal as a cap layer on upper and lower *** on rational graphene orientation regulation in the middle tier,the resultant graphene-based TIM exhibited an ultra-high thermal conductivity of 176 W m^(−1) K^(−1).Additionally,we demonstrated that the liquid metal cap layer in contact with the chip/heat sink forms a“liquid-solid”mating interface,significantly increasing the effective heat transfer area and giving a low contact thermal con-ductivity of 4-6 K mm^(2) W^(−1) under packaging *** finding provides valuable guidance for the design of high-performance TIMs based on two-dimensional materials and improves the possibility of their practical application in electronic thermal management.

关键词： Vertically aligned graphene Liquid metal Surface modification Thermal interface materials

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Boosting Peroxymonosulfate Activation via Co-Based LDH-Derived Magnetic Catalysts:A Dynamic and Static state Assessment of Efficient Radical-Assisted Electron Transfer Processes

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Energy & Environmental materials 2024年第5期7卷 301-312页

作者： Wenhan Yang Junming Xia Fanfan Shang Ge Ge Yang Bin Wang Hairui Cai Lingyun Jing Hao Zhu Shengchun Yang Chao Liang Guosheng Shao MOE Key Laboratory for Nonequilibrium Synthesis and Modulation of Condensed Matter School of PhysicsNational Innovation Platform(Center)for Industry-Education Integration of Energy Storage TechnologyXi'an Jiaotong UniversityXi'an 710000China State Key Laboratory of Organic Electronics and Information Displays&Institute of Advanced Materials(1AM) Nanjing University of Posts&Telecommunications9 Wenyuan RoadNanjing 210023China College of Petroleum and Chemical Engineering Lanzhou University of TechnologyLanzhou 730050China Key Laboratory of Western China's Environmental Systems(Ministry of Education)and Gansu Engineering Research Center of Fine Particles Pollution Control Technology and Equipment College of Earth and Environmental SciencesLanzhou UniversityLanzhou 730000China State Center for International Cooperation on Designer Low-Carbon&Environmental Materials(CDLCEM) School of Materials Science and EngineeringZhengzhou UniversityZhengzhou 450001China

Heterogeneous catalysts promoting efficient production of reactive species and dynamically stabilized electron transfer mechanisms for peroxomonosulfates(PMS)still lack systematic ***,a more stable magnetic layered double oxides(CFLDO/N-C),was designed using self-polymerization and high temperature carbonization of *** CFLDO/N-C/PMS system effectively activated PMS to remove 99%(k=0.737 min^(-1))of tetracycline(TC)within 10 *** CFLDO/N-C/PMS system exhibited favorable resistance to inorganic anions and natural organics,as well as satisfactory suitability for multiple *** magnetic properties of the catalyst facilitated the separation of catalysts from the liquid phase,resulting in excellent reproducibility and effectively reducing the leaching of metal *** electronic bridge was constructed between cobalt(the active platform of the catalyst)and PMS,inducing PMS to break the O-O bond to generate the active *** combination of static analysis and dynamic evolution confirmed the effective adsorption of PMS on the catalyst surface as well as the strong radical-assisted electron transfer ***,we further identified the sites where the reactive species attacked the TC and evaluated the toxicity of the *** findings offer innovative insights into the rapid degradation of pollutants achieved by transition metals in SR-AOPs and its mechanistic elaboration.

关键词： advanced oxidation process degradation mechanisms electron transport layered double hydroxide reactive species

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High-entropy alloy nanocrystals boosting photocatalytic hydrogen evolution coupled with selective oxidation of cinnamyl alcohol

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Chinese Journal of Catalysis 2025年第1期68卷 326-335页

作者： Xianglin Xiang Bei Cheng Bicheng Zhu Chuanjia Jiang Guijie Liang Faculty of Materials Science and Engineering Kunming University of Science and TechnologyKunming 650093YunnanChina State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070HubeiChina Laboratory of Solar Fuel Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430078HubeiChina College of Environmental Science and Engineering Nankai UniversityTianjin 300350China Hubei Key Laboratory of Low Dimensional Arts and Science Hubei University of Arts and ScienceXiangyang 441053HubeiChina

Photocatalysis provides a promising solution to the worldwide shortages of energy and industrially important raw materials by utilizing sunlight for coupled hydrogen(H_(2))production with controllable organic ***,we demonstrate that PtFeNiCoCu high-entropy alloy(HEA)nanocrystals can act as efficient cocatalysts for H_(2)evolution coupled with selective oxidation of cinnamyl alcohol to cinnamaldehyde by cubic cadmium sulfide(CdS)quantum dots(QDs)with uniform sizes of 4.0±0.5 *** nanocrystals were prepared via a simple solvothermal approach,and were successfully integrated with CdS QDs by an electrostatic self-assembly method to construct HEA/CdS *** optimized HEA/CdS sample presented an enhanced photocatalytic H_(2)production rate of 7.15 mmol g^(-1)h^(-1),which was 13 times that of pure CdS ***,a cinnamyl alcohol conversion of 96.2%with cinnamaldehyde selectivity of 99.5%was achieved after photoreaction for 3 *** integration of HEA with CdS QDs extended the optical absorption edge from 475 to 484 *** d-band center analysis,Pt atoms in the HEA are the active sites for H_(2)evolution,exhibiting higher catalytic activity than pure ***,the band structure of the CdS QDs enables the oxidative transformation of cinnamyl alcohol to cinnamaldehyde with high ***,femtosecond transient absorption spectroscopy shows that HEA can significantly promote the separation of photogenerated carriers in CdS,which is vital for achieving enhanced photocatalytic *** work inspires atomic-level design of photocatalytic materials for coordinated production of green energy carriers and value-added products.

关键词： Artificial photosynthesis d-Band center Photocatalytic hydrogen evolution Quantum dots Value-added organic synthesis

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Fabrication and Property of SiC Ceramic with Large Thickness/Diameter Ratios

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Journal of Wuhan University of technology(materials Science) 2020年第3期35卷 506-513页

作者： TAN Lin HE Qianglong HU Lanxin TIAN Tian WANG Weimin State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China

Silicon carbide ceramics with different thicknesses/diameter ratios were prepared by using ultra-fine silicon carbide powder with the sintering additives of 1.0 wt% boron and 1.5 wt% carbon. The influence of thickness/diameter ratio on the microstructure and density of SiC ceramics was investigated in detail. The experimental results show that the addition of boron and carbon sintering aids can promote the densification process of SiC ceramic, leading to the low sintering temperature and improve mechanical properties. At 1950 ℃, SiC ceramic with a density of 99% exhibits Young's modulus, hardness, and flexural strength of 476 MPa, 28.3 GPa, and 334 MPa, respectively. It is found that long holding time has a positive effect on the uniformity of the microstructure and density distribution of SiC ceramics with large thickness/diameter ratios. Additionally, the sintering additive of boron can solid-solve into SiC, and then facilitate the phase transformation of SiC to form 6H-SiC and 4H-SiC composite ceramics.

关键词： SiC large thickness/diameter ratios mechanical properties uniformity

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A new strategy to access Co/N co-doped carbon nanotubes as oxygen reduction reaction catalysts

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Chinese Chemical Letters 2021年第1期32卷 535-538页

作者： Bingshuai Liu Huang Zhou Huihui Jin Jiawei Zhu Zhe Wang Chenxi Hu Lvhan Liang Shichun Mu Daping He State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of TechnologyWuhan 430070China Hubei Engineering Research Center of RF-Microwave Technology and Application Wuhan University of TechnologyWuhan 430070China

Carbon nanotubes(CNTs),as one-dimensional nanomaterials,show great potential in energy conversion and storage due to their efficient electrical conductivity and mass ***,the security risks,time-consuming and high cost of the preparation process hinder its further ***,we develop that a negative pressure rather than a following gas environment can promote the generation of cobalt and nitrogen co-doped CNTs(Co/N-CNTs) by using cobalt zeolitic imidazolate framework(ZIF-67) as a precursor,in which the negative pressure plays a key role in adjusting the size of cobalt nanoparticles and stimulating the rearragement of carbon atoms for forming ***,the obtained Co/N-CNTs,with high content of pyridinic nitrogen and abundant graphitized structure,exhibit superior catalytic activity for oxygen reduction reaction(ORR) with half-wave potential(E_(1/2)) of 0.85 V and durability in terms of the minimum current loss(2%) after the 30,000 s *** development provides a new pathway for large-scale and cost-effective preparation of metal-doped CNTs for various applications.

关键词： Negative pressure Cobalt zeolitic imidazolate framework Cobalt and nitrogen co-doped Carbon nanotubes Oxygen reduction reaction

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Fabrication and Characterization of Pressure Sensors Based on Xanthan Gum and Pullulan 16

Fabrication and Characterization of Pressure Sensors Based o...

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16th Textile Bioengineering and Informatics Symposium, TBIS 2023

作者： Zhang, Ya-Qi Liu, Shi-Yao Tao, Yong-Zhen State Key Laboratory for Textile Materials and Advanced Processing Technology Wuhan Textile University Wuhan China College of Material Science and Engineering Wuhan Textile University Wuhan China

ISBN: (纸本)9781713879473

Conductive hydrogels based on biopolymers have potential applications in the field of wearable devices, implantable devices, and human-machine interfaces due to their biocompatibility as well as conductivity. However, hydrogels are prone to water loss under dry atmospheres. In this paper, a biopolymer-based pressure sensor with water retention was designed. Xanthan gum (XG) and pullulan (P) were cross-linked with sodium trimetaphosphate (STMP) to prepare XG5-P-STMP, and polyethylene glycol with a molecular weight of 200 (PEG200) was added into hydrogels to improve moisture retention. The mechanical properties of the hydrogels were investigated by rheologic measurements such as time sweep, frequency sweep, and strain sweep. The results showed that the addition of PEG200 enhanced strength and moisture retention of the hydrogels, and high PEG200 content hindered the recovery property of the hydrogels. Furthermore, the XG5-P-PEG-STMP hydrogel with ionic conductivity and recoverability was explored as a pressure sensor, and the resistance change ratio exhibited repeatable profile. This work provides some valuable information for further applications of natural polysaccharides as intelligent flexible elections. © TBIS 2023. All rights reserved.

关键词： Hydrogels

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Structure stability, electronic property and voltage profile of LiFe_(1-n)NnP_(1-m)M_(m)O_(4) olivine cathode material

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Rare Metals 2021年第12期40卷 3512-3519页

作者： Zhi-Hong Cui Xue-Feng Lu Jian-Hua Luo Xin Guo Hong-Tao Xue Fu-Ling Tang State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metal Department of Materials Science and EngineeringLanzhou University of TechnologyLanzhou 730050China

First-principles computational studies under density functional theory(DFT) framework were used to investigate the structural stability, conductivity and voltage profile of LiFe_(1-n)NnP_(1-m)M_(m)O_(4)(N, M = Si or S) electrode materials. It is found that the Li FeP_(7/8)Si_(1/8)O_(4) system has the most stable structure. After doping, the band gap values of the systems decrease gradually, and LiFe_(7/8)S_(1/8)PO_(4) system has a minimum band gap of 1.553 e V, attributed to the hybridization of the Fe-d and S-p orbital electrons. The Li Fe P7/8 S1/8 O4 system demonstrates the characteristic of n-type semiconductor, and other doping systems have the feature of p-type semiconductor. Charge density difference maps show that the covalent property of Si-O bond is enhanced in the Li FeP_(7/8)Si_(1/8)O_(4) system. The average distance of Li and O atoms in the S doping systems increases from 0.21026 to 0.21486 and 0.21129 nm, respectively,indicating that doping broadens significantly the channel of Li ion de-intercalation in LiFe_(7/8)S_(1/8)PO_(4) and LiFeP_(7/8)S_(1/8)O_(4). Additionally, the results of lithium intercalation potential imply that the voltages of the doping systems fallinto the range of 2.23-2.86 V.

关键词： Energy storage materials First principles Battery cathode LiFePO_(4) Doping Electronic properties

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Structure and enhanced dielectric temperature stability of BaTiO3- based ceramics by Ca ion B site-doping

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Journal of Materiomics 2021年第2期7卷 295-301页

作者： Xuewen Jiang Hua Hao Yang Yang Enhao Zhou Shujun Zhang Ping Wei Minghe Cao Zhonghua Yao Hanxing Liu Foshan Xianhu Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory Xianhu Hydrogen ValleyFoshan528200China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and EngineeringWuhan University of TechnologyWuhan430070China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing International School of Material Science and EngineeringWuhan University of TechnologyWuhan430070China Institute for Superconducting and Electronic Materials Australian Institute of Innovative MaterialsUniversity of WollongongWollongongNSW2500Australia Nanostructure Research Centre Wuhan University of TechnologyWuhan430070China

Capacitor is an important part of many electronic devices,so the temperature stability as one key parameter of capacitor needs to be improved constantly for meeting the requirements of various application ***,combined with the X-ray diffraction(XRD),selected area electron diffraction(SAED)and Vienna Ab-initio Simulation Package(VASP)calculation,it was confirmed that Ca ion can substitute the Ti site in the BaTi1-xCaxO3-x[BTC100](0≤x≤0.05)ceramics synthesized by solid-phase method which greatly improved the low-temperature stability of dielectric ***,introducing Bi3þand Zn^(2+) into BTC4 to form(1-y)BaTi0.6Ca0.04O2.96-yBi(Zn_(0.5)Ti_(0.5))O_(3)[(1-y)BTC4-yBZT](0.1≤y≤0.2)ceramics can further improve the dielectric-temperature stability by means of diffused phase transition and core-shell *** importantly,the 0.85BTC4-0.15BZT ceramics with a pseudocubic perovskite structure possessed a temperature coefficient of capacitance at 25℃(TCC25℃)being less than±15%over a wide temperature range of 55℃-200℃and a temperate dielectric constant(ε=1060)and low dielectric loss(tanδ=1.5%),which measure up to the higher standard in the current capacitor industry such as X9R requirements.

关键词： BaTiO3 Ca substituted X9R capacitors Dielectric properties

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