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

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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Triphenylphosphine oxide additive regulates the growth of perovskite films by evaporation-spraying technique for high-efficiency large-area solar cell modules

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Journal of Energy Chemistry 2025年 108卷 468-476页

作者： Zhu, Mingwei Ruan, Danlin Zhao, Xin Song, Jiawei Cheng, Jiahao Shen, Wenjian Li, Wangnan Liang, Guijie Liang, Ying Peng, Yong Li, Bin Cheng, Yi-Bing Hubei Xiangyang441000 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Hubei Wuhan430070 China Machine X Technology Co. Ltd. Zhejiang Jiaxing314211 China Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices Hubei University of Arts and Science Hubei Xiangyang441053 China State Key Laboratory of Advanced Processing and Recycling of Non-Ferrous Metals Lanzhou University of Technology Gansu Lanzhou730050 China

Premature perovskite films rapidly form at the FAI/PbI2 interface, inhibiting further reactions between FAI and PbI2 during the fabrication of perovskite films via the evaporating-spraying hybrid method according to our previous research. In this research, triphenylphosphine oxide (TPPO) was proved to be an effective coordinator that reduces the reaction rate between FAI and PbI2 at the initial stage, which can be attributed to the hydrogen (H) bonds between FA+ and TPPO, and coordinate bonds between TPPO and PbI2. Additionally, the quality of perovskite films improved significantly: the trap state density decreased from 1.6 × 1018 to 3.17 × 1017 cm−3, while the crystal size increased from 740 to 940 nm. The champion perovskite device achieved a remarkable efficiency of 20.93% (0.09 cm2) and 16.75% (63.7 cm2), marking one of the highest reported results for the evaporating-spraying hybrid method. Moreover, the perovskite solar cells retained over 80% of their initial performances after 600 h of storage at 60 °C in a nitrogen environment without encapsulation. It also maintained approximately 90% of its initial performance after continuous illumination at 25 °C for 1400 h under the same conditions. © 2025 Science Press

关键词： Crystal growth from melt

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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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Vacancy-Based Defect Regulation for High Thermoelectric Performance in Ge9Sb2Te12-x Compounds

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ACS APPLIED materials & INTERFACES 2020年第17期12卷 19664-19673页

作者： Chen, Shuo Bai, Hui Li, Junjie Pan, Wenfeng Jiang, Xianyan Li, Zhi Chen, Zhiquan Yan, Yonggao Su, Xianli Wu, Jinsong Uher, Ctirad Tang, Xinfeng State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Hubei Nuclear Solid Physics Key Laboratory Department of Physics Wuhan University Wuhan 430072 China Hubei Nuclear Solid Physics Key Laboratory Department of Physics Wuhan University Wuhan 430072 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Hubei Nuclear Solid Physics Key Laboratory Department of Physics Wuhan University Wuhan 430072 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China Department of Physics University of Michigan Ann Arbor Michigan 48109 United States State Key Laboratory of Advanced Technology for Materials Synthesis and Processing Wuhan University of Technology Wuhan 430070 China

Defect engineering is the core strategy for improving thermoelectric properties. Herein, cation doping along with modulation of cation vacancy has been developed in GeTe-based materials as an effective method to induce vacancy-based defects to boost their thermoelectric performance. A series of ternary compounds of Ge9Sb2Te12-x (x = 0, 0.03, 0.06, 0.09, 0.12, 0.15) was prepared by vacuum-melting and annealing combined with the spark plasma sintering (SPS) process. The role of Sb doping and cation vacancy on thermoelectric properties was systematically investigated. It is found that alloying Sb2Te3 into GeTe increases the concentration of cation vacancies, which is corroborated by both positron annihilation measurements and theoretical calculations. The vacancies, stacking faults, and planar defect interactions determine the thermoelectric transport properties. Adjusting the deficiency of Te effectively tunes the concentration of cation vacancies and dopant defects in the structure. In turn, this tunes the carrier concentration close to its optimum. A high power factor of 32.6 mu W cm(-1) K-2 is realized for Ge9Sb2Te11.91 at 725 K. Moreover, large strains induced by the defect structures, including Sb dopant, vacancy, staking faults, as well as planar defects intensify phonon scattering, leading to a significant decrease in the thermal conductivity from 7.6 W m(-1) K-1 for pristine GeTe to Ge9Sb2Te11.85 at room temperature. All of the above contribute to a high ZT value of 2.1 achieved for the Ge9Sb2Te11.91 sample at 775 K.

关键词： GeTe-based compounds alloying with Sb2Te3 deficiency of Te stacking fault vacancy plane thermoelectric

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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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Multi-functionalized sites in metalated COFs film for chemiresistive gas sensing at room temperature

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Chemical Engineering Journal 2025年 514卷

作者： Mei, Aohan Zhou, Min Zhang, Wenyuan Bao, Yunan Liu, Yueli Chen, Wen State Key Laboratory of Silicate Materials for Architectures School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China State Key Laboratory of Advanced Technology for Materials Synthesis and Processing School of Materials Science and Engineering Wuhan University of Technology Wuhan430070 China Wuhan Brilliant Tech Co. Ltd. Wuhan430205 China

Post-synthetic modification of covalent organic frameworks (COFs) has attracted much attention due to its simple introduction of metals and functional groups as active sites for diverse applications. However, the charge transport improvement and the functions of active sites in metalated COFs are so far ignored in gas sensors. Herein, Zn2+ is loaded on two kinds of sites on TpBpy COFs film by a simple photochemical synthesis. Zn2+ coordination improves the NH3 sensitivity by increasing the charge density and adsorption of ammonia molecules. DFT simulation and UPS result prove that the suitable adsorption configuration and work function of Zn@TpBpy COFs film play the key role for the gas sensing behavior. The as-fabricated Zn@TpBpy COFs gas sensors exhibit high sensitivity with linear response behavior and a low detection limit of 500 ppb. By comparing Zn@TpBpy with Cu@TpBpy COFs, the electron donating coordination structure from the fully occupied 3d orbital in Zn2+ boosts the response value and sensing speed, providing a novel insight into manipulating sensing behavior of metalated COFs films. © 2025 Elsevier B.V.

关键词： Chemical sensors

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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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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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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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