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Polymeric viologen-based electron transfer mediator for improving the photoelectrochemical water splitting on Sb_(2)Se_(3) photocathode

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Fundamental Research 2024年第2期4卷 291-299页

作者： Chang Liu Fusheng Li Linqin Wang Zeju Li Yilong Zhao Yingzheng Li Wenlong Li Ziqi Zhao Ke Fan Fei Li Licheng Sun State Key Laboratory of Fine Chemicals Institute of Artificial PhotosynthesisDUT-KTH Joint Education and Research Centre on Molecular DevicesInstitute for Energy Science and TechnologyDalian University of TechnologyDalian 116024China Center of Artificial Photosynthesis for Solar Fuels School of ScienceWestlake UniversityHangzhou 310024China Department of Chemistry School of Engineering Sciences in ChemistryBiotechnology and HealthKTH Royal Institute of TechnologyStockholm 10044Sweden

The photogenerated charge carrier separation and transportation of inside photocathodes can greatly influence the performance of photoelectrochemical(PEC)H2 production *** TiO_(2) with p-type semiconductors to construct heterojunction structures is one of the most widely used strategies to facilitate charge separation and ***,the band position of TiO_(2) could not perfectly match with all p-type ***,taking antimony selenide(Sb_(2)Se_(3))as an example,a rational strategy was developed by introducing a viologen electron transfer mediator(ETM)containing polymeric film(poly-1,1′-dially-[4,4′-bipyridine]-1,1′-diium,denoted as PV^(2+))at the interface between Sb_(2)Se_(3) and TiO_(2) to regulate the energy band alignment,which could inhibit the recombination of photogenerated charge carriers of *** Pt as a catalyst,the constructed Sb_(2)Se_(3)/PV^(2+)/TiO_(2)/Pt photocathode showed a superior PEC hydrogen generation activity with a photocurrent density of−18.6 mA cm^(-2) vs.a reversible hydrogen electrode(RHE)and a half-cell solar-to-hydrogen efficiency(HC-STH)of 1.54%at 0.17 V ***,which was much better than that of the related Sb_(2)Se_(3)/TiO_(2)/Pt photocathode without PV^(2+)(−9.8 mA cm^(-2),0.51%at 0.10 V ***).

关键词： Viologen Electron transfer mediator Sb2Se3 photocathode Solar water splitting Hydrogen evolution reaction

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Wear-resistant CoCrNi multi-principal element alloy at cryogenic temperature

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science Bulletin 2024年第2期69卷 227-236页

作者： Yue Ren Qing Zhou Dongpeng Hua Zhuobin Huang Yulong Li Qian Jia Peter Gumbsch Christian Greiner Haifeng Wang Weimin Liu State Key Laboratory of Solidification Processing Center of Advanced Lubrication and Seal MaterialsNorthwestern Polytechnical UniversityXi’an 710072China Institute for Applied Materials Karlsruhe Institute of TechnologyKarlsruhe 76131Germany IAM-ZM MicroTribology CenterμTC Karlsruhe Institute of TechnologyKarlsruhe 76131Germany Fraunhofer IWM Freiburg 79108Germany State Key Laboratory of Solid Lubrication Lanzhou Institute of Chemical PhysicsChinese Academy of SciencesLanzhou 730000China

Traditional high strength engineering alloys suffer from serious surface brittleness and inferior wear performance when servicing under sliding contact at cryogenic ***,we report that the recently emerging CoCrNi multi-principal element alloy defies this trend and presents dramatically enhanced wear resistance when temperature decreases from 273 to 153 K,surpassing those of cryogenic austenitic *** temperature-dependent structure characteristics and deformation mechanisms influencing the cryogenic wear resistance of CoCrNi are clarified through microscopic observation and atomistic *** is found that sliding-induced subsurface structures show distinct scenarios at different deformation *** cryogenic condition,significant grain refinement and a deep plastic zone give rise to an extended microstructural gradient below the surface,which can accommodate massive sliding deformation,in direct contrast to the strain localization and delamination at 273 ***,the temperature-dependent cryogenic deformation mechanisms(stacking fault networks and phase transformation)also provide additional strengthening and toughening of the subsurface *** features make the CoCrNi alloy particularly wear resistant at cryogenic conditions and an excellent candidate for safety–critical applications.

关键词： Multi-principal element alloy Cryogenic temperature Wear CoCrNi

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Roadmap for rechargeable batteries:present and beyond

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science China Chemistry 2024年第1期67卷 13-42页

作者： Sen Xin Xu Zhang Lin Wang Haijun Yu Xin Chang Yu-Ming Zhao Qinghai Meng Pan Xu Chen-Zi Zhao Jiahang Chen Huichao Lu Xirui Kong Jiulin Wang Kai Chen Gang Huang Xinbo Zhang Yu Su Yao Xiao Shu-Lei Chou Shilin Zhang Zaiping Guo Aobing Du Guanglei Cui Gaojing Yang Qing Zhao Liubing Dong Dong Zhou Feiyu Kang Hu Hong Chunyi Zhi Zhizhang Yuan Xianfeng Li Yifei Mo Yizhou Zhu Dongfang Yu Xincheng Lei Jianxiong Zhao Jiayi Wang Dong Su Yu-Guo Guo Qiang Zhang Jun Chen Li-Jun Wan CAS Key Laboratory of Molecular Nanostructure and Nanotechnology CAS Research/Education Center for Excellence in Molecular SciencesBeijing National Laboratory for Molecular Sciences(BNLMS)Institute of ChemistryChinese Academy of Sciences(CAS)Beijing 100190China University of Chinese Academy of sciences.Beijing 100049 China Institute of Advanced Battery Materials and Devices Faculty of Materials and ManufacturingBeijing University of TechnologyBeijing 100124China Key Laboratory of Advanced Functional Materials Ministry of EducationBeijing University of TechnologyBeijing 100124China Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology Department of Chemical EngineeringTsinghua UniversityBeijing 100084China State Key Laboratory of Chemistry and Utilization of Carbon-Based Energy Resources College of ChemistryXinjiang UniversityUrumqi 830046China Department of Chemical Engineering Shanghai Jiao Tong UniversityShanghai 200240China State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied ChemistryChangchun 130022China Institute for Carbon Neutralization College of Chemistry and Materials EngineeringWenzhou UniversityWenzhou 325035China School of Chemical Engineering and Advanced Materials The University of AdelaideAdelaide 5000Australia Qingdao Industrial Energy Storage Research Institute Qingdao Institute of Bioenergy and Bioprocess TechnologyChinese Academy of SciencesQingdao 266101China Frontiers science Center for New Organic Matter Key Laboratory of Advanced Energy Materials Chemistry(Ministry of Education)College of ChemistryNankai UniversityTianjin 300071China College of Chemistry and Materials science Jinan UniversityGuangzhou 511443China Tsinghua Shenzhen International Graduate School Tsinghua UniversityShenzhen 518055China Department of Materials science and Engineering City University of Hong KongHong Kong 999077China Division of Energy Storage Dalian National Laboratory for Clean Energy(DNL)Dalian Institute of Chem

Rechargeable batteries currently hold the largest share of the electrochemical energy storage market,and they play a major role in the sustainable energy transition and industrial decarbonization to respond to global climate *** to the increased popularity of consumer electronics and electric vehicles,lithium-ion batteries have quickly become the most successful rechargeable batteries in the past three decades,yet growing demands in diversified application scenarios call for new types of rechargeable *** efforts are made to developing the next-generation post-Li-ion rechargeable batteries,which include,but are not limited to solid-state batteries,lithium–sulfur batteries,sodium-/potassium-ion batteries,organic batteries,magnesium-/zinc-ion batteries,aqueous batteries and flow *** the great achievements,challenges persist in precise understandings about the electrochemical reaction and charge transfer process,and optimal design of key materials and interfaces in a *** roadmap tends to provide an overview about the current research progress,key challenges and future prospects of various types of rechargeable *** computational methods for materials development,and characterization techniques will also be discussed as they play an important role in battery research.

关键词： energy storage rechargeable batteries battery materials electrochemistry

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Triple the steady-state reaction rate by decorating the In_(2)O_(3)surface with SiO_(x)for CO_(2)hydrogenation

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Journal of Energy Chemistry 2024年第8期95卷 96-105,I0003页

作者： Hao Wang Chun Yang Xiaoyan Yu Mingrui Wang Runze Yang Xiaowa Nie Ben Hang Yin Alex C.K.Yip Chunshan Song Guanghui Zhang Xinwen Guo State Key Laboratory of Fine Chemicals Frontier Science Center for Smart MaterialsPSU-DUT Joint Center for Energy ResearchSchool of Chemical EngineeringDalian University of TechnologyDalian 116024LiaoningChina Department of Chemistry the Chinese University of Hong KongHong Kong 999077China Paihau-Robinson Research Institute the MacDiarmid Institute for Advanced Materials and NanotechnologyVictoria University of WellingtonWellington 6012New Zealand Department of Chemical and Process Engineering The University of CanterburyChristchurch 8041New Zealand

Indium oxide(In_(2)O_(3)),as a promising candidate for CO_(2)hydrogenation to C_(1) products,often suffers from sintering and activity decline,closely related to the undesirable structural evolution under reaction *** on the comprehension of the dynamic evolution,this study presents an efficient strategy to alleviate the agglomeration of In_(2)O_(3)nanoparticles by the surface decoration with highly dispersed silica species(SiO_(x)).Various structural characterizations combined with density functional theory calculations demonstrated that the sintering resulted from the over-reduction,while the enhanced stability originated from the anchoring effect of highly stable In-OSi bonds,which hinders the substantial formation of metallic In(In^(0))and the subsequent agglomeration.0.6Si/In_(2)O_(3)exhibited CO_(2)conversion rate of10.0 mmol g^(-1)h^(-1)at steady state vs.3.5 mmol g^(-1)h^(-1)on In_(2)O_(3)in CO_(2)*** steady-state activity was also achieved on Pd-modified *** to the traditional Pd/In_(2)O_(3)catalyst,the methanol production rate of Pd catalyst supported on 0.6Si/In_(2)O_(3)was enhanced by 23%,showing the potential of In_(2)O_(3)modified by SiO_(x)in serving as a platform *** work provides a promising method to design new In_(2)O_(3)-based catalysts with improved activity and stability in CO_(2)hydrogenation.

关键词： CO_(2)hydrogenation In_(2)O_(3)sintering Dynamic structural evolution Surface SiO_(x)modification DFT simulations

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The ionic parachor and predicting properties of amino acid ionic liquid homologues of 1-alkyl-3-methylimidazolium glycine

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science China Chemistry 2012年第7期55卷 1330-1337页

作者： TONG Jing HONG Mei WANG PanPan GUAN Wei FANG DaWei YANG JiaZhen Key Laboratory qf Green Synthesis and Preparative Chemistry of Advanced Materials Liaoning UniversityShenyang 110036China

The amino acid ionic liquids （AAILs） [C3mim][Gly] （1-propyl-3-methylimidazolium glycine） and [C4mim][Gly] （l-butyl-3- methylimidazolium glycine） have been prepared by the neutralization method and characterized by IH NMR spectroscopy and differential scanning calorimetry （DSC）. The values of their density, surface tension and refractive index were measured at （298.15 ± 0.05） K. Since the AAILs can form strong hydrogen bonds with water, small amounts of water are difficult to remove from the AAILs by common methods. In order to eliminate the effect of the impurity water, the standard addition method （SAM） was applied to these measurements. A new concept which is called the ionic parachor has been put forward. The [Cn mim]＋ cations were treated as a group of reference ions and the individual values of their ionic parachor were evaluated in terms of an extrathermodynamic assumption. Then, using the values of the ionic parachor of reference ions, the parachor, surface tension y and refractive index no of the ionic liquids investigated in this work were estimated. The estimated values correlate quite well with the corresponding experimental values.

关键词： ionic liquids ionic parachor glycine density surface tension extrathermodynamic assumption

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Photoreduction adjusted surface oxygen vacancy of Bi_(2)MoO_(6) for boosting photocatalytic redox performance

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Frontiers of Chemical science and Engineering 2023年第12期17卷 1937-1948页

作者： Tie Shi Hailong Jia Yanmei Feng Bo Gong Daimei Chen Yu Liang Hao Ding Kai Chen Derek Hao Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes National Laboratory of Mineral MaterialsSchool of Materials Science and TechnologyChina University of GeosciencesBeijing 100083China School of Materials science and Technology Shenyang University of Chemical TechnologyShenyang 110142China Collaborative Innovation Center of Atmospheric Environment and Equipment Technology Jiangsu Key Laboratory of Atmospheric Environment Monitoringand Pollution Control School of Environmental Science and EngineeringNanjing University of Information Science and TechnologyNanjing 210044China Centre for Technology in Water and Wastewater(CTWW) School of Civil and Environmental EngineeringUniversity of Technology Sydney(UTS)NSW 2007Australia

In this study, Bi_(2)MoO_(6) with adjustable rich oxygen vacancies was prepared by a novel and simple solvothermal-photoreduction method which might be suitable for a large-scale production. The experiment results show that Bi_(2)MoO_(6) with rich oxygen vacancies is an excellent photocatalyst. The photocatalytic ability of BMO-10 is 0.3 and 3.5 times higher than that of the pristine Bi_(2)MoO_(6) for Rhodamine B degradation and Cr(VI) reduction, respectively. The results display that the band energy of the samples with oxygen vacancies was narrowed and the light absorption was broadened. Meanwhile, the efficiency of photogenerated electron-holes was increased and the separation and transfer speed of photogenerated carriers were improved. Therefore, this work provides a convenient and efficient method to prepare potential adjustable oxygen vacancy based photocatalysts to eliminate the pollution of dyes and Cr(VI) in water.

关键词： Bi_(2)MoO_(6) oxygen vacancies photoreduction Cr(VI) RhB

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Forced vibration control of an axially moving beam with an attached nonlinear energy sink

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Acta Mechanica Solida Sinica 2017年第6期30卷 674-682页

作者： Ye-Wei Zhang Shuai Hou Ke-Fan Xu Tian-Zhi Yang Li-Qun Chen Department of Astronautics Shenyang Aerospace University Shenyang 110136 China Shanghai Institute of Applied Mathematics and Mechanics Shanghai Uniuersity Shanghai 200072 China Department of Mechanics Shanghai University Shanghai 200444 China

This paper investigates a highly efficient and promising control method for forced vibration control of an axially moving beam with an attached nonlinear energy sink（NES）.Because of the axial velocity,external force and external excitation frequency,the beam undergoes a high-amplitude *** Galerkin method is applied to discretize the dynamic equations of the beam–NES *** steady-state responses of the beams with an attached NES and with nothing attached are acquired by numerical ***,the fast Fourier transform（FFT）is applied to get the amplitude–frequency *** the perspective of frequency domain analysis,it is explained that the NES has little effect on the natural frequency of the *** confirm that NES has a great potential to control the excessive vibration.

关键词： Forced vibration Axially moving beam FFT Nonlinear energy sink(NES) External excitation frequency

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Variation characteristic of drilling force and influence of cutting parameter of SiCp/Al composite thin-walled workpiece

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Advances in Manufacturing 2019年第3期7卷 288-302页

作者： Shu-Tao Huang Chao Li Li-Fu Xu Lin Guo Xiao-Lin Yu School of Automobile and Traffic Shenyang Ligong UniversityShenyang 110159People's Republic of China School of Mechanical Engineering Dalian University of TechnologyDalian 116024LiaoningPeople's Republic of China School of Mechanical Engineering Shenyang Ligong UniversityShenyang 110159People's Republic of China

In this paper,the variation characteristic of the drilling force,and the influences of cutting speed,feed rate,and workpiece thickness on the drilling force,were eval・uated when drilling a silicon carbide particle reinforced aluminum matrix(SiCp/Al)composite thin-walled workpiece with a high volume *** the condition that the workpiece thickness was less than the drill tip height,three characteristic stages of drilling force variation were *** results indicate that there is a sign币cant difference between the variations in the drilling force when drilling a thin-walled workpiece compared to thick-walled *** the chisel edge drills out the lower surface of the workpiece,there is an abrupt decrease in the thrust forces of the thin-walled and thick-walled *** addition,there is an abrupt decrease in the torque of the thick-walled workpiece,whereas that of the thinwalled workpiece *** to the thickness of the thin-walled workpiece,the instant of the abrupt decrease in the thrust force may lead or lag behind the theoretical instant at which the chisel edge reaches the lower surface of the workpiece without *** drilling a thin-walled hole,the cutting speed has a slight influence on the thrust force,and there is a slight increase in the torque in accordance with an increase in the cutting *** thrust force and torque increase in accordance with an increase in the feed *** drilling a thinwalled workpiece with a thickness of 1 mm,the critical thickness of workpiece cracking decreases in accordance with an increase in the cutting speed,and increases in accordance with an increase in the feed *** drilling a thin-walled workpiece with a thickness of 0.5 mm,the concave deformation of the workpiece and the critical thickness of the workpiece cracking increase in accordance with an increase in the feed ***,the increment in the critical thickness of the workpiece cracking is less than that in

关键词： SiCp/Al composites Thin-walled workpiece Drilling Drilling force

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低温耐磨的CoCrNi多主元合金（英文）

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science Bulletin 2024年第2期 227-236页

作者：任越周青华东鹏黄卓斌李钰龙贾茜 Peter Gumbsch Christian Greiner 王海丰刘维民 State Key Laboratory of Solidification Processing Center of Advanced Lubrication and Seal Materials Northwestern Polytechnical University Institute for Applied Materials Karlsruhe Institute of Technology IAM-ZM Micro Tribology Center μTC Karlsruhe Institute of Technology Fraunhofer IWM State Key Laboratory of Solid Lubrication Lanzhou Institute of Chemical Physics Chinese Academy of Sciences

Traditional high strength engineering alloys suffer from serious surface brittleness and inferior wear performance when servicing under sliding contact at cryogenic temperature. Here, we report that the recently emerging CoCrNi multi-principal element alloy defies this trend and presents dramatically enhanced wear resistance when temperature decreases from 273 to 153 K, surpassing those of cryogenic austenitic steels. The temperature-dependent structure characteristics and deformation mechanisms influencing the cryogenic wear resistance of CoCrNi are clarified through microscopic observation and atomistic simulation. It is found that sliding-induced subsurface structures show distinct scenarios at different deformation temperatures. At cryogenic condition, significant grain refinement and a deep plastic zone give rise to an extended microstructural gradient below the surface, which can accommodate massive sliding deformation, in direct contrast to the strain localization and delamination at 273 ***, the temperature-dependent cryogenic deformation mechanisms(stacking fault networks and phase transformation) also provide additional strengthening and toughening of the subsurface material. These features make the CoCrNi alloy particularly wear resistant at cryogenic conditions and an excellent candidate for safety–critical applications.

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Hydrogen bond promoted thermal stability enhancement of acetate based ionic liquid

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Chinese Journal of Chemical Engineering 2020年第5期28卷 1293-1301页

作者： Ling Zhang Ligang Wei Shangru Zhai Dingwei Zhao Jian Sun Qingda An Faculty of Light Industry and Chemical Engineering Dalian Polytechnic UniversityDalian 116034China Key Laboratory of Molecular Medicine and Biotherapy School of Life ScienceBeijing Institute of TechnologyBeijing100081China

Acetate-based imidazolium ionic liquids(ILs)are of great importance and widely applied in biomass processing and engineering but under stability issue due to the structure self–rearrangement induced by C2–H deprotonation,by which the IL based biomass processing will be ***,we demonstrated that the thermal stability of normal acetate-based imidazolim[C8C1Im][OAc]could be significantly improved by changing its cation and anion environment with the presence of 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide IL([C4C1Im][NTf2]).When the molar fraction of[C8C1Im][OAc]was 0.3,the thermal stability of[C8C1Im][OAc]could be significantly improved(ΔT5%dec=+43°C).Detailed information obtained from thermal gravimetric analysis(TGA)and nuclear magnetic resonance(NMR)revealed that the addition of[C4C1 Im][NTf2]played a significant role in enhancing the thermal stability of[C8C1Im][OAc].It was proposed that the formation of an anion–π+structure network between[C8C1 Im][OAc]and[C4C1Im][NTf2]via strong hydrogen bond interactions greatly affects the environment of hydrogen atom in the imidazolium ring of each IL.

关键词： Imidazolium salt Binary ionic liquids Thermal stability Hydrogen bond interactions

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