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Rare Metals 2024年第4期43卷 1570-1579页

作者： Gang Dong Cong Huang Fei-Yang Chen Xue-Qin Liu Zhen Li Xiao-Li Su Tao Zeng Yun-Xia Chen Yi-Huang Chen Yang Wang school of materials Science and engineering Jingdezhen Ceramic University Faculty of materials Science and chemistry China University of Geosciences College of chemistry and materials engineering Wenzhou University

Given the clean and inexhaustible solar energy from solar light,photocatalytic ammonia synthesis is extremely appealing.However,high electron-hole recombination rates and insufficient active sites severely limited N2 photoreaction reduction.Herein,we designed and fabricated FeCu alloy nanoparticles anchored on carbon nitride nanosheets with excellent photocatalyt ic ammonia synthesis performance.As a coupler between Fe and carbon nitride,Cu promotes the separation of photogenerated charge carriers in carbon nitride under solar light irradiation,and renters the semiconductor a forceful electron donor for the Fe active sites.The accumulated electrons at Fe sites furtherly facilitated the adsorption and activation of the molecular nitrogen.Besides,the uniform dispersed FeCu alloy nanoparticles were on carbon nitride nanosheets enhanced the stability of photocataly tic nitrogen reduction reaction,making the artificial photocataly tic ammonia synthesis more sustainable for application.This work highlights that a direct electron transfer channel can be used to regulate the photochemical nitrogen fixation network.

关键词： Photocatalytic N 2 fixation Carbon nitride FeCu alloy Active sites Hydrogenation pathway

The homogenous growth of Co-based coordination compound on graphene nanosheet for high-performance K-organic battery and its reaction mechanism

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Rare Metals 2024年第4期43卷 1622-1634页

作者： Qian-Qian Peng Yi-Ting Wang Shuo Qi Yao Xiao Yong Wang Shuang-Qiang Chen school of Environmental and Chemical engineering Shanghai University school of chemistry and materials engineering Wenzhou University

Metal coordination compounds（MCCs） are gaining popularity for potassium-ion batteries（PIBs）owing to their tuneable structure,multiple reaction sites,low cost and unique morphology.However,they are generally subjected to intrinsic features of the sluggish ionic diffusion coefficient,low electronic conductivity and slow kinetics.Herein,a new MCC material of cobalt-1,3,5-trioxy-2,4,6-triamino-benzo（Co-TB） coordination compound was synthesized and homogenously grown on the surface of graphene nanosheets（GNS）,forming a Co-TB@GNS composite with enhanced electronic conductivity and flexible capability.Benefiting from the overall enhanced conductivity,high surface area and abundant activated K-storage sites,Co-TB@GNS electrodes have exhibited superior cycling performance with high reversible capacities(312 mAh·g-1after 100 cycles at 100 mA·g-1,224 mAh·g-1after 500 cycles at 1 A·g-1) and better rate performances compared with the pure Co-TB compound when served as PIB's anodes.Furthermore,multiple in-situ measurement techniques have jointly confirmed that the organic functional groups（C=O,C=N and C=C of benzene rings） and Co2+in Co-TB are the main reversible K-storage sites,including in-situ Fourier transform infrared spectroscopy（FTIR） and X-ray diffraction（XRD）,and partial capacity contribution is originated from GNS by the apparent K-storage behavior in the in-situ XRD pattern,proving the possibility of K-storage for metal-organic materials.

关键词： Metal coordination compounds Potassium-ion battery Cobalt coordination compound K-storage mechanism

Catalytic asymmetric(3 + 3) cycloaddition between different 2-indolylmethanols

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Science China chemistry 2024年第8期67卷 2629-2636页

作者： Tianzhen Li Sijia Liu Shufang Wu Qi Cheng Qun Chen Yinchun Jiao Yuchen Zhang Feng Shi school of Petrochemical engineering School of Materials Science & Engineering Changzhou University Research Center of Chiral Functional Heterocycles School of Chemistry and Materials Science Jiangsu Normal University school of chemistry and Chemical engineering Hunan University of Science and Technology school of chemistry and Chemical engineering Henan Normal University

The catalytic asymmetric(3 + 3) cycloaddition between different 2-indolylmethanols has been established, in which a series of chiral indole-fused six-membered heterocycles were constructed in high yields with excellent enantioselectivities. This work not only has established the first catalytic asymmetric cycloaddition between different 2-indolylmethanols but also provided a powerful strategy for constructing enantioenriched indole-fused six-membered rings. Additionally, biological evaluation discovered some products with promising antitumor activities. Notably, theoretical calculations performed on the reaction pathway and activation mode provide an in-depth understanding of this catalytic asymmetric(3 + 3) cycloaddition among different 2-indolylmethanols, which will advance the understanding of the chemistry of indolylmethanols.

关键词： 2-indolylmethanol asymmetric organocatalysis chiral phosphoric acid cycloaddition enantioselectivity

One dimensional CeO_(2) nanorods/poly(ethylene oxide) solid composite electrolyte for all-solid-state lithium-ion batteries

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Journal of Rare Earths 2024年第3期42卷 570-577,I0005页

作者： Yudi Guo Erqing Zhao Xiaofang Zhao Shuailei Liu school of chemistry and materials engineering Xinxiang UniversityXinxiang453003China school of chemistry and Chemical engineering Henan Institute of Science and TechnologyXinxiang453003China

The research of poly(ethylene oxide)(PEO)-based solid composite electrolyte with high ionic conductivity and excellent interfacial stability is the key to the development of all-solid-state lithium-ion batteries(ASSLIBs). Herein, uniform nanorod structured CeO_(2) fillers were controllably synthesized by electrospinning, which were subsequently filled into PEO polymer to prepare CeO_(2)/PEO solid composite electrolyte. The addition of CeO_(2) nanorods can reduce both the glass transition temperature and the melting point of PEO polymer, and also interact with PEO and lithium bis(trifluoromethanesulphonyl)imide(LITFSI) by Lewis acid—base reaction. Therefore, the solid composite electrolyte exhibits a high ionic conductivity of 4.52 × 10^(-4)S/cm, a wide electrochemical stability window of about 4.8 V, and a good interfacial stability with Li at 55℃. Moreover, the LiFePO_4/Li ASSLIB divulges the discharging specific capacity of 165, 162, 156 and 146 mA,h/g at 0.2, 0.5, 1 and 2 C, respectively, and achieves the capacity retention of 90.3% after 150 cycles at 0.5 C. Consequently, one dimensional CeO_(2) nanorods can be considered as an alternative filler for polymeric solid electrolyte.

关键词： Poly(ethylene oxide) Solid composite electrolyte CeO_(2)nanorods Ionic conductivity Rare earths

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Recent advances in Ir/Ru-based perovskite electrocatalysts for oxygen evolution reaction

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Rare Metals 2024年第7期43卷 2891-2912页

作者： Zhi-Qi Jiang Cheng-Zhen Fan Jun-Yu Pan Li Shao Hao Chen Erum Pervaiz Yan Dong Tong-Zhou Wang Xue-Rong Zheng Ji-Hong Li Yi-Da Deng school of materials Science and engineering Hainan University Department of Chemical engineering School of Chemical and Materials Engineering (SCME)National University of Sciences & Technology (NUST) Key Laboratory of Advanced Energy materials chemistry (Ministry of Education) Nankai University

Oxygen evolution reaction(OER) is a kinetically harsh four-electron anode reaction that requires a large overpotential to provide current and is of great importance in renewable electrochemical technique.Ir/Rubased perovskite oxides hold great significance for application as OER electrocatalysts,due to that their multimetal-oxide forms can reduce the use of noble metals,and their compositional tunability can modulate the electronic structure and optimize OER performance.However,high operating potentials and corrosive environments pose a serious challenge to the development of durable Ir-based and Ru-based perovskite electrocatalysts.Tremendous efforts have been dedicated to improving the Ir/Ru-based perovskite activity to enhance the efficiency;however,progress in improving the durability of Ir/Ru-based perovskite electrocatalysts has been rather limited.In this review,the recent research progress of Ir/Ru-based perovskites is reviewed from the perspective of heteroatom doping,structural modulation,and formation of heterostructures.The dissolution mechanism studies of Ir/Ru and experimental attempts to improve the durability of Ir/Ru-based perovskite electrocatalysts are discussed.Challenges and outlooks for further developing Ru-and Irbased perovskite oxygen electrocatalysts are also presented.

关键词： Oxygen evolution reaction Ir/Ru-based perovskites Stability Electrocatalysts

On-surface synthesis and characterization of polyynic carbon chains

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National Science Review 2024年第3期11卷 192-199页

作者： Wenze Gao Wei Zheng Luye Sun Faming Kang Zheng Zhou Wei Xu Interdisciplinary materials Research Center School of Materials Science and Engineering Tongji University

Carbyne, an elusive sp-hybridized linear carbon allotrope, has fascinated chemists and physicists for decades. Due to its high chemical reactivity and extreme instability, carbyne was much less explored in contrast to the sp2-hybridized carbon allotropes such as graphene. Herein, we report the on-surface synthesis of polyynic carbon chains by demetallization of organometallic polyynes on the Au（111） surface;the longest one observed consists of ～60 alkyne units（120 carbon atoms）. The polyynic structure of carbon chains with alternating triple and single bonds was unambiguously revealed by bond-resolved atomic force microscopy. Moreover, an atomically precise polyyne, C14, was successfully produced via tip-induced dehalogenation and ring-opening of the decachloroanthracene molecule(C14Cl10) on a bilayer NaCl/Au（111） surface at 4.7 K, and a band gap of 5.8 eV was measured by scanning tunnelling spectroscopy,in a good agreement with the theoretical HOMO–LUMO gap（5.48 eV）.

关键词： polyyne scanning probe microscopy carbon allotrope on-surface synthesis organometallic polyyne

Effects of combustion temperature on the optical properties of brown carbon from biomass burning

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Journal of Environmental Sciences 2024年第3期137卷 302-309页

作者： Peng Gao Rule Deng Song Jia Yue Li Xuefei Wang Qian Xing school of chemistry Sciences University of Chinese Academy of SciencesBeijing 100049China College of chemistry and materials engineering Beijing Technology and Business UniversityBeijing 100048China

Biomass burning has been known as one of main sources of Brown Carbon(BrC)in atmosphere.In this study,by controlling the combustion temperature at 250℃,350℃,and 450℃,the methanol soluble organic carbon(MSOC)and methanol insoluble carbon(MISC)from pine wood burning was collected by impinger.UV–Vis,excitation emission matrix(EEM),TEM and FTIR spectra were applied to investigate the properties of BrC collected.For MSOC at 250℃ and 350℃,all the spectral profiles of UV–Vis absorption and excitation emission matrix are almost the same,while the EEM of MSOC at 450℃ are different from that of the other two.For MISC fuorescence was observed only in the case of 450℃.In the FTIR spectra,with the temperature increasing the peaks associated to the oxygen-contained functions was weakened,indicating the formation of the fuorophores with larger conjugated system,especially aromatic hydrocarbons.Our results show that biomass combustion at low temperature produces more oxygen-riched BrC,which possesses relatively lower light absorption,while at high temperature produces more aromatics hydrocarbons with relatively strong light absorption.The results of this work are helpful to trace the source of brown carbon and optimize biomass energy utilization.

关键词： Biomass burning Combustion temperature Methanol-soluble brown carbon EEM Impinger

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Cu,N codoped carbon nanosheets encapsulating ultrasmall Cu nanoparticles for enhancing selective 1,2-propanediol oxidation

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Journal of Energy chemistry 2024年第4期91卷 27-35页

作者： Yonghai Feng Min Yu Minjia Meng Lei Liu Dewei Rao Institute for Advanced materials School of Materials Science and EngineeringJiangsu UniversityZhenjiang 212013JiangsuChina school of chemistry and Chemical engineering Jiangsu UniversityZhenjiang 212013JiangsuChina

In the selective oxidation of biomass-based 1,2-propanediol(PDO)with oxygen as the terminal oxidant,it is challenging to improve the lactic acid(LA)selectivity for nonnoble metal nanoparticles(NPs)due to their limited oxygen reduction rate and easy C-C cleavage.Given the high economic feasibility of nonnoble metals,i.e.,Cu,in this work,copper and nitrogen codoped porous carbon nanosheets encapsulating ultrafine Cu nanoparticles(Cu@Cu-N-C)were developed to realize highly selective of PDO oxidation to LA.The carbon-encapsulated ultrasmall Cu^(0)NPs in Cu@Cu-N-C have high PDO dehydrogenation activity while N-coordinated Cu(Cu-N)sites are responsible for the high oxygen reduction efficacy.Therefore,the performance of catalytic PDO conversion to LA is optimized by a proposed pathway of PDO→hydroxylacetone→lactaldehyde→LA.Specifically,the enhanced LA selectivity is 88.5%,and the PDO conversion is up to 75.1%in an O_(2)-pressurized reaction system(1.0 MPa O_(2)),superior to other Cu-based catalysts,while in a milder nonpressurized system(O_(2)flow rate of 100 mL min-1),a remarkable LA selectivity(94.2%)is obtained with 39.8%PDO conversion,2.2 times higher than that of supported Au nanoparticles(1%Au/C).Moreover,carbon encapsulation offers Cu@Cu-N-C with strong leaching resistance for better recycling.

关键词： Selective oxidation Copper and nitrogen doped carbon 1,2-Propanediol Ultrasmall Cu nanoparticles Lactic acid

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Precipitation kinetics and strengthening of M23C6 in novel G115 martensitic steel:Utilizing secondary normalizing

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Progress in Natural Science:materials International 2024年第2期34卷 396-407页

作者： Chengxian Zhang Zhi Yuan Qiuzhi Gao Qingshuang Ma Hailian Zhang Jing Bai Huijie Zhang Liming Yu Huijun Li school of materials Science and engineering Northeastern University school of Resources and materials Northeastern University at Qinhuangdao school of materials Science & engineering Tianjin University school of Mechanical Materials and Mechatronic Engineering University of Wollongong

G115 martensitic steel is anticipated to be one of the preferred candidate materials in ultra-super critical(USC)power plants with steam temperatures above 650℃.Microstructure evolutions and mechanical properties of G115 martensitic steel after applying various heat treatment processes were investigated.The results demonstrate that the main precipitate in G115 martensitic steel after applying various heat treatment processes is M23C6 phase with Cr enrichment.The time required for M23C6 phase precipitation decreases with increasing secondary normalizing temperature and the extension in holding time according to its precipitation-temperature-time(PTT)curves.Volume fraction of M23C6 phase increases with increasing secondary normalizing temperature and holding time,which strengthens the inhibitory effect of precipitates on dislocations recovery and laths growth.Therefore,G115 martensitic steel can obtain the best mechanical properties after applying the highest secondary normalizing temperature and the longest holding time.In the current work,the excellent strength of G115 martensitic steel mainly derives from precipitates strengthening and laths strengthening.

关键词： G115 martensitic steel M23C6 phase Precipitation kinetics Secondary normalizing Strengthening mechanisms

Fine structure and facet analyses of tunnel-structured FeOOH nanocrystals

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Progress in Natural Science:materials International 2024年第1期34卷 172-177页

作者： Xuemei Zeng Yanshuai Li Wenjun Song Yun Li Dewu Yin Yifei Yuan Kun He College of chemistry and materials engineering Wenzhou University

The development of energy storage systems in the future relies on identifying suitable target materials and synthesizing target materials with controllable physicochemical properties to unlock their electrochemical contributions. Based on the structure-property-performance relationship established in materials science, it is crucial to determine the fine structure of key functional materials. Among these materials, tunnel-structured β-FeOOH is widely studied due to its low-cost, decent performance and environmental friendliness; yet, its fine structure in terms of the atomic framework and surface configuration has not been well understood. In this work, we successfully synthesized β-FeOOH nanorods and analyzed their crystallographic features via transmission electron microscopy(TEM). By combining ultramicrotome and aberration-corrected scanning TEM with atomic resolution,we first experimentally revealed the structural details of β-FeOOH featuring 1 × 1 tunnels and 2 × 2 tunnels along the c-axis([001]), the same as the nanorod growth direction. The dominant exposed facets of β-FeOOH nanorods were further revealed to be {010}. Such fine structural elucidation unveils the long-existing mystery in this material system, which is expected to contribute to structural/compositional engineering toward functionality optimization in the near future.

关键词： β-FeOOH tunnel Anisotropic growth Atomic resolution Nanorod Energy storage