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Wuhan University Journal of Natural Sciences 2024年第2期29卷 165-176页

作者： HU Dandan XUE Yangfan LIU Bo WU Yongjuan LI Zichen school of chemistry&chemical engineering Shaanxi Xueqian Normal UniversityXi'an 710100ShaanxiChina Safe college Xi􀆳an University of Science and TechnologyXi'an 710054ShaanxiChina

In this work,porous biochar(MN-TRB_(750))was fabricated via direct pyrolysis of tea residue(TR)and Mg(NO_(3))_(2)·6H_(2)O(MN).The as-synthesized MN-TRB_(750) reached a specific surface area of 839.54 m^(2)·g^(-1)and an average pore size of 3.75 nm with multi-level pore *** decreased TR's carbonization temperature and promoted the aromatics extent,pore structure for the frizzly flake-like *** B(RhB)was chosen as the adsorbate to explore the removal performance of organic dyes in this *** results indicated that the maximum adsorption capacity of RhB on MN-TRB_(750) at 20℃ is up to 809.0 mg·g^(-1)with isotherms fitted well to Freundlich and Dubinin-Radushkevic *** adsorption kinetics followed pseudo-second-order and Elovich models with an equilibrium adsorption capacity of 757.6 mg·g^(-1)as the initial concentration of RhB is 260 mg·L^(-1).High pore filling,hydrogen bond,π-πinteraction determined the adsorption of RhB onto MN-TRB850 through a multi-active center and exothermic chemical sorption process.

关键词： Mg(NO_(3))_(2)·6H_(2)O porous biochar mechanism rhodamine B adsorption

Coupling of BiOCl Ultrathin Nanosheets with Carbon Quantum Dots for Enhanced Photocatalytic Performance

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Transactions of Tianjin University 2024年第3期30卷 211-220页

作者： Pin Song Xiaoyu Fang Wei Jiang Yuyang Cao Daobin Liu Shiqiang Wei Jun Du Lang Sun Lei Zhao Song Liu Yuzhu Zhou Jun Di Chade Lv Bijun Tang Jiefu Yang Tingting Kong Yujie Xiong Key Laboratory of Functional Molecular Solids Ministry of EducationAnhui Engineering Research Center of Carbon NeutralityCollege of Chemistry and Materials ScienceAnhui Normal UniversityWuhu 241000China National Synchrotron Radiation Laboratory CAS Center for Excellence in NanoscienceSchool of Chemistry and Materials ScienceUniversity of Science and Technology of ChinaHefei 230029China school of chemistry and chemical engineering National Special Superfi ne Powder Engineering Research CenterNanjing University of Science and TechnologyNanjing 210094China MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage School of Chemistry and Chemical EngineeringHarbin Institute of TechnologyHarbin 150001China school of Materials Science&engineering Nanyang Technological UniversitySingapore 639798Singapore

Over the past few decades,photocatalysis technology has received extensive attention because of its potential to mitigate or solve energy and environmental pollution *** novel materials with outstanding photocatalytic activities has become a research hotspot in this *** this study,we prepared a series of photocatalysts in which BiOCl nanosheets were modified with carbon quantum dots(CQDs)to form CQDs/BiOCl composites by using a simple solvothermal *** photocatalytic performance of the resulting CQDs/BiOCl composite photocatalysts was assessed by rhodamine B and tetracycline degradation under visible-light *** with bare BiOCl,the photocatalytic activity of the CQDs/BiOCl composites was significantly enhanced,and the 5 wt%CQDs/BiOCl composite exhibited the highest photocatalytic activity with a degradation efficiency of 94.5%after 30 min of ***,photocatalytic N_(2)reduction performance was significantly improved after introducing *** 5 wt%CQDs/BiOCl composite displayed the highest photocatalytic N_(2)reduction performance to yield NH_3(346.25μmol/(g h)),which is significantly higher than those of 3 wt%CQDs/BiOCl(256.04μmol/(g h)),7 wt%CQDs/BiOCl(254.07μmol/(g h)),and bare BiOCl(240.19μmol/(g h)).Our systematic characterizations revealed that the key role of CQDs in improving photocatalytic performance is due to their increased light harvesting capacity,remarkable electron transfer ability,and higher photocatalytic activity sites.

关键词： Carbon quantum dots BiOCl Rhodamine B Tetracycline Photocatalysis

Comprehensive understanding of the thriving electrocatalytic nitrate/nitrite reduction to ammonia under ambient conditions

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Journal of Energy chemistry 2024年第5期92卷 459-483页

作者： Xinying Zhao Yuzhuo Jiang Mengfan Wang Yunfei Huan Qiyang Cheng Yanzheng He Tao Qian Chenglin Yan Collaborative Innovation Center of Suzhou Nano Science and Technology College of EnergySoochow UniversitySuzhou 215006JiangsuChina school of chemistry and chemical engineering Nantong UniversityNantong 226019JiangsuChina school of Petrochemical engineering Changzhou UniversityChangzhou 213164JiangsuChina

Ammonia(NH_(3))is a multifunctional compound that is an important feedstock for the agricultural and pharmaceutical industries and attractive energy storage *** present,NH_(3)synthesis is highly dependent on the conventional Haber–Bosch process that operates under harsh conditions,which consumes large quantities of fossil fuels and releases a large amount of carbon *** an alternative,electrosynthesis is a prospective method for producing NH_(3)under normal temperature and pressure *** electrocatalytic nitrogen reduction to ammonia has attracted considerable attentions,the low solubility of N_(2)and high N≡N cracking energy render the achievements of high NH_(3) yield rate and Faradaic efficiency *** and nitrite(NO_(x)^(-))are common N-containing *** to their high solubilities and low dissociation energy of N=O,NO_(x)^(-)−are ideal raw materials for NH_(3) ***,electrocatalytic NO_(x)^(-)−reduction to NH_(3)(eNO_(x)RR)is a prospective strategy to simultaneously realise environmental protection and NH_(3) *** review offers a comprehensive understanding of the thriving eNO_(x)RR under ambient *** first,the popular theory and mechanism of eNO_(x)RR and a summary of the measurement system and evaluation criteria are ***,various strategies for developing NO_(x)−reduction catalysts are systematically presented and ***,the challenges and possible prospects of electrocatalytic NO_(x)^(-1) reduction are outlined to facilitate energy-saving and environmentally friendly large-scale synthesis of NH_(3) in the future.

关键词： Electrocatalytic nitrate reduction Electrocatalytic nitrite reduction Ammonia synthesis Pollutant removal Electrosynthesis

Synthesis of biheteroaryls via 2-methyl quinoline C(sp^(3))-H functionalization under metal-free conditions

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Green Synthesis and Catalysis 2024年第1期5卷 73-76页

作者： Dahan Wang Yuhan Yang Fuhong Xiao Jinbing Liu Guojiang Mao Guo-Jun Deng Key Laboratory of Environmentally Friendly chemistry and Application of Ministry of Education Hunan Province Key Laboratory of Green Organic Synthesis and ApplicationCollege of ChemistryXiangtan UniversityXiangtan 411105China Department of Food and chemical engineering Shaoyang UniversityShaoyang 422100China school of chemistry and chemical engineering Henan Normal UniversityXinxiang 453007China

An acetic acid-promoted C(sp^(3))-H functionalization of 2-methyl quinoline,enaminoesters and elemental sulfur for the synthesis of 3,4,5-trisubstituted isothiazoles under metal-free conditions has been *** approach provides viable access to various 5-(quinolin-2-yl)isothiazoles in moderate to good yields with good functional group ***,the success of the gram-scale reaction gives this reaction a great potential application.

关键词： C(sp^(3))-H functionalization Multicomponent reactions Biheteroaryls Elemental sulfur Metal-free

Cu-catalyzed enantioselective assembly of axially chiral allylic boronates

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Science China chemistry 2024年

作者： Shuai Wang Jianbo Liu Wenyue Ma Qiuling Song Key Laboratory of Molecule Synthesis and Function Discovery Fujian Province University College of Chemistry at Fuzhou University State Key Laboratory of Organometallic chemistry Shanghai Institute of Organic Chemistry Chinese Academy of Sciences school of chemistry and chemical engineering Henan Normal University

Highly enantioselective construction of axially chiral cyclohexylidenes is difficult and challenging due to their structural peculiarities. The development of efficient method for the assembly of novel axially chiral cyclohexylidenes becomes particularly important in axial chirality. Chiral allylborons have become a focus of interest in chemical community as an important synthon as well as a backbone structure, yet an efficient and practical synthetic method for the synthesis of axially chiral allylborons have not been disclosed so far. Herein, we report a copper-catalyzed strategy which could readily access enantiopure axially chiral allylborons under mild conditions. The obtained axially chiral allylborons can also be subjected to a number of subsequent transformations as well as late modification of drug molecules, thus demonstrating the validity of the developed method.

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Fe-doped Co_(3)O_(4) nanowire strutted 3D pinewood-derived carbon: A highly selective electrocatalyst for ammonia production via nitrate reduction

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Nano Research 2024年第4期17卷 2276-2282页

作者： Xuwei Liu Chaozhen Liu Xun He Zhengwei Cai Kai Dong Jun Li Xiaoya Fan Ting Xie Xiya Yang Yonglan Luo Dongdong Zheng Shengjun Sun Sulaiman Alfaifi Feng Gong Xuping Sun Institute of Fundamental and Frontier Sciences University of Electronic Science and Technology of ChinaChengdu 610054China Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education School of Energy and EnvironmentSoutheast UniversityNanjing 211189China college of chemistry Chemical Engineering and Materials ScienceShandong Normal UniversityJinan 250014China chemistry Department Frontier of ScienceKing Abdulaziz UniversityJeddah 21589Saudi Arabia

Nitrate(NO_(3)^(-)),a nitrogen-containing pollutant,is prevalent in aqueous solutions,contributing to a range of environmental and health-related *** electrocatalytic reduction of NO_(3)^(-)holds promise as a sustainable approach to both eliminating NO_(3)^(-)and generating valuable ammonia(NH_(3)).Nevertheless,the reduction reaction of NO_(3)^(-)(NO_(3)^(-)RR),involving 8-electron transfer process,is intricate,necessitating highly efficient electrocatalysts to facilitate the conversion of NO_(3)^(-)to NH_(3).In this study,Fe-doped Co_(3)O_(4) nanowire strutted three-dimensional(3D)pinewood-derived carbon(Fe-Co_(3)O_(4)/PC)is proposed as a high-efficiency NO_(3)^(-)RR electrocatalyst for NH_(3) *** within 0.1 M NaOH containing NO_(3)^(-),Fe-Co_(3)O_(4)/PC demonstrates exceptional performance,obtain an impressively large NH_(3) yield of 0.55 mmol·h^(-1)·cm^(-2) and an exceptionally high Faradaic efficiency of 96.5%at-0.5 V,superior to its Co_(3)O_(4)/PC counterpart(0.2 mmol·h^(-1)·cm^(-2),73.3%).Furthermore,the study delves into the reaction mechanism of Fe-Co_(3)O_(4) for NO_(3)^(-)RR through theoretical calculations.

关键词： Fe-doped Co_(3)O_(4) nanowire pinewood-derived carbon electrocatalytic NO_(3)-reduction NH_(3) synthesis density functional theory

Stabilizing zinc anode using zeolite imidazole framework functionalized separator for durable aqueous zinc-ion batteries

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Journal of Energy chemistry 2024年第3期90卷 23-31,I0003页

作者： Weisong Zhang Xinyan Zhu Ling Kang Ziyu Peng Jing Zhu Liang Pan Lei Dai Shude Liu Ling Wang Yongguang Liu Zhangxing He school of chemical engineering North China University of Science and TechnologyTangshan 063009HebeiChina Shanghai Key Laboratory of Multidimensional Information Processing East China Normal UniversityShanghai 201620China college of Textiles Donghua UniversityShanghai 201620China

Aqueous zinc-ion batteries(AZIBs) hold great promise as a viable alternative to lithium-ion batteries owing to their high energy density and environmental ***,AZIBs are consistently plagued by the formation of zinc dendrites and concurrent side reactions,which significantly diminish their overall service life,In this study,the glass fiber separator(GF) is modified using zeolite imidazole salt framework-8(ZIF-8),enabling the development of efficient ***-8,which is abundant in nitrogen content,efficiently regulates the desolvation of [Zn(H_(2)O)_(6)]^(2+) to inhibit hydrogen ***,it possesses abundant nanochannels that facilitate the uniform deposition of Zn~(2+) via a localized action,thereby hindering the formation of *** insulating properties of ZIF-8 help prevent Zn^(2+) and water from trapping electron reduction at the layer surface,which reduces corrosion of the zinc ***,ZIF-8-GF achieves the even transport of Zn^(2+) and regulates the homogeneous deposition along the Zn(002) crystal surface,thus significantly enhancing the electrochemical performance of the AZIBs,In particular,the Zn|Zn symmetric cell with the ZIF-8-GF separator delivers a stable cycle life at0.5 mA cm^(-2) of 2300 *** Zn|ZIF-8-GF|MnO_(2) cell exhibits reduced voltage polarization while maintaining a capacity retention rate(93.4%) after 1200 cycles at 1.2 A g^(-1) The unique design of the modified diaphragm provides a new approach to realizing high-performance AZIBs.

关键词： Aqueous zinc-ion batteries Separators modifications ZIF-8 Zn deposition Dendrite-free

Manipulating d-d orbital hybridization induced by Mo-doped Co_(9)S_(8) nanorod arrays for high-efficiency water electrolysis

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Journal of Energy chemistry 2024年第6期93卷 592-600,I0015页

作者： Xue Zhou Jing Li Guangyao Zhou Weiran Huang Yucan Zhang Jun Yang Huan Pang Mingyi Zhang Dongmei Sun Yawen Tang Lin Xu Jiangsu Key Laboratory of New Power Batteries Jiangsu Collaborative Innovation Centre of Biomedical Functional MaterialsSchool of Chemistry and Materials ScienceNanjing Normal UniversityNanjing 210023JiangsuChina 'college of Science Jinling Institute of TechnologyNanjing 211169JiangsuChina State Key Laboratory of Multiphase Complex Systems Institute of Process EngineeringChinese Academy of SciencesBeijing 100190China Nanjing IPE Institute of Green Manufacturing Industry Nanjing 211100JiangsuChina school of chemistry and chemical engineering Yangzhou UniversityYangzhou 225009JiangsuChina Key Laboratory for Photonic and Electronic Bandgap Materials Ministry of EducationSchool of Physics and Electronic EngineeringHarbin Normal UniversityHarbin 150025HeilongjiangChina

Precisely refining the electronic structure of electrocatalysts represents a powerful approach to further optimize the electrocatalytic ***,we demonstrate an ingenious d-d orbital hybridization concept to construct Mo-doped Co_(9)S_(8) nanorod arrays aligned on carbon cloth(CC)substrate(abbreviated as Mo-Co_(9)S_(8)@CC hereafter)as a high-efficiency bifunctional electrocatalyst toward water *** has experimentally and theoretically validated that the 4d-3d orbital coupling between Mo dopant and Co site can effectively optimize the H_(2)O activation energy and lower H^(*)adsorption energy barrier,thereby leading to enhanced hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)*** to the unique electronic and geometrical advantages,the optimized Mo-Co_(9)S_(8)@CC with appropriate Mo content exhibits outstanding bifunctional performance in alkaline solution,with the overpotentials of 75 and 234 mV for the delivery of a current density of 10 mA cm^(-2),small Tafel slopes of 53.8 and 39.9 mV dec~(-1)and long-term stabilities for at least 32 and 30 h for HER and OER,*** impressively,a water splitting electrolylzer assembled by the self-supported Mo-Co_(9)S_(8)@CC electrode requires a low cell voltage of 1.53 V at 10 mA cm^(-2)and shows excellent stability and splendid reversibility,demonstrating a huge potential for affordable and scalable electrochemical H_(2) *** innovational orbital hybridization strategy for electronic regulation herein provides an inspirable avenue for developing progressive electrocatalysts toward new energy systems.

关键词： d-d orbital hybridization Transition metal sulfides Nanorods arrays Water electrolysis

N-doped hollow carbon nanospheres embedded in N-doped graphene forming a three-dimensional interconnected layered porous support loaded with palladium nanoparticles as an efficient electrocatalyst for formic acid oxidation

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新型炭材料(中英文) 2024年

作者： FANG Yue YANG Fu-kai QU Wei-li DENG Chao WANG Zhen-bo Key Laboratory of Photochemical Biomaterials and Energy Storage Materials Shenzhen Key Laboratory of Special Functional Materials Shenzhen Engineering Laboratory for Advance Technology of Ceramics Guangdong Research Center for Interfacial Engineering of Functional Materials College of Materials Science and Engineering Shenzhen University MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage School of Chemistry and Chemical Engineering State Key Lab of Urban Water Resource and Environment Harbin Institute of Technology college of chemistry and chemical engineering Harbin Normal University No.1 Normal University South Road

The efficient electrocatalysts with low cost, high activity and good durability plays a crucial role in the application of direct formic acid fuel cells. Herein, Pd nanoparticles supported on N-doped hollow carbon nanospheres (NHCN) embedded in Ndoped graphene (NG) with three-dimensional (3D) layered porous configuration by a simple and economical method were investigated as direct formic acid fuel cell catalysts. Owing to the unique 3D interconnected layered porous configuration doped with nitrogen atoms, Pd/NHCN@NG catalyst with smaller Pd nanoparticle size shows large catalytic active surface area, superior electrocatalyticactivity,highsteady-statecurrentdensity,strongabilitytoresistCOpoisoning,farsurpassingthoseofconventionalPd/C,Pd/NG,andPd/***/GOratio,itisfoundthatwhenthe HCN/GO mass ratio is 1∶1, Pd/NHCN@NG catalyst has the most outstanding performance in catalytic oxidation of formic acid,with an activity 4.21 times that of Pd/C. This work has developed a superior carbon-based support material for electrocatalysts, which brings broad application prospects for the development of fuel cells.

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Li-Rich Organosulfur Cathode with Boosted Kinetics for High-Energy Lithium-Sulfur Batteries

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Energy & Environmental Materials 2024年第4期7卷 118-125页

作者： Ting Ma Jiaojiao Deng Yuxiao Lin Qinghua Liang Liang Hu Xiaohu Wang Jun Liu Xinsheng Zhao Yinwei Li Ding Nan Xiaoliang Yu college of chemistry and chemical engineering Inner Mongolia University Inner Mongolia Key Laboratory of Graphite and Graphene for Energy Storage and Coating School of Materials Science and Engineering Inner Mongolia University of Technology Shenzhen Key Laboratory on Power Battery Safety and Shenzhen Geim Graphene Center Tsinghua Shenzhen International Graduate School (SIGS) school of Physics and Electronic engineering Jiangsu Normal University Key Laboratory of Rare Earth Ganjiang Innovation Academy Chinese Academy of Sciences Department of Mechanical engineering Research Institute for Smart EnergyThe Hong Kong Polytechnic University

Organosulfur materials containing sulfur-sulfur bonds are an emerging class of high-capacity cathodes for lithium ***,it remains a great challenge to achieve rapid conversion reaction kinetics at practical testing conditions of high cathode mass loading and low electrolyte *** this study,a Li-rich pyrolyzed polyacrylonitrile/selenium disulfide（pPAN/Se2S3） composite cathode is synthesized by deep lithiation to address the above challenges.

关键词： Electrolytes