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结构化学
结构化学

吴新涛

月刊

0254-5861

jghx@fjirsm.ac.cn

0591-83704886,83704896

350002

福建省福州市杨桥西路155号

结构化学/Journal Chinese Journal of Structural ChemistryCSCD北大核心CSTPCDSCI
查看更多>>本刊是中国科学院主管,中国化学会、中国科学院福建物质结构研究所主办的学术性期刊。2006年改为纯英文版“Chinese Journal of Structural Chiemistry”。主要报道晶体学,量子化学,药物、材料和催化剂等领域物质性能与结构关系的文章。报道的内容涉及有机化学、无机化学、合成化学、结构化学、材料科学、药物化学、晶体学、理论化学等学科中的微观物质结构与性能关系的研究成果或阶段性成果。与此同时本刊也报道用谱学等物理方法解析物质结构、阐述物质结构与性能关系的论文。《结构化学》是中国自然科学核心期刊,中国科技论文引文数据库来源及统计源期刊。
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    S-scheme heterojunction photocatalyst for H2 evolution coupled with organic oxidation

    Bicheng ZhuJingsan Xu
    1-2页

    Reconstruction mechanism of Cu surface in CO2 reduction process

    Ping WangTianbao ZhangZhenxing Li
    3-4页

    PVDF-based solid-state battery

    Biao FangRunwei Mo
    5-7页

    Modulation of dinuclear site by orbital coupling to boost catalytic performance

    Jian JiJie YanHonggen Peng
    8-9页

    Ni-based electrocatalysts for urea-assisted water splitting

    Shuyuan PanZehui YangFang Luo
    10-11页

    Water reduction by an organic single-chromophore photocatalyst

    Kun TangYu-Wu Zhong
    12-14页

    Mesoporous CuCe dual-metal catalysts for efficient electrochemical reduction of CO2 to methane

    Tinghui YangMin KuangJianping Yang
    15-17页

    Modulating pollutant adsorption and peroxymonosulfate activation sites on Co3O4@N,O doped-carbon shell for boosting catalytic degradation activity

    Ruiying LiuLi ZhaoBaishan LiuJiayuan Yu...
    18-26页
    查看更多>>摘要:The construction of double active sites for pollutant adsorption and peroxymonosulfate(PMS)activation on the surface of catalyst is conducive to further enhancing the pollutant-removing effect.Herein,a N,O co-doped carbon-encapsulated tricobalt tetraoxide(Co3O4@N,O-C)with double active sites is prepared by a one-step laser carbonization method.The optimized Co3O4@N,O-C shows excellent tetracycline(TC)removal ability,in which the k value reaches 0.608 min-1.On the surface of Co3O4@N,O-C,TC is adsorbed to the N site,and PMS is activated at the O site.Building double active sites on the catalyst surface not only avoids competition for the active site,but also confines the pollutant molecules to the surface of the catalyst,thus shortening the migration distance between reactive oxygen species(ROS)and the pollutant and boosting the removal efficiency of pol-lutants.In addition,the Co3O4@N,O-C/PMS system exhibits both good resistance to environmental interference and cyclic stability.Finally,a practical continuous flow reactor based on Co3O4@N,O-C catalyst is built,which shows a stable and efficient TC degradation performance.

    Deciphering the structural evolution and real active ingredients of iron oxides in photocatalytic CO2 hydrogenation

    Mengjun ZhaoYuhao GuoNa LiTingjiang Yan...
    27-37页
    查看更多>>摘要:Photocatalytic CO2 hydrogenation reactions can produce high-value-added chemicals for industry,solving the environmental problems caused by excessive CO2 emissions.Iron oxides are commonly used in photocatalytic reactions due to their various structures and suitable band gaps.Nevertheless,the structural evolution and real active components during photocatalytic CO2 hydrogenation reaction are rarely studied.Herein,a variety of iron oxides including a-Fe2O3,y-Fe2O3,Fe3O4 and FeO were derived from Prussian blue precursors to investigate the CO2 hydrogenation performance,structural evolution and active components.Especially,the typical a-andγ-Fe2O3 are converted to Fe3O4 during the reaction,while Fe/FexOy remains structurally stable.Meanwhile,it is confirmed that Fe3O4 is the main active component for CO production and the formation of hydrocarbons(CH4 and C2-C4)are highly dependent on the Fe/FexOy heterojunctions.The optimal yields of CO,CH4 and C2-C4 hydrocarbons over the best catalyst(FeFe-550)can achieve 4 mmol g-1 h-1,350 μmol g-1 h-1 and 150 μmol g-1 h-1,respectively due to their suitable metal/oxide component distribution.This work examines the structural evolution of different iron oxide catalysts in the photocatalytic CO2 hydrogenation reaction,identifies the active components as well as reveals the relationship between components and the products,and offers valuable insights into the efficient utilization of CO2.

    All in one doubly pillared MXene membrane for excellent oil/water separation,pollutant removal,and anti-fouling performance

    Changle LiuMingyuzhi SunHaoran ZhangXiqian Cao...
    38-47页
    查看更多>>摘要:Given the diversity and complexity of coexisting oil/dyes/heavy metal ions/microorganisms in wastewater and volatile organic compounds(VOCs)in the air,developing separation materials featured in higher separation efficiency and lower energy consumption for oil and water separation,pollutant removal,and anti-fouling is urgently needed,but it remains a major challenge till now.Herein,a multifunctional Ti3C2 MXene membrane with unique double pillar support was proposed by liquid phase ultrasonication and vacuum filtration to over-come the above challenge.Introducing cetyl-trimethyl ammonium bromide(CTAB)and calcium chloride/sodium alginate(CaCl2/SA)to the MXene membrane as crossed double pillars and superhydrophilic surface increases the tolerance and wettability of the membrane.The fabricated doubly pillared MXene(d-Ti3C2)membrane exhibits superior oil/water(O/W)separation efficiency(99.76%)with flux(1.284 L m-2 h-1)for canola oil and organic dye removing efficiency for methyl blue(MB)99.85%,malachite green(MG)100%,and methyl violet(MV)99.72%,respectively,which is 1.05,1.44,1.22,and 1.28 fold compared with pre-pillared Ti3C2(p-Ti3C2).The superior anti-oil/dye/fouling is attributed to lower oil conglutination,high hydrophily,and antibacterial activity.The versatile MXene membrane also shows distinguished separation of VOCs(η>99%)from polluted air.The experimental and molecular dynamics(MD)computational simulation results illustrate that the superior sepa-ration efficiency of the Ti3C2 MXene membrane is ascribed to the unique doubly pillared space channel.This study paves a new road to further research on one step integration strategy for complex O/W separation,wastewater and VOCs removal,and anti-fouling via tuning nano/macro architecture.