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In-situ topotactic construction of novel rod-like Bi_(2)S_(3)/Bi_(5)O_(7)I p-n heterojunctions with highly enhanced photocatalytic activities
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作者 Peng Ju Lei Hao +6 位作者 Yu Zhang Jianchao Sun Kunpeng Dou Zhaoxia Lu Dankui Liao Xiaofan Zhai Chengjun Sun 《Journal of Materials Science & Technology》 SCIE EI CAS CSCD 2023年第4期126-141,共16页
In this work,a novel Bi_(2)S_(3)/Bi_(5)O_(7)I p-n heterojunction with three-dimensional rod-like nanostructure was successfully constructed through an in-situ topotactic ion exchange approach.A possible evolution mech... In this work,a novel Bi_(2)S_(3)/Bi_(5)O_(7)I p-n heterojunction with three-dimensional rod-like nanostructure was successfully constructed through an in-situ topotactic ion exchange approach.A possible evolution mech-anism from Bi_(5)O_(7)I nanobelts(NBs)into Bi_(2)S_(3)/Bi_(5)O_(7)I rod-like heterostructures(BSI RHs)was proposed,depicting the self-assembly process of internal Bi_(5)O_(7)I NBs and outside networks interwoven by Bi_(2)S_(3)nanorods(NRs),which abided by the Ostwald ripening and epitaxial growth.Owing to the formation of p-n heterojunction and rich oxygen vacancies(OVs),the visible-light absorption ability and separation of photogenerated charge carriers of BSI RHs were highly promoted,leading to a greatly improved photocatalytic ability than that of Bi_(2)S_(3)and Bi_(5)O_(7)I.BSI-1 exhibited the strongest photocatalytic performance,and almost all rhodamine B(RhB)and Pseudomonas aeruginosa(P.aeruginosa)can be thoroughly removed within 90 min.Moreover,a possible photocatalytic mechanism of BSI RHs was proposed based on the tests of active species trapping,electron spin resonance(ESR),photoelectrochemistry(PEC),and photoluminescence(PL)combined with the density functional theory(DFT)simulated computation,vali-dating the dominating roles of·O_(2)^(−)and h+during the photocatalytic process.This work is expected to motivate further efforts for developing novel heterostructures with highly efficient photocatalytic performances,which presents a promising application prospect in the fields of energy and environment. 展开更多
关键词 ANTIfoULING Bi_(5)o_(7) I Photocatalytic HETERosTRUCTURE Bi_(2)s_(3)
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NSO-X(X=Cl,F)晶体双折射性质的第一性原理研究
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作者 张翡 杨辉 《四川大学学报(自然科学版)》 CAS CSCD 北大核心 2023年第5期179-183,共5页
为了拓宽双折射晶体的探索范围,更为便捷地探索新型的双折射晶体,本文根据阴离子基团理论,参考了硼酸盐等性能优异的双折射晶体结构,从众多晶体中选择了结构类似、含有平面π共轭电子体系的N_(3)PS_(2)O_(2)Cl_(4)晶体和CN_(5)S_(5)O_(... 为了拓宽双折射晶体的探索范围,更为便捷地探索新型的双折射晶体,本文根据阴离子基团理论,参考了硼酸盐等性能优异的双折射晶体结构,从众多晶体中选择了结构类似、含有平面π共轭电子体系的N_(3)PS_(2)O_(2)Cl_(4)晶体和CN_(5)S_(5)O_(3)F晶体,对其晶体结构进行分析.其中N_(3)PS_(2)O_(2)Cl_(4)晶体主体部分为N_(3)PS_(2)六元环,而S_(4)N_(4)八元环为CN_(5)S_(5)O_(3)F晶体提供了共轭π键.本文采用基于密度泛函理论的第一性原理计算,研究了其能带、态密度及双折射率等性质,结果表明,两种晶体在特定波段的双折射率大于0.1,存在成为优异双折射晶体的可能,其中CN_(5)S_(5)O_(3)F晶体由于优异的各向异性使得其双折射性质更为突出.本文在不进行大量艰难的晶体生长实验的条件下,评估这两晶体是否适合作为双折射晶体,提供了一种根据晶体结构探索新型双折射晶体的便捷方法. 展开更多
关键词 双折射晶体 第一性原理 密度泛函理论 N_(3)Ps_(2)o_(2)Cl_(4) cn_(5)s_(5)o_(3)f 共轭π键
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黄金湿法冶炼含氰废水深度处理工艺比选 被引量:1
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作者 刘锐利 赵次娴 +6 位作者 戴镇璇 雷吟春 孟云 谭琴 廖圆 齐伟 王凯 《广东化工》 CAS 2024年第4期107-110,共4页
针对某黄金冶炼公司冶炼厂含氰废水,采用Na_(2)SO_(3)/空气法、Na_(2)S_(2)O_(5)/空气法、H_(2)O_(2)氧化法、NaClO氧化法四种工艺进行深度净化。试验确定Na_(2)SO_(3)/空气法处理的最佳工艺参数为:反应p H=9、反应时间25 min、Na_(2)SO... 针对某黄金冶炼公司冶炼厂含氰废水,采用Na_(2)SO_(3)/空气法、Na_(2)S_(2)O_(5)/空气法、H_(2)O_(2)氧化法、NaClO氧化法四种工艺进行深度净化。试验确定Na_(2)SO_(3)/空气法处理的最佳工艺参数为:反应p H=9、反应时间25 min、Na_(2)SO_(3)药剂用量0.1 g/L;Na_(2)S_(2)O_(5)/空气法处理的最佳工艺参数为:反应pH=10、反应时间30 min、Na_(2)S_(2)O_(5)药剂用量0.1 g/L;H_(2)O_(2)氧化法处理,H_(2)O_(2)药剂用量0.15 g/L;NaClO氧化法处理,NaClO药剂用量0.2 g/L。通过对比分析以上4种处理工艺的成本及优缺点,确定最佳处理工艺。本研究为含氰废水深度处理提供了技术支持。 展开更多
关键词 含氰废水 Na_(2)so_(3)/空气法 Na_(2)s_(2)o_(5)/空气法 H_(2)o_(2)氧化法 氯碱氧化法
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造孔剂法制备泡沫铁及其性能研究
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作者 张驰 黄尧 +1 位作者 王芳 黄闻战 《铸造设备与工艺》 2024年第2期28-32,共5页
本文选择了一种新型造孔剂Na_(2)S_(2)O_(3)·5H_(2)O(五水硫代硫酸钠),用该造孔剂制备出了孔径分别为2mm、3mm和4mm,孔隙率60%和70%的泡沫铁;并对孔径为2mm、3mm和4mm以及孔隙率为60%和70%的泡沫铁进行了力学性能与吸能性试验。结... 本文选择了一种新型造孔剂Na_(2)S_(2)O_(3)·5H_(2)O(五水硫代硫酸钠),用该造孔剂制备出了孔径分别为2mm、3mm和4mm,孔隙率60%和70%的泡沫铁;并对孔径为2mm、3mm和4mm以及孔隙率为60%和70%的泡沫铁进行了力学性能与吸能性试验。结果表明,用新型造孔剂Na_(2)S_(2)O_(3)·5H_(2)O制备的泡沫铁,结构可控;孔径、孔隙率和烧结温度都对泡沫铁的性能有不同程度的影响,在本试验参数下孔径为2 mm,孔隙率为60%,烧结温度为1150℃时,具有最佳的吸能性能和力学性能。 展开更多
关键词 泡沫铁 占位剂法 Na_(2)s_(2)o_(35H_(2)o 力学性能
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Ferrielectricity in DyMn_(2)O_(5):A golden touchstone for multiferroicity of RMn_(2)O_(5) family
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作者 J.-M.Liu S.Dong 《Journal of Advanced Dielectrics》 CAS 2015年第2期29-46,共18页
The RMn_(2)O_(5) manganite compounds represent one class of multiferroic family with magnetic origins,which has been receiving continuous attention in the past decade.So far,our understanding of the magnetic origins f... The RMn_(2)O_(5) manganite compounds represent one class of multiferroic family with magnetic origins,which has been receiving continuous attention in the past decade.So far,our understanding of the magnetic origins for ferroelectricity in RMn_(2)O_(5) is associated with the nearly collinear antiferromagnetic structure of Mn ions,while the exchange striction induced ionic displacements are the consequence of the spin frustration competitions.While this scenario may be applied to almost all RMn_(2)O_(5) members,its limitation is either clear:the temperature-dependent behaviors of electric polarization and its responses to external stimuli are seriously materials dependent.These inconsistences raise substantial concern with the state-of-the-art physics of ferroelectricity in RMn_(2)O_(5).In this mini-review,we present our recent experimental results on the roles of the 4f moments from R ions which are intimately coupled with the 3d moments from Mn ions.DyMn_(2)O_(5) is a golden figure for illustrating these roles.It is demonstrated that the spin structure accommodates two nearly collinear sublattices which generate respectively two ferroelectric(FE)sublattices,enabling DyMn_(2)O_(5) an emergent ferrielectric(FIE)system rarely identified in magnetically induced FEs.The evidence is presented from several aspects,including FIE-like phenomena and magnetoelectric responses,proposed structural model,and experimental check by nonmagnetic substitutions of the 3d and 4f moments.Additional perspectives regarding possible challenges in understanding the multiferroicity of RMn_(2)O_(5) as a generalized scenario are discussed. 展开更多
关键词 RMn_(2)o_(5) MULTIfERRoIC ferrielectricity 3d-4f coupling exchange striction.
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高磷赤铁矿直接还原过程中CaO脱磷机制的分子动力学模拟 被引量:1
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作者 李宗蔚 寇珏 +1 位作者 孙体昌 陈泽坤 《有色金属(选矿部分)》 CAS 北大核心 2022年第6期35-42,84,共9页
利用分子动力学模型(MD)模拟了在焙烧过程中(1150℃)不同用量CaO加入到Fe_(2)O_(3)-Ca_(5)(PO_(4))_(3)F-SiO_(2)三元体系后微观结构的变化规律,并借此阐明高磷赤铁矿直接还原过程中CaO的脱磷机制。分子动力学模拟和拉曼光谱分析结果表... 利用分子动力学模型(MD)模拟了在焙烧过程中(1150℃)不同用量CaO加入到Fe_(2)O_(3)-Ca_(5)(PO_(4))_(3)F-SiO_(2)三元体系后微观结构的变化规律,并借此阐明高磷赤铁矿直接还原过程中CaO的脱磷机制。分子动力学模拟和拉曼光谱分析结果表明,四元体系中的Si和P会形成四面体结构,体系中的非桥氧占主导地位。随着CaO添加量的增加,体系中Ca_(5)(PO_(4))_(3)结构更加稳定。体系中Si—O—Si为主的桥氧含量减少,复杂的[SiO_(4)]四面体减少,Si—O聚合体的聚集度降低。阐明了直接还原过程中CaO是通过解聚[SiO_(4)]四面体结构,减少了SiO_(2)与磷灰石的接触,从而抑制磷灰石还原达到脱磷效果的。 展开更多
关键词 fe_(2)o_(3)-Ca_(5)(Po_(4))_(3)f-sio_(2)体系 分子动力学模拟 直接还原 高磷赤铁矿
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