气相输运沉积制备c轴择优取向的碘化铋薄膜

铋基卤化物材料因其无毒和优良的光电性能而显示出巨大的应用潜力。BiI₃作为一种层状重金属半导体,已被用于X射线检测、γ射线检测和压力传感器等领域,最近其作为一种薄膜太阳能电池吸收材料备受关注。本文采用简单的气相输运沉积(VTD)法,以BiI₃晶体粉末作为蒸发源,在玻璃基底上得到高质量c轴择优取向的BiI₃薄膜。并通过研究蒸发源温度和沉积距离对薄膜物相和形貌的影响,分析了BiI₃薄膜择优生长的机理。结果表明VTD法制备的BiI₃薄膜属于三斜晶系,其光学带隙为~1.8 eV。沉积温度对薄膜的择优取向有较大影响,在沉积温度低于270 ℃时,沉积的薄膜具有沿c轴择优取向生长的特点,超过此温度,c轴择优取向生长消失。在衬底温度为250 ℃、沉积距离为15 cm时制备的薄膜结晶性能最好,晶体形貌为片状八面体。     

对氯苯甲酸构筑的铜(Ⅱ)配合物的合成、HSA结合及细胞毒性

本文合成了配合物[Cu(pcba)₂·(phen)(H₂O)] (pcba =对氯苯甲酸,phen = 1,10-邻菲罗啉),该配合物属于三斜晶系,P1空间群,晶胞参数为a=0.790 98(2) nm,b=1.072 40(4) nm,c=1.487 19(6) nm,α=100.613(3)°,β=95.239(3)°,γ=108.334(3)°,Z=2,D_c=1.638 g·cm^-3,F(000)=582,最终结构残差因子R₁=0.035 9,wR₂=0.089 1。采用紫外及荧光研究了配合物和人血清蛋白(HSA)的相互作用方式。结果表明,配合物静态猝灭HSA荧光,可求得配合物与HSA的猝灭常数K_sv=2.35×10⁵ L·mol^-1,猝灭速率常数K_q=2.35×10¹³ L·mol^-1·s^-1,结合常数为K_a=2.14×10¹³ L·mol^-1,结合位点n=2.37。同时,研究了配合物对胃癌细胞A549、宫颈癌细胞Hela和肝癌细胞HepG2的抗增殖能力。     

自掺杂SnO2微球的水热合成及其可见光催化性能

本研究采用水热法,以柠檬酸为螯合剂,通过控制n(Sn⁴⁺)/n(Sn²⁺)的数值,合成了由具有丰富氧空位的SnO₂纳米晶体组装成的微球。通过X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、傅里叶红外光谱(FT-IR)、X射线光电子能谱(XPS)及UV-Vis漫反射光谱对SnO₂纳米微球进行表征分析,结果表明:在酸性水热条件和柠檬酸的螯合作用下,二氧化锡纳米晶体聚集形成微球;在Sn⁴⁺/Sn²⁺摩尔比例为3:7时,其微球尺寸最小,整体分散性较好;同时适量二价锡离子的掺杂使得该样品氧空位浓度达到最佳,氧空位的存在将使得样品光吸收范围拓展至可见光,因而该样品显示出较强的可见光催化效率,在8 min内完全降解甲基橙。     

基于PI法的门源MS6.4地震前震中附近地震热点图像异常变化研究

基于1980年以来青海省和甘肃省区域地震台网的定位地震目录，分析了研究区最小完备震级，选取空间网格尺度为0.2°×0.2°、地震活动异常学习时间段和预测时间段均为3 a，应用图像信息（PI）法，分析了门源M_S6.4地震发生前震中附近地震热点图像的异常变化过程。结果表明，在2013年1月1日至2016年1月1日的预测时间窗内，冷龙岭断裂和祁连山北缘断裂附近存在明显的地震热点，且地震热点图像颜色偏深，发震概率较高，向前滑动至2014年1月1日至2017年1月1日，2015年1月1日至2018年1月1日和2016年1月1日至2019年1月1日3个预测时间窗，此两断裂附近仍存在地震热点，地震热点图像颜色逐渐由深变浅，而门源M_S6.4地震就落在PI法得到的地震热点内。门源M_S6.4地震前存在明显的地震热点，且地震热点相对集中，地震热点图像颜色由深变浅，震后消失；在祁连山北缘断裂附近，地震热点持续存在，分布较集中，地震热点图像颜色也呈由深变浅的过程。未来需关注祁连山北缘断裂，附近有发生强震的可能。     

以含碘氨基酸类激素为例刍议微量非金属元素在生物体内的作用机制

选取第五周期元素碘,结合多学科的研究方法论对含碘氨基酸类激素在生物体内的合成和分解代谢进行系统性分析。通过解析碘元素本身性质及其各个氧化态之间的转化,探讨碘元素在生物体内的作用机制,揭示自然界对物质代谢的精细调控。这一教学模式探索性地融入无机化学、元素有机化学、分子生物学、生物化学、生物物理学、化学生物学等一系列学科内容,旨在让学生在领悟生命科学内在规律,从而激发其科研及学习热情,并训练学生的类比思维和思辨能力。期对培养21世纪跨学科综合型人才的培养有所助益。     

Effect of Support on Catalytic Performance of Photothermal Fischer-Tropsch Synthesis to Produce Lower Olefins over Fe5C2-based Catalysts

Photothermal Fischer-Tropsch synthesis(FTS) has been extensively studied, but few reports were focused on systematically exploring the influence of support on catalytic performance. Herein, a series of Fe₅C₂-based catalysts with different supports was fabricated via a one-step wet-chemical method for photothermal conversion of syngas to lower olefins. Under light irradiation, the optimized Fe₅C₂/α-Al₂O₃ catalyst demonstrated remarkable photothermal FTS activity, delivering selectivity to lower olefins of 50.3% with a CO conversion rate of 52.5%. Characterization studies using X-ray diffraction and Mössbauer spectroscopy analysis revealed that the active catalyst mainly contained Fe₅C₂ nanoparticles on α-Al₂O₃ support. It was found that the weak interaction between active phase and α-Al₂O₃ could promote the formation of Fe₅C₂, which contributed to the high selectivity to lower olefins.     

Nanostructured BiVO4 Derived from Bi-MOF for Enhanced Visible-light Photodegradation

BiVO4,a promising visible-light responding photocatalyst,has aroused extensive research interest because of inexpensiveness and excellent chemical stability.However,its main drawback is the poor photoinduced charge-transfer dynamics.Building nanostructures is an effective way to tackle this problem.Herein,we put forward a new method to prepare nanostructured BiVO4 from Bi-based metal-organic frameworks[Bi-MOF(CAU-17)]precursor.The as-prepared material has a rod-like morphology inherited from the Bi-MOF sacrificial template and consists of small nanoparticle as building blocks.Compared with its counterparts prepared by conventional methods,MOF-derived nanostructured BiVO4 shows better light absorption ability,narrower bandgap,and improved electrical conductivity as well as reduced recombination.Consequently,BiVO4 nanostructure demonstrates high photocatalytic activity under visible light towards the degradation of methylene blue.Methylene blue can be degraded up to 90%within 30 min with a reaction rate constant of 0.058 min-1.Moreover,the cycling stability of the catalyst is excellent to withstand unchanged degradation efficiency for at least 5 cycles.     

侧向点爆炸作用下地下拱结构的动力响应

首先，利用几何关系与介质中超压、位移衰减公式得出结构表面自由场荷载和位移的分布形式，并对衰减因数、爆距等参数进行讨论；其次，利用MSSI（modified soil-structure interaction）相互作用模型对拱的振动方程进行正交求解，得到任意角度荷载作用下的结构弹性动力响应解析解。基于动力响应解析解，得到了土体的声阻抗对结构位移、速度、加速度时程响应曲线的影响。研究结果表明:侧向爆炸荷载作用下，岩土介质声阻抗越大，埋设其中的地下结构的位移、速度和加速度变化越大。为此，建议地下防护结构应修建在声阻抗小的岩土介质中。     

三维复杂流动的间断有限元方法模拟

本文基于三维可压缩Euler方程,采用基于Runge-Kutta时间离散的间断有限元方法(RKDG方法),对三维前台阶、三维Riemann问题和球Riemann等问题进行了模拟。结果表明,本文的RKDG方法能够在很少的网格内清晰地捕捉到三维复杂流场中的激波和接触间断;同时,将球Riemann问题中z=0.4平面压强沿到对称轴距离的分布与文献中的近似精确解相比,吻合较好,这也验证了本文的RKDG方法不仅能够进行三维复杂流场的定性描述,也能够应用于三维复杂流场的定量计算。     

常压微等离子体阳极与离子溶液界面的电荷转移反应

Atmospheric- pressure microplasma is an attractive gaseous electrode, and may replace the commonly used rare metal electrodes for electrochemical reactions. The reactions at the plasma anode-liquid interface have not been well investigated, and application of plasma anodes to electrodeposition is still rare. In this communication, by choosing the oxidation of ferrocyanide to ferricyanide as a model reaction, we carefully investigated the charge-transfer reaction at the interface between a plasma anode and an ionic solution. The results showed that ferrocyanide was progressively oxidated to ferricyanide over time, and the rate of oxidation was proportional to the discharge current. We also found that after the discharge the oxidation percent of ferrocyanide still increased approximately linearly with storage time, and the increasing rate was dependent on the discharge time. The rate of oxidation after discharge was much lower than that caused by discharge. These results demonstrate that atmospheric-pressure microplasma could act as a gaseous anode for transferring positive charges at the plasma-liquid interface and inducing electrochemical reactions in solution. During discharge, oxidative active species were also produced. We also successfully electrodeposited copper on stainless steel with the assistance of a microplasma anode in CuSO4 saturated solution, and the current efficiency was about 90%.