超细WC粉末的强化球磨和表面钝化

研究了超细WC球磨破碎和分散机理,通过表面活性剂和聚合物的添加,降低了超细WC的球磨料浆粘度,提高了WC的球磨效率;经过150小时球磨后WC的BET小于100nm,X衍射晶粒度小于30nm。WC表面聚合物包覆的物理改性,其抗氧化能力提高了一倍。     

超高纯铁素体不锈钢在3．5％NaCl中的腐蚀疲劳的裂纹萌生

本文利用三电极技术研究了超高纯铁素体不锈钢Ｆｅ－２６Ｃｒ－１Ｍｏ在３．５％ＮａＣｌ水溶液转化体系中，低周腐蚀疲劳的裂纹萌生行为．在静态点蚀电位以下，形变诱发点蚀出现，但是点蚀在本文的研究体系不是导致裂纹萌生的原因．在低应变速率下，裂纹沿晶内的驻留滑移带萌生，且沿滑移带的电化学溶解加快了裂纹萌生．在高应变速率下，裂纹在晶界萌生，且沿晶界有点蚀实验结果表明，电化学溶解加速了裂纹萌生，点蚀在此钝化体系中不是裂纹萌生的机制．应变速率影响裂纹萌生方式．     

化学镀Ni-P合金在氯化物溶液中的化学钝化

本文对化学镀Ni-P合金在3.5%NaCl溶液中的阳极行为进行了研究。运用动电位极化技术和电化学阻抗谱(EIS)技术对活化区和钝化区的测量结果表明:过电位与呈线性关系,但不同电位区,其斜率相差较大。在活化区,界面电容C随过电位的增大而减小,而在钝化区,C维持恒定。对表面膜的XPS分析证实:在活化区形成有磷酸盐膜,保护性差,不能有效地抑制溶解过程;而当表面吸附有H2PO2阴离子时,合金进入化学致钝的钝化区.     

Development of flexible displays using back‐channel‐etched In–Sn–Zn–O thin‐film transistors and air‐stable inverted organic light‐emitting diodes

We developed flexible displays using back‐channel‐etched In–Sn–Zn–O (ITZO) thin‐film transistors (TFTs) and air‐stable inverted organic light‐emitting diodes (iOLEDs). The TFTs fabricated on a polyimide film exhibited high mobility (32.9 cm²/Vs) and stability by utilization of a solution‐processed organic passivation layer. ITZO was also used as an electron injection layer (EIL) in the iOLEDs instead of conventional air‐sensitive materials. The iOLED with ITZO as an EIL exhibited higher efficiency and a lower driving voltage than that of conventional iOLEDs. Our approach of the simultaneous formation of ITZO film as both of a channel layer in TFTs and of an EIL in iOLEDs offers simple fabrication process.     

Reliability and mechanical durability tests of flexible OLED with ALD coating

To improve the reliability and mechanical durability of a flexible organic light‐emitting diode display, the entire flexible display is coated with an aluminum oxide film by atomic layer deposition (ALD). Because the step coverage of ALD is excellent, the AlO_x film was deposited not only on the front and back surfaces but also on the side surfaces of the display. A high‐temperature and high‐humidity preservation test, repetitive bending tests, and a pencil hardness test were conducted on the flexible display with ALD‐AlO_x coating. The display survived 500 h of a 65°C, 95% preservation test, endured a 100,000‐time repetitive bending test with a curvature radius of 4 mm, and was found to have a pencil hardness of 4H.     

A Polymer Defect Passivator for Efficient Hole-Conductor-Free Printable Mesoscopic Perovskite Solar Cells

Due to the low cost and excellent potential for mass production, printable mesoscopic perovskite solar cells (p-MPSCs) have drawn a lot of attention among other device structures. However, the low open-circuit voltage (V_OC) of such devices restricts their power conversion efficiency (PCE). This limitation is brought by the high defect density at perovskite grain boundaries in the mesoporous scaffold, which results in severe nonradiative recombination and is detrimental to the V_OC. To improve the perovskite crystallization process, passivate the perovskite defects, and enhance the PCE, additive engineering is an effective way. Herein, a polymeric Lewis base polysuccinimide (PSI) is added to the perovskite precursor solution as an additive. It improves the perovskite crystallinity and its carbonyl groups strongly coordinate with Pb²⁺, which can effectively passivate defects. Additionally, compared with its monomer, succinimide (SI), PSI serves as a better defect passivator because the long-chained macromolecule can be firmly anchored on those defect sites and form a stronger interaction with perovskite grains. As a result, the champion device has a PCE of 18.84%, and the V_OC rises from 973 to 1030 mV. This study offers a new strategy for fabricating efficient p-MPSCs.     

基于锂电池的空间电源系统钝化研究

针对空间能源系统在卫星寿命末期的钝化需求,分析了不同轨道卫星锂电池的温度条件,同时分析了锂电池位置、卫星姿态对其温度的影响。基于上述分析的温度范围,研究了锂电池在钝化后发生热失控的可能性和影响因素,分析得到基于锂电池的空间电源系统钝化需求。在此基础上,提出了4种可行的钝化解决方案,并从受空间环境影响程度、额外增加元器件的情况以及钝化后电路受电流应力情况等方面进行对比,分析结果表明,旁路钝化方案是基于锂离子电池的电源系统钝化的首选方案。     

Passivating Defects of Perovskite Solar Cells with Functional Donor-Acceptor–Donor Type Hole Transporting Materials

In this study, a series of donor–acceptor–donor (D-A-D) type small molecules based on the fluorene and diphenylethenyl enamine units, which are distinguished by different acceptors, as holetransporting materials (HTMs) for perovskite solar cells is presented. The incorporation of the malononitrile acceptor units is found to be beneficial for not only carrier transportation but also defects passivation via Pb–N interactions. The highest power conversion efficiency of over 22% is achieved on cells based on V1359, which is higher than that of spiro-OMeTAD under identical conditions. This st shows that HTMs prepared via simplified synthetic routes are not only a low-cost alternative to spiro-OMeTAD but also outperform in efficiency and stability state-of-art materials obtained via expensive cross-coupling methods.     

All Inorganic Halide Perovskites Nanosystem: Synthesis,Structural Features,Optical Properties and Optoelectronic Applications

The recent success of organometallic halide perovskites (OHPs) in photovoltaic devices has triggered lots of corresponding research and many perovskite analogues have been developed to look for devices with comparable performance but better stability. Upon the preparation of all inorganic halide perovskite nanocrystals (IHP NCs), research activities have soared due to their better stability, ultrahigh photoluminescence quantum yield (PL QY), and composition dependent luminescence covering the whole visible region with narrow line‐width. They are expected to be promising materials for next generation lighting and display, and many other applications. Within two years, a lot of interesting results have been observed. Here, the synthesis of IHPs is reviewed, and their progresses in optoelectronic devices and optical applications, such as light‐emitting diodes (LEDs), photodetectors (PDs), solar cells (SCs), and lasing, is presented. Information and recent understanding of their crystal structures and morphology modulations are addressed. Finally, a brief outlook is given, highlighting the presently main problems and their possible solutions and future development directions.     

Differential Electrochemical Conductance Imaging at the Nanoscale

Electron transfer in proteins is essential in crucial biological processes. Although the fundamental aspects of biological electron transfer are well characterized, currently there are no experimental tools to determine the atomic‐scale electronic pathways in redox proteins, and thus to fully understand their outstanding efficiency and environmental adaptability. This knowledge is also required to design and optimize biomolecular electronic devices. In order to measure the local conductance of an electrode surface immersed in an electrolyte, this study builds upon the current–potential spectroscopic capacity of electrochemical scanning tunneling microscopy, by adding an alternating current modulation technique. With this setup, spatially resolved, differential electrochemical conductance images under bipotentiostatic control are recorded. Differential electrochemical conductance imaging allows visualizing the reversible oxidation of an iron electrode in borate buffer and individual azurin proteins immobilized on atomically flat gold surfaces. In particular, this method reveals submolecular regions with high conductance within the protein. The direct observation of nanoscale conduction pathways in redox proteins and complexes enables important advances in biochemistry and bionanotechnology.