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    Research Progress of MOF-SACs in Water Splitting for Hydrogen Evolution Reaction
    HE Yutong, LI Hanxi, FAN Xiaoyan, YU Meihui, ZHANG Jijie
    Chem. J. Chinese Universities    2026, 47 (3): 20250333-.   DOI: 10.7503/cjcu20250333
    Abstract543)   HTML46)    PDF(pc) (10493KB)(30663)       Save

    The hydrogen evolution reaction(HER) from photocatalytic and electrocatalytic water splitting is a pivotal technology of future green hydrogen economy, but the synthesis of low cost, high efficiency catalysts with high stability remains a critical scientific challenge to be addressed for both. Single-atom catalysts(SACs) are regarded as one of the most promising catalysts due to their unique electronic structure and maximum atomic utilization. The metal-organic framework materials(MOFs) are ideal single atoms carriers due to ultra-high specific surface area, tunable porous nanostructure, and abundant active sites, serving as SACs synthesis precursors owing to their unique pyrolysis characteristics. The composite system of MOFs and single atom catalysts(MOF-SACs) can take full advantage of the synergistic effect, thus improving the hydrogen evolution catalytic activity significantly. In this review, the recent applications and research progress of MOF-SACs in photocatalytic and electrocatalytic water splitting for hydrogen production progress are introduced, while the strategies for enhancing the catalytic activity are summarized. Moreover, the future research hotspots and trends are outlined, which can provide novel design models for HER catalysts.

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    Ion-transfer Reaction of SO42- Across the Water/1,2-dichloroethane Interface Modified by an Anion Exchange Membrane
    WANG Huanhuan, HU Daopan, JIANG Xuheng, ZHANG Yehua, CHEN Yong
    Chem. J. Chinese Universities    2016, 37 (3): 546-551.   DOI: 10.7503/cjcu20150626
    Abstract2755)   HTML174)    PDF(pc) (1546KB)(25702)       Save

    In this work, the anion-transfer reaction of highly hydrophilic sulfate across the water/1,2-dichloroethane(W/DCE) interface modified by a homogeneous anion exchange membrane(AEM) was investigated by employing cyclic voltammetry(CV), differential pulse voltammetry(DPV) and chronocoulometry. It was found that the electrochemical window could be extended by the modification of W/DCE interface with such an AEM. In addition, the well-defined CV and DPV curves corresponding to the ion-transfer of highly hydrophilic SO42- could be obtained at the modified W/DCE interface. According to the linear relationship between the peak current of CV and the square root of scan rate, as well as the equation of Randles-Sevik, the diffusion coefficient of SO42- in the membrane containing water is calculated to be about 7.6×10-8 cm2/s. In addition, the peak current of DPV increases linearly with the concentration of SO42-within the range of 5-25 mmol/L. Moreover, the standard reaction rate constant of the ion-transfer of SO42- at such an AEM-modified W/DCE interface was estimated to be about 1.49×10-3 cm/s via chronocoulometry.

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    Colloidal Lithography——Construction and Application of Nanostructured Surfaces
    ZHANG Gang*, ZHAO Zhi-Yuan, WANG Da-Yang
    Chem. J. Chinese Universities    2010, 31 (5): 839-854.  
    Abstract4421)      PDF(pc) (11337KB)(12353)       Save

    Combining “top-down” patterning with “bottom-up” self-assembly as template colloidal lithography provides a unique patterning strategy. Spontaneous formation of well-ordered colloidal arrays provides lithographic masks or scaffolds for creating useful patterns. Based on self-assembly of colloidal spheres as template, the controlled “positive” deposition of nanoparticles and “negative” etching processes could be used for the fabrication of nanostructured materials, ranging from several tens of nanometers to micrometer scales for 2D and 3D ordered architectures. The feature size can easily shrink below 100 nm by reducing the diameter of the microspheres used according to the simple correlation between the interstice size and the sphere diameter. The feature shape can be easily diversified by the crystalline structure of a colloidal crystal mask, the time of anisotropic etching of the mask, the incidence angle of the vapor beam and the mask registry. Colloidal lithography provides a complementary tool for conventional and fully “top-down” lithographic techniques, and thus holds immense promise in surface patterning. They show versatility applications such as biosensors or chemosensors using for detection tool. Colloidal lithography is also suitable for modifying surface properties which is useful for emerging applications in biotechnology and chemically and structurally designed interactive sites for the attachment.

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    Cover and Content of Chemical Journal of Chinese Universities Vol.34 No.9(2013)
    Chem. J. Chinese Universities    2013, 34 (9): 0-0.  
    Abstract1635)      PDF(pc) (16292KB)(8908)       Save
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    Self-Assembly Ultrathin Films Based On Dendrimers
    WANG Jin-Feng, JIA Xin-Ru, LI Ying, ZHONG Hong, CHEN Jin-Yu, LUO Guo-Bin, LI Ming-Qian, WEI Yen
    Chem. J. Chinese Universities    2001, 22 (10): 1773-1775.  
    Abstract1631)      PDF(pc) (1079KB)(7363)       Save
    An ultrathin film with forth generation poly(aminoamine)(PAMAM) dendrimers (methyl quaternary ammonium salt) as polycation and poly(sodium p styrenesulfonate) (PSS) as polyainon was fabricated via sequential deposition. It shows that the step by step depositions carried out smoothly by monitoring with UV Vis spectrometer. The multilayer film is rather flat with a mean roughness of 0.39 nm determined by AFM. The average thickness of a bilayer is 5.0 nm obtained from XRD, which indicates that the dendrimers molecules were compressed and possess high flattening.
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    Cover and Content of Chemical Journal of Chinese Universities Vol.34 No.2(2013)
    Chem. J. Chinese Universities    2013, 34 (2): 0-0.  
    Abstract1733)      PDF(pc) (14662KB)(7276)       Save
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    Cl- Mediated Facet Engineering and Electronic Modulation of Fe/MgO-CaO Catalysts for Glycerol Hydrogenolysis
    MU Rongzhen, WANG Jin, YANG Jie, ROY Tania, WANG Jie, GUO Baocheng, ZHOU Chunhui
    Chem. J. Chinese Universities    2026, 47 (8): 20250394-.   DOI: 10.7503/cjcu20250394
    Abstract121)   HTML3)    PDF(pc) (7100KB)(6903)       Save

    To overcome the limitations of active component aggregation and uncontrolled facet exposure typical of impregnation methods, we report a chloride-mediated engineering strategy to precisely tailor the morphology and electronic structure of Fe/MgO-CaO catalysts. Structural characterizations reveal that the gas-etching effect during NH₄Cl pyrolysis creates a porous architecture. Acting as a morphological modifier, NH₄Cl induces the directional growth of MgO-CaO from disordered sheets into a rod-like structure with preferentially exposed(200) facets. At the microstructural level, Cl⁻ doping strengthens the interaction between Fe species and the MgO lattice. This effectively inhibits the agglomeration of active components and promotes the formation of a highly dispersed Mg-Fe-O solid solution, while generating uniformly distributed Lewis acid sites on the catalyst surface. Consequently, the unique rod-like solid solution exhibits excellent structural stability during the catalytic reaction, successfully preventing framework collapse. Consequently, the optimized catalyst(Fe-Cl=1.00) boosted glycerol conversion from 60% to 90% relative to the Cl- free benchmark. This chloride-mediated engineering strategy provides a blueprint for valorizing natural minerals and rationally designing robust non-noble metal catalysts.

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    Highly Selective Detection of Fe3+ by Mononuclear Cd(II) Complex Sensor Containing Naphthalene Disulfonic Acid Ligands
    SONG Zhiguo, WANG Xin, ZHU Zhihui, XU Yiminmg, WANG Min
    Chem. J. Chinese Universities    2026, 47 (8): 20260062-.   DOI: 10.7503/cjcu20260062
    Abstract93)   HTML3)    PDF(pc) (9334KB)(6751)       Save

    A new type of stable fluorescent cadmium complex, Cd(C3H4N24(C10H6O6S22[abbreviated as Cd(Im)4(1,5-NDA)2], was synthesized by solvothermal method using cadmium nitrate tetrahydrate as the metal source, 1,5-naphthalenedisulfonate(1,5-NDA2-) and iImidazole(Im) as the main and auxiliary ligands. The compound was characterized by X-ray single crystal diffraction and thermogravimetric analysis. The X-ray single crystal diffraction results indicated that the compound belonged to the Monoclinic crystal system with the C1c1 space group, and the central ion Cd(II) was located in the distorted octahedral structure. The thermogravimetric analysis results proved that the compound had good thermal stability. The fluorescence properties of Cd(Im)4(1,5-NDA)2 were investigated. The solid-state fluorescence spectra showed that the compound had good fluorescence properties, and its fluorescence emission mainly came from the π-π* transition of the ligands. The orbital contributions of the excited state of the complex were calculated using the time-dependent density functional theory(TD-DFT). The fluorescence quenching experiments results indicated that Fe3+ had a significant quenching effect on the fluorescence intensity of the complex, and the detection limit of Fe3+ recognition by the complex was 0.46 μmol/L. By using the multi-technology combined approach, the possible fluorescence quenching mechanism of Fe3+ on Cd(Im)4(1,5-NDA)2 was speculated. The results of ultraviolet-visible absorption tests indicated that energy resonance transfer(FRET) occurred between Fe3+ and Cd(Im)4(1,5-NDA)2. The characterization results of powder X-ray diffraction, infrared spectroscopy, inductively coupled plasma mass spectrometry, energy dispersive spectroscopy and X-ray photoelectron spectroscopy showed that there were interactions between Fe3+ and N atoms on Cd(Im)4(1,5-NDA)2. In summary, the fluorescence quenching mechanism of Fe3+ on Cd(Im)4(1,5-NDA)2 is a dual-path cooperative quenching: FRET between Fe3+ and the complex and the interactions between Fe3+ and the N atoms on the complex.

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    Research Progress on the Synthesis of Pillar[n]arenes and Their Host-guest Chemistry
    WANG Kai, YANG Ying-Wei, ZHANG Sean Xiao-An
    Chem. J. Chinese Universities    2012, 33 (01): 1-13.   DOI: 10.3969/j.issn.0251-0790.2012.01.001
    Abstract8351)      PDF(pc) (951KB)(5882)       Save
    Pillararenes are a new class of host molecules, which are cyclic oligomers consisting of hydroquinones or 1,4-disubstituted hydroquinone ethers linked by methylene bridges in the para positions of the benze rings. Herein, recent development on the synthesis of pillar[n]arenes and pillar[n]arene derivatives, and their host-guest chemistry, i.e., molecular recognition and selective binding towards guest molecules, and their self-assembly properties was reviewed. In addition, prospects for future research based on pillar[n]arenes were also discussed.
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    Molecular Stacking and Device Performance: Recent Advances of Efficient Small Molecule Donors Based on Benzodithiophene and Its Derivatives
    YANG Ke, XIAO Zeyun, LU Shirong, SUN Kuan
    Chem. J. Chinese Universities    2023, 44 (9): 20230123-.   DOI: 10.7503/cjcu20230123
    Abstract683)   HTML74)    PDF(pc) (7096KB)(5867)       Save

    The rapid development of all-small-molecule solar cell has recently gained recognition within the photovoltaic research community. Well-defined structure and less batch-to-batch variation empowered it great application prospects. In this perspective, we review the development of small molecule donors based on benzodithiophene(BDT) and its derivatives, with a focus on the relationship between molecule structure, stacking characteristics and device performance. By analyzing successful cases in the BDT series of small molecules, we aim to clarify the link between molecule structure, solid-state aggregation and device performance. We hope this discussion can be the minnow to catch the whale of highly efficient molecules in the future.

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    Design, Synthesis and Fungicidal Activity of Pyrazinamide Analogs
    WANG Gang, LIANG Shuang, SHAN Zhonggang, YING Junwu, LYU Liang, LI Bin, YANG Huibin
    Chem. J. Chinese Universities    2024, 45 (10): 20240369-.   DOI: 10.7503/cjcu20240369
    Abstract629)   HTML93)    PDF(pc) (4355KB)(5841)       Save

    Pyraziflumid was a novel pyrazinamide analog fungicide developed by Nihon Nohyaku Co. In this work, 16 pyrazinamide analogs were synthesized using substituted pyrazine acid and 2-methyl-3-nitrophenol as initial materials through 4 steps. The structures of the target compounds were confirmed by nuclear magnetic resonance (1H NMR, 13C NMR) and high resolution mass spectrometer(HRMS). The results of fungicidal activity at greenhouse showed that pyrazinamide analogs had excellent fungicidal activities against corn rust at 6.25 mg/L. Among them, the fungicidal activities of compounds 457815 and 16 against corn rust at 6.25 mg/L were 100%. Molecular docking simulations revealed that compound 16 interacted with TRP-173 of succinate dehydrogenase(SDH) through hydrogen bonding, which could explain the probable mechanism of action between compound 16 and the target protein. These results indicated that compound 16 might be a promising fungicide candidate and provide valuable reference for further investigation.

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    Advances in Alloy-based High-capacity Li-containing Anodes for Lithium-ion Batteries
    MAO Eryang, WANG Li, SUN Yongming
    Chem. J. Chinese Universities    2021, 42 (5): 1552-1568.   DOI: 10.7503/cjcu20200750
    Abstract1979)   HTML158)    PDF(pc) (7469KB)(5706)       Save

    The emergent Li-containing alloys(LixMy, M refers to metal or nonmetal element that can react with Li to form alloys) is a class of promising electrode materials for next-generation high energy lithium-ion batteries. They deliver high theoretical specific capacities that are several times that of current graphite and can act as active lithium suppliers that are different from traditional lithium-free alloy anodes(Si, Sn, P, etc.). The LixMy anodes can pare with high-capacity Li-free cathodes(such as Sulfur, O2, FeF3, V2O5, etc.) to develop a new full battery system. In this paper, researches on Li-containing alloy-based high-capacity anodes LixMy(e.g., Li4.4Si, Li4.4Sn, Li3P, Li2.25Al, etc.) were reviewed. Scientific challenges and technical difficulties of LixMy anodes were systematically analyzed and discussed. Various methods for materials synthesis and electrodes fabrication were summarized. Furthermore, various full-cell configurations based on LixMy anodes were introduced, including Li-ion batteries(LIBs), Li-ion-sulfur batteries(LISBs), and Li-ion-oxygen batte-ries(LIOBs). Moreover, research strategies and achievements on addressing the challenges of LixMy anodes and improving their performance were discussed, including composition adjustment, surface coating, material composite, electrode treatment, and electrolyte engineering, etc. Also, perspectives and new insights for the future development of LixMy anodes are proposed.

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    Rapid Grafting of Phenylboronic Acid with Hydroxypropyl Chitosan Mediated by HATU
    LI Aoqi, HU Chuanzhi, SHI Han, DENG Mingyu, XIAO Bo, JIANG Bo
    Chem. J. Chinese Universities    2023, 44 (6): 20220698-.   DOI: 10.7503/cjcu20220698
    Abstract1501)   HTML110)    PDF(pc) (1100KB)(5657)       Save

    Phenylboronic acid(PBA) can form reversible covalent bonds with cis-1,2-diol or 1,3-diol in an aqueous solution, which makes it useful as the glucose-responsive units or dynamic cross-linking groups in nano/hydrogels. In this paper, PBA was efficiently grafted on hydroxypropyl chitosan(HPCS) by employing 2-(7-azabenzotriazol-1-yl)- NNN',N'-tetramethyluronium hexafluorophosphate(HATU) as a coupling reagent in dimethyl sulfoxide(DMSO). The resulting carboxyphenylboronic acid-grafted hydroxypropyl chitosan(CPBA-HPCS) was soluble when pH>8.5, and the structure was characterized and confirmed by Fourier-transform infrared spectroscopy(FTIR) and nuclear magnetic resonance(NMR). In addition, the kinetics of the reaction were studied and a series of CPBA-HPCS with different substitution degrees(up to 0.78) was prepared. This novel chitosan derivative has good application prospects in the preparation of smart hydrogels and drug carriers.

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    CuBi2O4/Bi2WO6 Z-type Heterostructures for Effective Removal Ciprofloxacin in Photo-electro-Fenton-like System
    WANG Qiuxia, HAN Yugui, ZHAO Peng, WANG Shuang, LIU Yaru, LI Yi
    Chem. J. Chinese Universities    2024, 45 (1): 20230370-.   DOI: 10.7503/cjcu20230370
    Abstract892)   HTML82)    PDF(pc) (7287KB)(5303)       Save

    In response to the serious problem of antibiotic pollution in the current water environment, herein, a CuBi2O4/Bi2WO6(CBWO) Z-type heterojunction photoelectric catalyst was synthesized by a simple solvothermal method. The morphology and structure were obtained through SEM, which showed that the structure of the CBWO-60 was cuboid rod-like morphology and nanosheet. The EDS elemental mapping images displayed that Cu, W, Bi and O elements were evenly dispersed in CBWO-60. The crystalline phases and molecular structures of the catalyst were determined by XRD and FTIR. These results firmly confirmed that the successful synthesis of the composite. The large specific surface area of CBWO-60 was investigated via BET. XPS analysis proved that the Cu+ and Cu2+ coexisted, which promoted the cycling of Fenton reaction. Moreover, the displacement of binding energy well verified the strong electronic interaction rather than a physical contact between CuBi2O4 and Bi2WO6 in the heterojunction. The band structure of the heterojunction was proved by UV-Vis DRS and VB-XPS analysis. The interface charge transfer situation of the heterojunction was investigated by PL, EIS, and transient photocurrent response spectra. In a series of catalysts, CBWO-60 has the highest degradation efficiency for Ciprofloxacin(CIP) in the photo-electro- Fenton-like(PEF-like) system, with a degradation efficiency of 98.0% at 90 min. At the same time, when the initial pH of the solution was in the range of 2—6, the system could always maintain effective CIP removal efficiency. The pH range of this system was broadened to some extent compared to the conventional Fenton method. In the PEF-like system, CBWO-60 showed high catalytic activity to quinolone, sulfonamides and tetracycline antibiotics, which proved the universality of CBWO-60. Finally, the degradation efficiency of CIP still maintained 87.8% after five cycles of experiments, and the crystal structure of CBWO-60 remained unchanged after the reaction. Based on the results of HPLC-MS, five possible pathways for CIP degradation were proposed. This study provided a new idea for the purification and treatment of antibiotic pollution in the water environment.

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    Preparation, Characterization and Drug Release of Biodegradable Solid Lipid Nanoparticles
    GUAN Qing-Xiang, ZHU Kun, LIN Tian-Mu, GUAN Qing-Tao, GUO Jie*, YIN Jian-Yuan*
    Chem. J. Chinese Universities    2010, 31 (11): 2298-2302.  
    Abstract3469)      PDF(pc) (581KB)(5276)       Save
    Biodegradable solid lipid nanoparticles loaded with pueraria flavones(PF-SLN) were prepared by emulsification evaporation-solidification at low temperature with a biodegradable material, stearic acid as the carrier. The morphology and particle size of PF-SLN were measured by TEM and laser light scattering technique, respectively. The physical status of the drug in PF-SLN was analyzed by X-ray powder diffractometry. Its entrapment efficacy in SLN and release were also investigated. PF-SLN is near spherical in shape and the average diameter is (263.82±3.6) nm. Its entrapment effciency (EE) is (67.53±0.12)%. X-ray powder diffraction analysis results show that the pueraria flavones are dispersed with the state of molecular or tiny particles in the matrix of SLN. The results show that the release of PF-SLN occurs rapidly in the early stage and then slowly which accumulate up to 50% in 12 h . The drug release slowly from SLN following matrix erosion. The release profile fits well to the Higuchi equation.
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    Cited: Baidu(4)
    Recent Advance of Hydrothermal Growth of ZnO and TiO2 Nano-tree Arrays
    ZHAO Feng-Hua YANG Xian-Feng GAO Qiong, WU Ming-Mei*
    Chem. J. Chinese Universities    2011, 32 (3): 451-461.  
    Abstract4034)      PDF(pc) (11044KB)(5271)       Save
    Branched tree-like nanoarrays are emerging as an exciting addition to the family of oriented semiconducting nanomaterials. Besides high temperature solid state and vapor-liquid-solid (VLS), a site-specific sequential nucleation and growth route to the systematic building of hierarchical, complex, and oriented ZnO micro/nanostructures in solution synthesis has been developed. Herein, we present a one-step, low cost, and environment-benign route to growing large-scale arrays of zinc oxide and titanium dioxide by solution chemistry. The growth mechanism and their possible applications have been suggested.
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    Cited: Baidu(5)
    Cover and Content of Chemical Journal of Chinese Universities Vol.34 No.1(2013)
    Chem. J. Chinese Universities    2013, 34 (1): 0-0.  
    Abstract1686)      PDF(pc) (16401KB)(5143)       Save
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    Fundamental Flaw of Marcus Theory
    ZHU Xiao-Qing, YANG Jin-Dong
    Chem. J. Chinese Universities    2013, 34 (10): 2247-2253.   DOI: 10.7503/cjcu20130183
    Abstract7731)      PDF(pc) (1419KB)(5048)       Save

    Marcus theory is a theory originally developed by Rudolph A. Marcus in 1956 based on Libby's idea about electron transfer mechanism according to the two-sphere model with the help of the continuous medium theory and the electrostatic mechanics to describe the kinetics of the outer-sphere electron transfer reactions in solution, which states that the activation free energies of the outer-sphere electron transfer reactions have the quadratic relationship with the corresponding reaction free energy changes. Having been developed by Marcus and many other chemists for more than 50 years, Marcus theory has received extensive application in various fields. Meanwhile, the research object of Marcus theory has been extended from the outer-sphere electron transfer reactions to the inner-sphere electron transfer reactions, even more to the nucleus transfer reactions. Because the reaction coordinates of the transition state of the electron transfer reactions in Marcus inverted region go beyond the region between the initial state and the final state of the reactions in the same reaction coordinate system, which evidently does not obey the natural change logic, we have never accepted Marcus theory as a scientific theory, even though some experimental observations were reported by Miller and Closs as well as many other chemists to support Marcus inverted region. In order to dig out the origin of Marcus theory error, in this study we examined the following questions about the classical Marcus theory:(1) What are the prerequisites(or assumptions) of Marcus theory? (2) How do Marcus free energy parabolas for the reactant system and for the product system form? (3) What factors determine the feature of Marcus free energy parabolas? (4) How does the classical Marcus equation form? (5) What is the criterion of Marcus inverted region? After the examinations, the following conclusions can be made:(1) Marcus theory directly conflicts with the law of conservation of energy and has the error in principle; (2) Marcus inverted region is impossible; (3) the experimental observations for Marcus inverted region reported in the literatures are all spurious.

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    Cited: Baidu(1)
    Perovskite Solar Cells: Work Mechanism and Major Factors Affecting Their Performances
    QIAN Liu, DING Liming
    Chem. J. Chinese Universities    2015, 36 (4): 595-607.   DOI: 10.7503/cjcu20140927
    Abstract6615)   HTML124)    PDF(pc) (5173KB)(4771)       Save

    Hybrid organic-inorganic perovskites were first introduced to photovoltaic community in 2009. In subsequent years, the power conversion efficiency has increased from 3.8% to ~20%, leaving dye-sensitized solar cells and bulk-heterojunction solar cells far behind. “Perovskite” is a crystal possessing the same crystal structure as calcium titanate, namely, ABX3. Perovskites have unique properties, like broad absorption spectra, high absorption coefficient, ambipolar charge transport, long exciton lifetime and very low binding energy of exciton. Currently, the architecture of perovskite solar cells has been simplified from meso-structured solar cells to planar-heterojunction solar cells, getting closer to the low-cost, high-efficiency target for practical application. Many innovative researches are pushing the application of this new photovoltaic material to the climax. This review summarizes the working mechanism of perovskite solar cells and expounds several key factors affecting device performance, i.e. components, crystallization and morphology, transport layers, electrode materials and planted bulk-heterojunction. However, we should note that perovskites have some drawbacks impeding its commercialization. Perovskites are sensitive to oxygen and water vapor, making the solar cells unstable in the ambient; it is challenging to prepare large films because the morphology of perovskite film is difficult to control; the use of the toxic metal, lead, will also undermine the credit earned by their outstanding photovoltaic performance. It is very important for us to understand those mechanism and factors affecting device performance, and to find approaches to deal with instability, toxicity, and bad morphology.

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    Synthesis of Nitrogen-doped Graphene and Its Electrocatalytic Performance Toward Oxygen Reduction Reaction
    LI Jing, WANG Xian-Bao, YANG Jia, YANG Xu-Yu, WAN Li
    Chem. J. Chinese Universities    2013, 34 (4): 800-805.   DOI: 10.7503/cjcu20120658
    Abstract5980)      PDF(pc) (2932KB)(4763)       Save

    A series nGs with different electrocatalytic abilities toward oxygen reduction reaction(ORR) was prepared via a two-steps pyrolysis method by controlling the reaction temperature on the physical mixture of graphene oxideand urea. Transmission electron microscopy and scanning electron microscopy display nG with highly wrinkled and overlapping structures. X-ray photoelectron spectroscopy shows that nitrogen is successfu-lly doped in graphene with the formation of pyridinic N, pyrrolic N and graphitic N, and the maximum nitrogen content is 6.6%(molar fraction). Cyclic voltammogram and rotating disk electrode measurement show that nGs exhibit high electrocatalytic activity with an onset potential of 0.1 V in an acid electrolyte. Moreover, the nGs catalyzed oxygen reduction revealed a favorable formation of water via a four-electron pathway and excellent stability over Pt/C catalyst. Furthermore, the nG obtained at 200 ℃ in the first pyrolysis step displays the best catalytic perfor-mance.

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    Cited: Baidu(18)