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| 1 | Photocatalytic enhancement of Mg-doped ZnO nanocrystals hybridized with reduced graphene oxide sheets显示文摘Hybridization of Mg-doped ZnO and reduced graphene oxide(MZO–RGO) were synthesized through one pot reaction process. Crystallization of MZO–RGO upon thermal decomposition of the stearate precursors was investigated by X-ray diffraction technique. XRD studies point toward the particles size with 10–15 nm,which was confirmed by transmittance electronic microscopy,and also indicates that graphene oxide has been directly reduced into its reduced state graphene during the synthesis. Graphene hybridized MZO photocatalyst showed enhanced catalytic activity for the degradation of methylene blue(MB). The degree of photocatalytic activity enhancement strongly depended both on the coverage of graphene on the surface of MZO nanoparticles and the Mg doping concentration. The sample of 2 wt% graphene hybridized 5 at% Mg-doped ZnO showed the highest photocatalytic activity,which remained good photocatalytic activity after nine cycling runs. | Linqin Wang Yan Wun Fangyuan Chen Xiang Yang | 2014 | Progress in Natural Science:Materials International2014，24，1： | 3 |
| 2 | Nonlinear dynamics behaviors of a rotor roller bearing system with radial clearances and waviness considered 显示文摘 | WANG Linqin CUI Li ZHENG Dezhi | 2008 | Journal of Aeronautics2008，21，1： | 1 |
| 3 | Orbital-regulated interfacial electronic coupling endows Ni3N with superior catalytic surface for hydrogen evolution reaction显示文摘The interstitial structure and weak Ni-N interaction of Ni3N lead to high unoccupied d orbital energy and unsuitable orbital orientation,which consequently results in weak orbital coupling with H2O and slow water dissociation kinetics for alkaline hydrogen evolution catalysis.Herein,we successfully lower the unoccupied d orbital energy of Ni3N to strengthen the interfacial electronic coupling by employing the strong electron pulling capability of oxygen dopants.The prepared O-Ni3N catalyst delivers an overpotential of 55 mV at 10 mA cm−2,very close to the commercial Pt/C.Refined structural characterization indicates the oxygen incorporation can decrease the electron densities around the Ni sites.Moreover,density functional theory calculation further proves the oxygen incorporation can create more unoccupied orbitals with lower energy and superior orientation for water adsorption and dissociation.The concept of orbital-regulated interfacial electronic coupling could offer a unique approach for the rational design of hydrogen evolution catalysts and beyond. | Yanyan Fang Da Sun Shuwen Niu Jinyan Cai Yipeng Zang Yishang Wu Linqin Zhu Yufang Xie Yun Liu Zixuan Zhu Amirabbas Mosallanezhad Di Niu Zheng Lu Junjie Shi Xiaojing Liu Dewei Rao Gongming Wang Yitai Qian | 2020 | Science China Chemistry2020，63，11： | 1 |
| 4 | Switching O-O bond formation mechanism between WNA and I2M pathways by modifying the Ru-bda backbone ligands of water-oxidation catalysts显示文摘Understanding the seven coordination and O-O coupling pathway of the distinguished Ru-bda catalysts is essential for the development of next generation efficient water-oxidation catalysts based on earthabundant metals.This work reports the synthesis,characterization and catalytic properties of a monomeric ruthenium catalyst Ru-bnda(H2 bnda=2,2’-bi(nicotinic acid)-6,6’-dicarboxylic acid)featuring steric hindrance and enhanced hydrophilicity on the backbone.Combining experimental evidence with systematic density functional theory calculations on the Ru-bnda and related catalysts Ru-bda(H_(2)bda=2,2’-bipyridine-6,6’-dicarboxylic acid),Ru-pda(H_(2)pda=1,10-phenanthroline-2,9-dicarboxylic acid),and Ru-biqa(H_(2)biqa=(1,1’-biisoquinoline)-3,3’-dicarboxylic acid),we emphasized that seven coordination clearly determines presence of Ru^(Ⅴ)=O with high spin density on the ORu^(Ⅴ)=O atom,i.e.oxo with radical properties,which is one of the necessary conditions for reacting through the O-O coupling pathway.However,an additional factor to make the condition sufficient is the favorable intermolecular faceto-face interaction for the generation of the pre-reactive[Ru^(Ⅴ)=O…O=Ru^(Ⅴ)],which may be significantly influenced by the secondary coordination environments.This work provides a new understanding of the structure-activity relationship of water-oxidation catalysts and their potential to adopt I2M pathway for O-O bond formation. | Biaobiao Zhang Shaoqi Zhan Tianqi Liu Linqin Wang A.Ken Inge Lele Duan Brian J.J.Timmer Oleksandr Kravchenko Fei Li Marten S.G.Ahlquist Licheng Sun | 2021 | Journal of Energy Chemistry2021，30，3： | 1 |
| 5 | Determi- nation of ammonia in waters using flow injection analy- sis with automatic pervoperation enrichment显示文摘 | Hong Lingcheng Sun Xiyan Wang Linqin | 2009 | Anal lett2009，42，15： | 1 |
| 6 | Isolation and Identification of Pseudo Seven-Coordinate Ru(Ⅲ)Intermediate Completing the Catalytic Cycle of Ru-bda Type of Water Oxidation Catalysts显示文摘Isolation of RuⅢ-bda(17-electron specie)complex with an aqua ligand(2-electron donor)is challenging due to violation of the 18-electron rule.Although considerable efforts have been dedicated to mechanistic studies of water oxidation by the Ru-bda family,the structure and initial formation of the Ru^(Ⅲ)-bda aqua complex are still controversial.Herein,we challenge this often overlooked step by designing a pocketshape Ru-based complex 1.The computational studies showed that 1 possesses the crucial hydrophobicity at the Ru^(V)(O)state as well as similar probability of access of terminal O to solvent water molecules when compared with classic Ru-bda catalysts.Through characterization of single-crystal structures at the Ru^(Ⅱ) and Ru^(Ⅲ) states,a pseudo seven-coordinate“ready-togo”aqua ligand with Ru^(Ⅲ)…O distance of 3.62A was observed.This aqua ligand was also found to be part of a formed hydrogen-bonding network,providing a good indication of how the Ru^(Ⅲ)-OH_(2)complex is formed. | Tianqi Liu Ge Li Nannan Shen Linqin Wang Brian J.J.Timmer Shengyang Zhou Biaobiao Zhang Alexander Kravchenko Bo Xu Marten S.G.Ahlquist Licheng Sun | 2022 | CCS Chemistry2022，4，7： | 1 |
| 7 | In-depth understanding the effect of electron-withdrawing/-donating groups on the interfacial carrier dynamics in naphthalimide-treated perovskite solar cells显示文摘Surface defect passivation of perovskite films through chemical interaction between specific functional groups and defects has been proven to be an effective technique for enhancing the performance and stability of perovskite solar cells(PSCs).However,an in-depth understanding of how these passivation materials affect the intrinsic nature of charge-carrier transfer kinetics in PSCs remains shielded so far.Herein,we have designed two naphthalimide-based perovskite surface passivators having electronwithdrawing(-CF_(3),NSF)or electron-donating(-CH_(3),NSC)substituents for use in PSCs.Transient absorption spectroscopy(TA)measurements confirmed how the electron-withdrawing and electron-donating groups can efficiently turn the hot carriers(HCs)cooling and injection,and interface recombination in the device.We found that NSC-passivated perovskite samples exhibit faster hot-carriers(HCs)injection from the perovskite layer into carrier transport layers before cooling to the crystal lattice compared with the NSF-based and control ones with the order:NSC>NSF>control.Fast HCs injection is advantageous to minimize the charge-carriers recombination and improve PSCs performance.The carrier lifetime in NSCtreated device measured by nanosecond TA exhibits nearly~2 times longer than that of NSF-based device,which demonstrates the decreased charge-carrier recombination in NSC-treated device.As expected,the power conversion efficiency(PCE)of the NSC-treated PSCs is improved to 23.04%compared with that of the device treated with NSF(21.81%).Our findings provide invaluable guide for developing highly efficient passivators to further boost PSCs photovoltaic performance. | Tai Wu Rongjun Zhao Donglin Jia Linqin Wang Xiaoliang Zhang Licheng Sun Yong Hua | 2023 | Journal of Energy Chemistry2023，，2： | 0 |
| 8 | A crosslinked polymer as dopant-free hole-transport material for efficient n-i-p type perovskite solar cells显示文摘A new crosslinked polymer,called P65,with appropriate photo-electrochemical,opto-electronic,and thermal properties,has been designed and synthesized as an efficient,dopant-free,hole-transport material(HTM)for n-i-p type planar perovskite solar cells(PSCs).P65 is obtained from a low-cost and easily synthesized spiro[fluorene-9,90-xanthene]-30,60-diol(SFX-OH)-based monomer X65 through a freeradical polymerization reaction.The combination of a three-dimensional(3 D)SFX core unit,holetransport methoxydiphenylamine group,and crosslinked polyvinyl network provides P65 with good solubility and excellent film-forming properties.By employing P65 as a dopant-free hole-transport layer in conventional n-i-p type PSCs,a power conversion efficiency(PCE)of up to 17.7%is achieved.To the best of our knowledge,this is the first time a 3 D,crosslinked,polymeric dopant-free HTM has been reported for use in conventional n-i-p type PSCs.This study provides a new strategy for the future development of a 3 D crosslinked polymeric dopant-free HTM with a simple synthetic route and low-cost for commercial,large-scale applications in future PSCs. | Linqin Wang Fuguo Zhang Tianqi Liu Wei Zhang Yuanyuan Li Bin Cai Lanlan He Yu Guo Xichuan Yang Bo Xu James M.Gardner Lars Kloo Licheng Sun | 2021 | Journal of Energy Chemistry2021，30，4： | 0 |
| 9 | Recent progress in room-temperature sodium-ion batteries显示文摘Room-temperature sodium-ion batteries have attracted increasing interest in recent years because of abundant sodium reserves and the low costs.Grid-scale energy storage applications are particularly relevant to this battery technology.Here,we present our recent progress in researching room-temperature sodium-ion batteries,and focus on new electrode materials,including cathodes and anodes,for both non-aqueous and aqueous systems. | WU XiaoYan YU JueZhi WANG YueSheng MU LinQin HU YongSheng CHEN LiQuan | 2014 | Science Foundation in China2014，22，1： | 0 |
| 10 | Highly stable perovskite solar cells with a novel Ni-based metal organic complex as dopant-free hole-transporting material显示文摘Hole-transporting material(HTM)plays a paramount role in enhancing the photovltaic performance of perovskite solar cells(PSCs).Currently,the vast majority of these HTMs employed in PSCs are organic small molecules and polymers,yet the use of organic metal complexes in PSCs applications remains less explored.To date,most of reported HTMs require additional chemical additives(e.g.Li-TFSI,t-TBP)towards high performance,however,the introduction of additives decrease the PSCs device stability.Herein,an organic metal complex(Ni-TPA)is first developed as a dopant-free HTM applied in PSCs for its facile synthesis and efficient hole extract/transfer ability.Consequently,the dopant-free Ni-TPAbased device achieves a champion efficiency of 17.89%,which is superior to that of pristine Spiro-OMeTAD(14.25%).Furthermore,we introduce a double HTM layer with a graded energy bandgap containing a Ni-TPA layer and a CuSCN layer into PSCs,the non-encapsulated PSCs based on the Ni-TPA/CuSCN layers affords impressive efficiency up to 20.39%and maintains 96%of the initial PCE after 1000 h at a relative humidity around 40%.The results have demonstrated that metal organic complexes represent a great promise for designing new dopant-free HTMs towards highly stable PSCs. | Tai Wu Linqin Wang Rongjun Zhao Rongshan Zhuang Kanghong Zhao Gaoyuan Liu Jing Huang Licheng Sun Yong Hua | 2022 | Journal of Energy Chemistry2022，31，2： | 0 |
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