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| 1 | Query processing in multi - user scenario for wireless sensor networks 显示文摘 | Liu Xingcheng Ma Zaili | 2011 | IEEE Sensors Journal2011，11，3： | 1 |
| 2 | Query processing in multi-user scenario for Wireless Sensor Networks显示文摘 | Liu Xingcheng Ma Zaili Liu Shaochong | 2011 | IEEE Sensors Journal2011，11，10： | 1 |
| 3 | A simple solvothermal reduction route to copper and cuprous oxide显示文摘 | Wei Mingzhen Lun Ning Ma Xingcheng | 2007 | Mater Lett2007，61，1112： | 1 |
| 4 | Stoichiometric flexibility regulates the co-metabolism effect during organic carbon mineralization in eutrophic lacustrine sediments显示文摘Several studies have suggested the pivotal roles of eutrophic lakes in carbon(C)cycling at regional and global scales.However,how the co-metabolism effect on lake sediment organic carbon(OC)mineralization changes in response to integrated inputs of labile OC and nutrients is poorly understood.This knowledge gap hinders our ability to predict the carbon sequestration potential in eutrophic lakes.Therefore,a 45-day microcosm experiment was conducted to examine the dominant mechanisms that underpin the co-metabolism response to the inputs of labile C and nutrients in lacustrine sediments.Results indicate that the labile C addition caused a rapid increase in the positive co-metabolism effect during the initial stage of incubation,and the co-metabolism effect was positively correlated with the C input level.The positive co-metabolism effect was consistently higher under high C input,which was 152%higher than that under low C input.The higherβ-glucosidase activity after nutrient addition,which,in turn,promoted the OC mineralization in sediments.In addition different impacts of nutrients on the co-metabolism effect under different C inputs were observed.Compared with the low nutrient treatments,the largest co-metabolism effect under high C with high nutrient treatment was observed by the end of the incubation.In the high C treatment,the intensity of the co-metabolism effect(CE)under high nitrogen treatment was 1.88 times higher than that under low nitrogen condition.However,in the low C treatment,the amount of nitrogen had limited impact on co-metabolism effect.Our study thus proved that the microorganisms obviously regulate sediment OC turnover via stoichiometric flexibility to maintain a balance between resources and microbial requirements,which is meaningful for evaluating the OC budget and lake eutrophication management in lacustrine sediments. | Jie MA Fei HE Xingcheng YAN Ruijie SHI Ming JI Bin XU Xiaodong WU Zhichun LI Xiaoguang XU Guoxiang WANG | 2022 | Journal of Oceanology and Limnology2022，40，5： | 0 |
| 5 | Applying machine-learning screening of single transition metal atoms anchored on N-dopedγ-graphyne for carbon monoxide electroreduction toward C_(1)products显示文摘Carbon monoxide electroreduction(COER)has been a key part of tandem electrolysis of carbon dioxide(CO_(2)),in which searching for high catalytic performance COER electrocatalysts remains a great challenge.Herein,by means of density functional theory(DFT)computations,we explored the potential of a series of transition metal atoms anchored on N-dopedγ-graphyne(TM@N-GY,TM from Ti to Au)as the COER electrocatalysts.We found that the final product selectivity of these single-atom catalysts depended on the position of the metal atom in the periodic table,with metals in the front and middle of each periodic period exhibiting high selectivity for CH_(4),while metals in the back producing CH_(3)OH.Machine learning(ML)found that metal atomic number was intrinsic to the difference in COER performance of these single-atom catalysts(SACs).The free energy changes showed that Mn@N-GY and Ni@N-GY exhibited outstanding COER catalytic performance for producing CH_(4)and CH_(3)OH,respectively.Our results provide theoretical and experimental guidance for designing efficient COER catalysts to generate C_(1)products. | Dongxu Jiao Dantong Zhang Dewen Wang Jinchang Fan Xingcheng Ma Jingxiang Zhao Weitao Zheng Xiaoqiang Cui | 2023 | Nano Research2023，16，8： | 0 |
| 6 | Phenylformamidinium-enabled quasi-2D Ruddlesden-Popper perovskite solar cells with improved stability显示文摘Two-dimensional(2D)/quasi-2D perovskite solar cells(PSCs)incorporating organic spacer cations exhibit appealing ambient stability in comparison with their 3D analogs.Most reported organic spacer cations are based on ammonium,whereas formamidinium(FA^(+))has been seldom applied despite that FA has been extensively used in high-efficiency 3D PSCs.Herein,a novel FA-based organic spacer cation,4-chloro-phenylformamidinium(CPFA^(+)),is applied in quasi-2D Ruddlesden-Popper(RP)PSCs for the first time,and methylammonium chloride(MACl)is employed to promote crystal growth and orientation of perovskite film,resulting in high power conversion efficiency(PCE)with improved stability.Upon incorporating CPFA+organic spacer cation and MACl additive,high-quality quasi-2D CPFA_(2)MA_(n-1)Pb_(n)(I_(0.857)Cl_(0.143))_(3n+1)(n=9)perovskite film forms,exhibiting improved crystal orientation,reduced trap state density,prolonged carrier lifetime and optimized energy level alignment.Consequently,the CPFA_(2)MA_(n-1)Pb_(n)(I_(0.857)Cl_(0.143))_(3n+1)(n=9)quasi-2D RP PSC devices deliver a highest PCE of 14.78%.Moreover,the un-encapsulated CPFA-based quasi-2D RP PSC devices maintain~80%of its original PCE after exceeding 2000 h storage under ambient condition,whereas the 3D MAPb I3counterparts retain only~45%of its original PCE.Thus,the ambient stability of quasi-2D RP PSC devices is improved obviously relative to its 3D MAPb I3counterpart. | Xingcheng Li Wanpei Hu Yanbo Shang Xin Yu Xue Wang Weiran Zhou Mingtai Wang Qun Luo Chang-Qi Ma Yalin Lu Shangfeng Yang | 2022 | Journal of Energy Chemistry2022，31，3： | 0 |
| 7 | Atomic Dispersed Hetero‑Pairs for Enhanced Electrocatalytic CO_(2)Reduction显示文摘Electrochemical carbon dioxide reduction reaction(CO_(2)RR)involves a variety of intermediates with highly correlated reaction and ad-desorption energies,hindering optimization of the catalytic activity.For example,increasing the binding of the*COOH to the active site will generally increase the*CO desorption energy.Breaking this relationship may be expected to dramatically improve the intrinsic activity of CO_(2)RR,but remains an unsolved challenge.Herein,we addressed this conundrum by constructing a unique atomic dispersed hetero-pair consisting of Mo-Fe di-atoms anchored on N-doped carbon carrier.This system shows an unprecedented CO_(2)RR intrinsic activity with TOF of 3336 h−1,high selectivity toward CO production,Faradaic efficiency of 95.96%at−0.60 V and excellent stability.Theoretical calculations show that the Mo-Fe diatomic sites increased the*COOH intermediate adsorption energy by bridging adsorption of*COOH intermediates.At the same time,d-d orbital coupling in the Mo-Fe di-atom results in electron delocalization and facilitates desorption of*CO intermediates.Thus,the undesirable correlation between these steps is broken.This work provides a promising approach,specifically the use of di-atoms,for breaking unfavorable relationships based on understanding of the catalytic mechanisms at the atomic scale. | Zhaoyong Jin Meiqi Yang Yilong Dong Xingcheng Ma Ying Wang Jiandong Wu Jinchang Fan Dewen Wang Rongshen Xi Xiao Zhao Tianyi Xu Jingxiang Zhao Lei Zhang David J.Singh Weitao Zheng Xiaoqiang Cui | 2024 | Nano-Micro Letters2024，16，1： | 0 |
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