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Probing surface interactions of underwater oleophobic polyelectrolyte multilayers 被引量:1
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作者 Kai Li Wei Wang +7 位作者 zhi-peng yu Hang Jin yun-Tong Ge Wei-Wei Gao Fan Xiao Hui-Rong Huang Ze-Heng Peng Jing Gong 《Petroleum Science》 SCIE CAS CSCD 2021年第1期307-321,共15页
In the present work,the interaction mechanism of specific polyelectrolyte multilayers(PEMs),fabricated by layer-by-layer deposition of polydiallyldimethylammonium chloride(PDDA)and poly(sodium 4-styrenesulfonate)(PSS)... In the present work,the interaction mechanism of specific polyelectrolyte multilayers(PEMs),fabricated by layer-by-layer deposition of polydiallyldimethylammonium chloride(PDDA)and poly(sodium 4-styrenesulfonate)(PSS),is studied using atomic force microscopy.The underwater oil-repellency of PS S-capped PEMs was further explored by measuring the interaction forces between tetradecane droplets and PEMs-coated silica substrates under various salinities.The force curves were analyzed following the Stokes-Reynolds-Young-Laplace theoretical model.Desirable consistency was achieved between the experimental and theoretical calculations at low NaCl concentrations(0.1 mM and 1 mM);however,underestimation of the attractive force was found as the NaCl concentration increases to moderate(10 mM)and high(100 mM)levels.Discrepancy analyses and incorporated features toward a reduced surface charge density were considered based on the previous findings of the orientation of anionic benzenesulfonate moieties(Liu et al.in Angew Chem Int Ed 54(16):4851-4856,2015.https://doi.org/10.1002/anie.201411992).Short-range steric hindrance interactions were further introduced to simulate"brush"effect stemming from nanoscale surface roughness.It is demonstrated in our work that the PSS-capped PEMs remains a stable underwater lipophobicity against high salinity,which renders it potential application in surface wetting modification and anti-fouling. 展开更多
关键词 Lipophobicity SALINITY AFM Polyelectrolyte multilayers Surface roughness
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Mechanical properties and microstructure evolution of solidified copper tailings with hydantoin epoxy resin 被引量:1
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作者 Yong HE Wen-qiang JIANG +5 位作者 Ke-ping CHEN Lian-rong WU Ke-neng ZHANG zhi-peng yu Xue-ping GAN De-shan FENG 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2022年第9期3065-3076,共12页
Based on the strength and microstructure tests,the effects of the hydantoin epoxy resin content and curing time on the mechanical properties and microstructure of copper tailings specimens were studied.The results sho... Based on the strength and microstructure tests,the effects of the hydantoin epoxy resin content and curing time on the mechanical properties and microstructure of copper tailings specimens were studied.The results showed that the strength of the solidified specimens was increased to 20.84 MPa with 30 wt.%addition of hydantoin epoxy resin.When the specimens with 10%hydantoin epoxy resin were cured for 7 and 14 d,the strengths were 6.33 and 6.67 MPa respectively,which met the requirements as foundation filler and building materials.The microscopic tests showed that the agglomeration was enhanced and the porosities of the solidified specimens were reduced with increase in the hydantoin epoxy resin content,which could greatly enhance the strength of solidified specimens. 展开更多
关键词 copper tailings hydantoin epoxy resin mechanical properties MICROSTRUCTURE
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用于硝基苯选择性加氢催化的钯镍合金/氮化镍界面构筑
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作者 吴静波 高亚男 +3 位作者 段万春 杜先婷 余志鹏 徐坤 《Science China Materials》 SCIE EI CAS CSCD 2023年第9期3565-3572,共8页
金属负载型催化剂的界面结构设计一直是实现高效、高选择性催化反应的核心研究.本文表明,异质结结构PdNi&Ni_(3)N的界面电荷重新分布可以催化硝基苯选择性加氢成为偶氮类化合物.相比之下,独立的PdNi合金催化硝基苯转化为苯胺,而Ni_(... 金属负载型催化剂的界面结构设计一直是实现高效、高选择性催化反应的核心研究.本文表明,异质结结构PdNi&Ni_(3)N的界面电荷重新分布可以催化硝基苯选择性加氢成为偶氮类化合物.相比之下,独立的PdNi合金催化硝基苯转化为苯胺,而Ni_(3)N载体在相同条件下对硝基苯加氢的催化几乎没有效果. X射线光电子能谱和理论计算表明,PdNi&Ni_(3)N界面电荷重新分布导致有机反应中间体的吸附能发生变化,从而改变加氢反应途径,实现偶氮化合物的高选择性生成.本研究进一步表明了界面结构设计在有机催化加氢反应中的重要性,而且可能会引起研究者对于异质结构金属(合金)/过渡金属氮化物更多的科学兴趣,以应用于催化领域的不断发展. 展开更多
关键词 负载型催化剂 偶氮化合物 X射线光电子能谱 加氢反应 选择性加氢 过渡金属氮化物 吸附能 界面结构
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High-efficiency organic solar cells with low voltage-loss of 0.46 V 被引量:1
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作者 zhi-peng yu Xue Li +8 位作者 Chengliang He Di Wang Ran Qin Guanqing Zhou Zhi-Xi Liu Thomas Rieks Andersen Haiming Zhu Hongzheng Chen Chang-Zhi Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2020年第7期1991-1996,共6页
The recent evolution of active components yielded brilliant progresses for organic solar cells(OSCs),yet the mechanism is needed to be clearly understood.In this wo rk,two electron acceptors,a linear SN6-2Br and a V-s... The recent evolution of active components yielded brilliant progresses for organic solar cells(OSCs),yet the mechanism is needed to be clearly understood.In this wo rk,two electron acceptors,a linear SN6-2Br and a V-shaped BTP-2Br,are developed with nitrogen atoms introduced to replace the traditional sp3-hybridized carbon in the fused ring.BTP-2Br possesses an electron-de ficient central core,which exhibits slightly blue-shifted absorption as well as deepened HOMO-level compared with SN6-2Br.The corresponding photovoltaic performance from V-shaped BTP-2Br based devices exhibit superior performance especially in short-circuit current(Jsc),despite an enhanced absorption and charge carrier mobilities for SN6-2Br.The primary reason for the higher JSC from BTP-2Br is faster exciton diffusion and dissociation in ble nds,than those of SN6-2Br.As a result,PBDB-TF:BTP-2Br based devices achieve a power conversion efficiency(PCE)of 13.84%with an voltage-loss of only 0.46 V,which is one of the lowest values ever reported.Moreover,we fabricated semitransparent OSCs that exhibit an excellent PCE of 9.62%with average visible transparency of 20.1%. 展开更多
关键词 Organic solar cells High efficiency Low voltage-loss Semitransparent OSCs Electron-defficient central core
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