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π-Extension and chlorination of non-fullerene acceptors enable more readily processable and sustainable high-performance organic solar cells
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作者 Ning Su Jianhua Chen +6 位作者 Mengran Peng Guoping Li Robert M.Pankow Ding Zheng Junqiao Ding Antonio Facchetti Tobin J.Marks 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2023年第4期321-329,共9页
Organic solar cells(OSCs)processed without halogenated solvents and complex treatments are essential for future commercialization.Herein,we report three novel small molecule acceptors(NFAs)consisting of a Y6-like core... Organic solar cells(OSCs)processed without halogenated solvents and complex treatments are essential for future commercialization.Herein,we report three novel small molecule acceptors(NFAs)consisting of a Y6-like core but withπ-extended naphthalene with progressively more chlorinated end-capping groups and a longer branched chain on the Nitrogen atom.These NFAs exhibit good solubilities in nonchlorinated organic solvents,broad optical absorptions,closeπ-πstacking distances(3.63–3.84A),and high electron mobilities(~10^(-3)cm^(2)V^(-1)s^(-1)).The o-xylene processed and as-cast binary devices using PM6 as the donor polymer exhibit a PCE increasing upon progressive chlorination of the naphthalene end-capping group from 8.93%for YN to 14.38%for YN-Cl to 15.00%for YN-2Cl.Furthermore similarly processed ternary OSCs were fabricated by employing YN-Cl and YN-2Cl as the third component of PM6:CH1007 blends(PCE=15.75%).Compared to all binary devices,the ternary PM6:CH1007:YN-Cl(1:1:0.2)and PM6:CH1007:YN-2Cl(1:1:0.2)cells exhibit significantly improved PCEs of 16.49%and15.88%,respectively,which are among the highest values reported to date for non-halogenated solvent processed OSCs without using any additives and blend post-deposition treatments. 展开更多
关键词 Non-fullerene acceptors Non-chlorinated organic solvents organic solar cells
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Investigation on Organic Solvent Free Toluene Oxidative Bromination Reaction Catalyzed by HTS Zeolite 被引量:2
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作者 Peng Xinxin Xia Changjiu +3 位作者 Lin Min Zhu Bin Luo Yibin Shu Xingtian 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2020年第4期1-9,共9页
The toluene oxidative bromination reaction catalyzed by hollow titanium silicalite(HTS)zeolite in aqueous medium was investigated by employing H2O2 and HBr under mild conditions without the need for organic solvent.A ... The toluene oxidative bromination reaction catalyzed by hollow titanium silicalite(HTS)zeolite in aqueous medium was investigated by employing H2O2 and HBr under mild conditions without the need for organic solvent.A high toluene conversion(90.7%)and high selectivity of mono-bromotoluene(99.0%)was achieved under the optimal reaction conditions.The UV-Raman spectroscopy was applied for the mechanism study and the result reveals that HTS is efficient for catalyzing the oxidation reaction of HBr with H2O2 to produce abundant active bromine species,which can further facilitate the toluene electrophilic bromination reaction.A two-step toluene bromination reaction mechanism involving the HTS catalyzed active bromine species“generation-conversion-utilization”process is proposed based on the UV-Raman spectroscopy analysis. 展开更多
关键词 titanium silicalite oxidative bromination organic solvent free H2O2/HBr polybromine ion
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CO_2 selective hydrogenation to synthetic natural gas(SNG) over four nano-sized Ni/ZrO_2 samples:ZrO_2 crystalline phase & treatment impact 被引量:3
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作者 Min Chen Zhanglong Guo +2 位作者 Jian Zheng Fangli Jing Wei Chu 《Journal of Energy Chemistry》 SCIE EI CAS CSCD 2016年第6期1070-1077,共8页
Two type zirconia (monoclinic and tetragonal phase ZrO2) carriers were synthesized via hydrothermal route, and nano-sized zirconia supported nickel catalysts were prepared by incipient impregnation then followed therm... Two type zirconia (monoclinic and tetragonal phase ZrO2) carriers were synthesized via hydrothermal route, and nano-sized zirconia supported nickel catalysts were prepared by incipient impregnation then followed thermal treatment at 300 °C to 500 °C, for the CO2selective hydrogenation to synthetic natural gas (SNG). The catalysts were characterized by XRD, CO2-TPD-MS, XPS, TPSR (CH4, CO2) techniques. For comparison, the catalyst NZ-W-400 (monoclinic) synthesized in water solvent exhibited a better catalytic activity than the catalyst NZ-M-400 (tetragonal) prepared in methanol solvent. The catalyst NZ-W-400 displayed more H2absorbed sites, more basic sites and a lower temperature of initial CO2activation. Then, the thermal treatment of monoclinic ZrO2supported nickel precursor was manufactured at three temperature of 350, 400, 500 °C. The TPSR experiments displayed that there were the lower temperature for CO2activation and initial conversion (185 °C) as well as the lower peak temperature of CH4generation (318 °C), for the catalyst calcined at 500 °C. This sample contained the more basic sites and the higher catalytic activity, evidenced byCO2-TPD-MS and performance measurement. As for the NZ-W-350 sample, which exhibited the less basic sites and the lower catalytic activity, its initial temperature for CO2activation and conversion was higher (214 °C) as well as the higher peak temperature of CH4formation (382 °C). © 2016 Science Press 展开更多
关键词 Carbon dioxide Catalyst activity Catalysts Chemical activation Heat treatment HYDROGENATION Natural gas Nickel organic solvents ZIRCONIA Zirconium alloys
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Organic solvent nanofiltration membranes for separation in non-polar solvent system
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作者 Shuyun Gu Siyao Li Zhi Xu 《Green Energy & Environment》 2025年第2期244-267,共24页
Membrane technology holds significant potential for augmenting or partially substituting conventional separation techniques,such as heatdriven distillation,thereby reducing energy consumption.Organic solvent nanofiltr... Membrane technology holds significant potential for augmenting or partially substituting conventional separation techniques,such as heatdriven distillation,thereby reducing energy consumption.Organic solvent nanofiltration represents an advanced membrane separation technology capable of discerning molecules within a molecular weight range of approximately 100-1000 Da in organic solvents,offering low energy requirements and minimal carbon footprints.Molecular separation in non-polar solvent system,such as toluene,n-hexane,and n-heptane,has gained paramount importance due to their extensive use in the pharmaceutical,biochemical,and petrochemical industries.In this review,we presented recent advancements in membrane materials,membrane fabrication techniques and their promising applications for separation in nonpolar solvent system,encompassing hydrocarbon separation,bioactive molecule purification and organic solvent recovery.Furthermore,this review highlighted the challenges and opportunities associated with membrane scale-up strategies and the direct translation of this promising technology into industrial applications. 展开更多
关键词 organic solvent nanofiltration Membranes Membrane separation Non-polar solvent system Petrochemical and pharmaceutical application
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