http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Delong Hou,Songhang Wang,Jinming Chang,Zhou Xu,Qi Zeng,Zhonghui Wang,Yongcheng Yang,Jun Yan,Yi Chen 한국섬유공학회 2020 Fibers and polymers Vol.21 No.8
Plasticizers that enable flexible polyvinyl chloride (PVC) are usually combustible, restricting the application ofPVC in fire-prone scenarios. In this context, intrinsically flame-retardant plasticizers displaying dual function continue to bethe focus of intensive research. Despite their efficiency, the majority of these dual-functional plasticizers previously reportedcontain halogen elements, which, once ignited, emanate toxic and potentially carcinogenic substances, along with toxic gasesand smoke, polluting the environment, damaging the biota, and threatening human health. Here, we report a strategy to obtaina halogen-free, intrinsically flame-retardant PVC bio-plasticizer that harnesses the phenolic hydroxyl of naturally occurringcardanol and covalent attachment of an organophosphate moiety. When combined with di-(2-ethylhexyl) phthalate (DOP),the organophosphate-containing cardanol is qualified as a co-plasticizer, while endowing the PVC materials with flameretardancy. Unlike inorganic flame-retardants, the engineered cardanol is compatible with PVC such that the mechanicalproperties of the PVC materials are not compromised. The rationale underlying the present effort may provide guidance fordeveloping sustainable alternatives to halogen-containing plasticizers to address the sustainability challenge now confrontingPVC industry.
Liu, Delong,Yang, Bei,Jang, Bomee,Xu, Bowei,Zhang, Shaoqing,He, Chang,Woo, Han Young,Hou, Jianhui The Royal Society of Chemistry 2017 ENERGY AND ENVIRONMENTAL SCIENCE Vol.10 No.2
<P>Two p-type conjugated polymers with disparate optical and electronic properties, PB3T and PB2T, were developed and applied in fullerene-free polymer solar cells (PSCs). The photovoltaic performance of the PB3T-based PSC device processed by anisole achieved a high power conversion efficiency of 11.9% with a <I>J</I>sc of 18.8 mA cm<SUP>−2</SUP> and <I>V</I>oc of 1.00 V.</P>
Zhang, Shaoqing,Qin, Yunpeng,Uddin, Mohammad Afsar,Jang, Bomee,Zhao, Wenchao,Liu, Delong,Woo, Han Young,Hou, Jianhui American Chemical Society 2016 Macromolecules Vol.49 No.8
<P>Here, taking a polythiophene derivative (PBDD4T) as a starting polymer, we tried to increase the rotation barrier and hence stabilize its backbone conformation by introducing fluorine into the beta and beta'-position of the alpha-linked bithiophene segments and then synthesized a new polymer named as PBDD4T-2F. Our results demonstrate that the rotation barrier between the a-linked bithiophene significantly increases after the fluorination, so PBDD4T-2F has a more stable backbone conformation than PBDD4T. Compared to PBDD4T, PBDD4T-2F shows stronger aggregation effect in solution state and more compact pi-pi stacking in solid thin film and also possesses deeper HOMO level. These properties make PBDD4T-2F being an ideal donor material in PSCs. When blended with PC71BM, a fullerene acceptor, the PBDD4T-2F-based device showed a power conversion efficiency (PCE) of 9.04%, which is 38% higher than that of the PBDD4T-based device; when blended with ITIC, a non-fullerene acceptor, the PBDD4T-2F-based device showed a PCE of 8.69%, which is almost 20 times higher than that of the PBDD4T-based device. What is more, the tandem cell, in which the blend of PBDD4T-2F:PC61BM was used for making the front subcell, exhibited a high PCE of 10.12%. The photovoltaic results indicate that the fluorination is an effective method to enhance interchain pi-pi interaction for the polythiophene and hence to tune its photovoltaic properties in PSCs, especially for the fullerene-free device based on ITIC.</P>