<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ma, Shengbo</style></author><author><style face="normal" font="default" size="100%">Ting, Hungkit</style></author><author><style face="normal" font="default" size="100%">Zhang, Lipei</style></author><author><style face="normal" font="default" size="100%">Ma, Yingzhuang</style></author><author><style face="normal" font="default" size="100%">Zheng, Lingling</style></author><author><style face="normal" font="default" size="100%">Xiao, Lixin</style></author><author><style face="normal" font="default" size="100%">Chen, Zhijian</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Reversible photoinduced bi-state polymer solar cells based on fullerene derivatives with azobenzene groups</style></title><secondary-title><style face="normal" font="default" size="100%">ORGANIC ELECTRONICS</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2015</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">23</style></volume><pages><style face="normal" font="default" size="100%">1-4</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">[6,6]-Phenyl-C61-butyric acid-4&amp;#039;-hydroxyl-azobenzene ester (PCBAb) was synthesized and used as the acceptor in the fabrication of reversible UV-VIS response bi-state polymer solar cells (PSCs) based on the photoinduced cis-trans isomerization of PCBAb. The device can be switched between ``active&amp;#039;&amp;#039; and ``sleep&amp;#039;&amp;#039; by the irradiation of UV and visible light, respectively. The active device has a PCE of 2.0%. With UV irradiation, the device goes to ``sleep&amp;#039;&amp;#039; with a lowered PCE (0.4%), and simultaneously decreased J(sc), V-oc and FF, while after visible light treatment, the device is made ``active&amp;#039;&amp;#039; again. The mechanism of the bi-state process involves the different electron mobilities of the isomers. (C) 2015 Elsevier B.V. All rights reserved.</style></abstract></record></records></xml>