中国科学技术大学学报
中國科學技術大學學報
중국과학기술대학학보
JOURNAL OF UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA
2014年
8期
623-637
,共15页
谢丽欣%赵雪梅%赵志强%甄杰明%陈木青%朱俊%戴松元%杨上峰
謝麗訢%趙雪梅%趙誌彊%甄傑明%陳木青%硃俊%戴鬆元%楊上峰
사려흔%조설매%조지강%견걸명%진목청%주준%대송원%양상봉
聚合物太阳能电池%富勒烯%功能化%3-乙基绕丹宁%6 ,6-苯基-C61-丁酸甲酯(PCBM )
聚閤物太暘能電池%富勒烯%功能化%3-乙基繞丹寧%6 ,6-苯基-C61-丁痠甲酯(PCBM )
취합물태양능전지%부륵희%공능화%3-을기요단저%6 ,6-분기-C61-정산갑지(PCBM )
polymer solar cell%fullerene%functionalization%3-ethyl rhodanine%(6,6)-phenyl-C61 butyric acid methyl ester(PCBM)
首次将染料分子3-乙基绕丹宁连接到[6,6]-苯基-C61-丁酸甲酯(PCBM)上,合成了具有增强光吸收性能的新型富勒烯受体光伏材料PCBRh.通过1HNMR,13CNMR和质谱分析确定了PCBRh的结构,紫外-可见吸收光谱测试表明所合成的PCBRh在300~600nm比起PCBM具有更强的光吸收,这归因于3-乙基绕丹宁高的吸光系数.电化学测试表明PCBRh的最低未占轨道(LUMO)能级比PCBM高0.1eV,这是由绕丹宁基团的给电子作用引起的.将PCBRh作为受体光伏材料与聚己基噻吩(P3HT)共混构建出体相异质结太阳能电池,在优化的制备工艺(P3HT/PCBRh=1:1(质量比),135℃热处理10min)下,电池器件的能量转换效率为1.46%.通过AFM表征研究退火处理对光活性层的形貌的影响及其与电池器件效率的联系:与参比P3HT:PCBM共混薄膜相比,退火处理使P3HT:PCBRh薄膜中的P3HT聚集成长度约为20nm的长条,并且粗糙度较大,因此不利于激子的扩散与分离.
首次將染料分子3-乙基繞丹寧連接到[6,6]-苯基-C61-丁痠甲酯(PCBM)上,閤成瞭具有增彊光吸收性能的新型富勒烯受體光伏材料PCBRh.通過1HNMR,13CNMR和質譜分析確定瞭PCBRh的結構,紫外-可見吸收光譜測試錶明所閤成的PCBRh在300~600nm比起PCBM具有更彊的光吸收,這歸因于3-乙基繞丹寧高的吸光繫數.電化學測試錶明PCBRh的最低未佔軌道(LUMO)能級比PCBM高0.1eV,這是由繞丹寧基糰的給電子作用引起的.將PCBRh作為受體光伏材料與聚己基噻吩(P3HT)共混構建齣體相異質結太暘能電池,在優化的製備工藝(P3HT/PCBRh=1:1(質量比),135℃熱處理10min)下,電池器件的能量轉換效率為1.46%.通過AFM錶徵研究退火處理對光活性層的形貌的影響及其與電池器件效率的聯繫:與參比P3HT:PCBM共混薄膜相比,退火處理使P3HT:PCBRh薄膜中的P3HT聚集成長度約為20nm的長條,併且粗糙度較大,因此不利于激子的擴散與分離.
수차장염료분자3-을기요단저련접도[6,6]-분기-C61-정산갑지(PCBM)상,합성료구유증강광흡수성능적신형부륵희수체광복재료PCBRh.통과1HNMR,13CNMR화질보분석학정료PCBRh적결구,자외-가견흡수광보측시표명소합성적PCBRh재300~600nm비기PCBM구유경강적광흡수,저귀인우3-을기요단저고적흡광계수.전화학측시표명PCBRh적최저미점궤도(LUMO)능급비PCBM고0.1eV,저시유요단저기단적급전자작용인기적.장PCBRh작위수체광복재료여취기기새분(P3HT)공혼구건출체상이질결태양능전지,재우화적제비공예(P3HT/PCBRh=1:1(질량비),135℃열처리10min)하,전지기건적능량전환효솔위1.46%.통과AFM표정연구퇴화처리대광활성층적형모적영향급기여전지기건효솔적련계:여삼비P3HT:PCBM공혼박막상비,퇴화처리사P3HT:PCBRh박막중적P3HT취집성장도약위20nm적장조,병차조조도교대,인차불리우격자적확산여분리.
A dye unit ,3-ethyl rhodanine ,was attached onto (6 ,6)-phenyl-C61 butyric acid methyl ester (PCBM ) for the first time ,affording a new fullerene acceptor PCBM-rhodanine (PCBRh) for polymer solar cells (PSCs) with enhanced light absorption .The successful attachment of the rhodanine moiety was confirmed by 1 H NMR ,13 C NMR and matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF ) mass spectroscopies . UV-vis spectroscopic study indicated that PCBRh had stronger absorptions in the region of 300~600 nm than PCBM ,and this was due to the high absorption coefficient of the dye unit of 3-ethyl rhodanine . Cyclic voltammetric measurement revealed that the lowest unoccupied molecular orbital (LUMO) level of PCBRh was 0 .1 eV higher than that of PCBM ,which can be understood by considering the electron donating property of the rhodanine moiety .Using PCBRh as an acceptor blending with poly(3-hexylthiophene-2 ,5-diyl) (P3HT) ,the bulk heterojunction (BHJ) PSC device exhibited a power conversion efficiency (PCE) of 1.46% under the optimized condition (blending ratio of P3HT :PCBM = 1 :1 (mass ratio ) ,annealing treatment at 135 ℃ for 10 min) . The effect of annealing on the morphology of P3HT :PCBRh active layer and its correlation with the device performance were studied by atomic force microscopy (AFM ) , revealing that in the annealed P3HT :PCBRh blend film P3HT aggregated to long stripes with an average length of ca .20 nm and the RMS roughness increased compared to that for the reference P3HT :PCBM blend film , thus leading to unfavorable exciton diffusion and dissociation .