2015
DOI: 10.1038/nphoton.2015.6
|View full text |Cite
|
Sign up to set email alerts
|

Single-junction polymer solar cells with high efficiency and photovoltage

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

26
1,111
0
6

Year Published

2015
2015
2022
2022

Publication Types

Select...
6
4

Relationship

0
10

Authors

Journals

citations
Cited by 1,612 publications
(1,143 citation statements)
references
References 29 publications
26
1,111
0
6
Order By: Relevance
“…It yielded a capacity of 150 mAhg -1 which drops to 18 mAhg -1 after 40 cycles. Similarly, tri-carbonyl-based tris-N-salicylideneanthramine(TSAA) and tris-N-salicylideneanthraquinoylamine (TSAQ) showed excellent reversible transformation between C=O and C-O-Na because the reactivity of the α-carbon radical intermediates was largely suppressed by an electronic resonance effect and steric hindrance from the substitution groups [60]. TSAQ delivered capacities of 370 and 220 mAhg -1 at 50 mAg -1 and 1 Ag -1 , respectively, and showed no obvious capacity degradation after more than 2500 cycles at 1 Ag -1 .…”
Section: Ketonesmentioning
confidence: 99%
“…It yielded a capacity of 150 mAhg -1 which drops to 18 mAhg -1 after 40 cycles. Similarly, tri-carbonyl-based tris-N-salicylideneanthramine(TSAA) and tris-N-salicylideneanthraquinoylamine (TSAQ) showed excellent reversible transformation between C=O and C-O-Na because the reactivity of the α-carbon radical intermediates was largely suppressed by an electronic resonance effect and steric hindrance from the substitution groups [60]. TSAQ delivered capacities of 370 and 220 mAhg -1 at 50 mAg -1 and 1 Ag -1 , respectively, and showed no obvious capacity degradation after more than 2500 cycles at 1 Ag -1 .…”
Section: Ketonesmentioning
confidence: 99%
“…Over the last 15 years, organic photovoltaics have experienced slow but sustained progress. 1 From the earliest poly( p-phenylene vinylene) devices (with the low 3% power conversion efficiency (PCE)) [2][3][4] to the poly(3-hexylthiophene-2,5-diyl) devices (with 5% PCE) [5][6][7] and the state-of-the-art donoracceptor (D-A) photovoltaic devices (with 11% PCE), [8][9][10][11][12] the most common feature of these materials is their polymeric nature. However, Q6…”
Section: Q5mentioning
confidence: 99%
“…Great progress has been achieved in both donor and acceptor materials development and device optimization, witnessed by the dramatic increase in devices PCEs from less than 2% before 2008 to over than 10% in recent years [11][12][13][14][15]. In this regard, fullerene and their derivatives have been extensively used as acceptor materials within BHJ devices because of their important electronic properties such as small reorganization energy, high electron mobility and affinity [16][17][18].…”
Section: Introductionmentioning
confidence: 99%