journal article·2013-10

25th Anniversary Article: No Assembly Required: Recent Advances in Fully Conjugated Block Copolymers

Maxwell J. Robb, Sung‐Yu Ku, Craig J. Hawker

Advanced Materials· Volume 25· Issue 40
Publisher page

Abstract

Fully conjugated block copolymers have emerged as promising materials that combine semiconducting properties with the ability to self‐assemble at the nanoscale. The convergence of these two features has tremendous implications for a number of fundamental molecular assembly and transport questions, while also offering unique advantages for a variety of applications. For example, a nanostructured active layer in organic photovoltaic (OPV) devices may provide for efficient charge separation while simultaneously affording continuous, unimpeded pathways for charge carriers to migrate to their respective electrodes within each individual microphase. This review details the recent progress made in the preparation and application of fully conjugated block copolymers and serves as a comprehensive reference for the materials that have been reported in the literature to date. Focus is placed on fully conjugated block copolymers prepared using chemistries that are relevant to high‐performance polymers in organic electronics research, for example Stille, Suzuki–Miyaura, and Yamamoto coupling.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Block Copolymer Self-Assembly

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Materials Department, Materials Research Laboratory, Department of Chemistry and Biochemistry, Mitsubishi Chemical Center for Advanced Materials University of California Santa Barbara Santa Barbara CA 93106 USA

References (68)

Show source-provided references
1. 10.1146/annurev.pc.41.100190.00252110.1146/annurev.pc.41.100190.002521 ↗
2. 10.1021/ma951138i10.1021/ma951138i ↗
3. 10.1021/ma901350w10.1021/ma901350w ↗
4. 10.1039/c1sm06147j10.1039/c1sm06147j ↗
5. 10.1016/j.progpolymsci.2012.10.00110.1016/j.progpolymsci.2012.10.001 ↗
6. 10.1103/PhysRevLett.39.109810.1103/PhysRevLett.39.1098 ↗
7. 10.1039/c3977000057810.1039/c39770000578 ↗
8. 10.1073/pnas.01258139910.1073/pnas.012581399 ↗
9. 10.1002/anie.20080545610.1002/anie.200805456 ↗
10. 10.1126/science.283.5400.37210.1126/science.283.5400.372 ↗
11. 10.1063/1.164972910.1063/1.1649729 ↗
12. 10.1021/ja073399110.1021/ja0733991 ↗
13. 10.1016/j.progpolymsci.2010.07.00810.1016/j.progpolymsci.2010.07.008 ↗
14. 10.1002/marc.20090008810.1002/marc.200900088 ↗
15. 10.1021/cm049654n10.1021/cm049654n ↗
16. 10.1002/1521-3765(20020715)8:14<3246::AID-CHEM3246>3.0.CO;2-H10.1002/1521-3765(20020715)8:14<3246::AID-CHEM3246>3.0.CO;2-H ↗
17. 10.1039/b702271a10.1039/b702271a ↗
18. 10.1021/ar700253910.1021/ar7002539 ↗
19. 10.1021/ma035706310.1021/ma0357063 ↗
20. 10.1021/ja055688010.1021/ja0556880 ↗
21. 10.1002/marc.20040028110.1002/marc.200400281 ↗
22. 10.1021/ma021362p10.1021/ma021362p ↗
23. 10.1002/adma.20040013710.1002/adma.200400137 ↗
24. 10.1246/cl.2008.102210.1246/cl.2008.1022 ↗
25. 10.1016/j.polymer.2009.11.00110.1016/j.polymer.2009.11.001 ↗
26. 10.1021/ma100519g10.1021/ma100519g ↗
27. 10.1021/ma201024z10.1021/ma201024z ↗
28. 10.1021/ma300013e10.1021/ma300013e ↗
29. 10.1039/c1jm11518a10.1039/c1jm11518a ↗
30. 10.1002/marc.20110031610.1002/marc.201100316 ↗
31. 10.1039/c1py00171j10.1039/c1py00171j ↗
32. 10.1039/C1PY00453K10.1039/C1PY00453K ↗
33. 10.1002/pola.2653110.1002/pola.26531 ↗
34. 10.1021/cm102185510.1021/cm1021855 ↗
35. 10.1021/cm102419z10.1021/cm102419z ↗
36. 10.1021/ar200244610.1021/ar2002446 ↗
37. 10.1021/cr900182s10.1021/cr900182s ↗
38. 10.1007/s00289007000410.1007/s002890070004 ↗
39. 10.1007/s00289017005910.1007/s002890170059 ↗
40. 10.1002/marc.20120073410.1002/marc.201200734 ↗
41. 10.1021/nl202691n10.1021/nl202691n ↗
42. 10.1021/ma102728z10.1021/ma102728z ↗
43. 10.1002/smll.20060035110.1002/smll.200600351 ↗
44. 10.1021/ma702402g10.1021/ma702402g ↗
45. 10.1039/B918583F10.1039/B918583F ↗
46. 10.1021/la903520w10.1021/la903520w ↗
47. 10.1016/j.polymer.2010.03.01010.1016/j.polymer.2010.03.010 ↗
48. 10.1021/ja203767310.1021/ja2037673 ↗
49. 10.1002/adma.20120281710.1002/adma.201202817 ↗
50. 10.1021/ma202738t10.1021/ma202738t ↗
51. 10.1002/marc.20110003710.1002/marc.201100037 ↗
52. 10.1021/nl401420s10.1021/nl401420s ↗
53. 10.1039/C2PY20830J10.1039/C2PY20830J ↗
54. 10.1021/ma300533k10.1021/ma300533k ↗
55. 10.1021/jp201344p10.1021/jp201344p ↗
56. 10.1021/ja307431k10.1021/ja307431k ↗
57. 10.1002/pola.2200310.1002/pola.22003 ↗
58. 10.1002/1521-3927(20010501)22:8<624::AID-MARC624>3.0.CO;2-310.1002/1521-3927(20010501)22:8<624::AID-MARC624>3.0.CO;2-3 ↗
59. 10.1021/mz400143y10.1021/mz400143y ↗
60. 10.1021/ma200084z10.1021/ma200084z ↗
61. 10.1021/ma802587f10.1021/ma802587f ↗
62. 10.1021/cm102154q10.1021/cm102154q ↗
63. Stille coupling also generates a stoichiometric quantity of organotin byproducts which are a concern for purity and environmental reasons.
64. 10.1016/S0040-6090(02)00635-110.1016/S0040-6090(02)00635-1 ↗
65. 10.1002/1521-4095(20020404)14:7<477::AID-ADMA477>3.0.CO;2-910.1002/1521-4095(20020404)14:7<477::AID-ADMA477>3.0.CO;2-9 ↗
66. 10.1021/ma302170e10.1021/ma302170e ↗
67. 10.1021/ma102566u10.1021/ma102566u ↗
68. 10.1021/ma060341i10.1021/ma060341i ↗