journal article·2020-12-23

In SituStudy of Order Formation in Mesoporous Titania Thin Films Templated by a Diblock Copolymer during Slot-Die Printing

Nian Li, Wei Chen, Lin Song, Renjun Guo, Manuel A. Scheel, Dan Yang, Volker Körstgens, Matthias Schwartzkopf, Stephan V. Roth, Peter Müller-Buschbaum

ACS Applied Materials & Interfaces· Volume 12· Issue 51
Publisher page

Abstract

Slot-die printing, a large-scale deposition technique, is applied to fabricate mesoporous titania films. Printing is interesting, for example, for scaling up solar cells where titania films with an interconnected mesoporous network and a large surface-to-volume ratio are desired as photoanodes. A fundamental understanding of the structure evolution during printing is of high significance in tailoring these films. In this work, we provide important insights into the self-assembly of the slot-die-printed titania/polystyrene-block-poly(ethylene oxide) (PS-b-PEO) micelles into ordered hybrid structures in real time via in situ grazing-incidence small-angle X-ray scattering (GISAXS). GISAXS allows for tracking both vertical and lateral structure development of the film formation process. In the hybrid film, a face-centered cubic (FCC) structure is preferentially formed at the interfaces with air and with the substrate, while a defect-rich mixed FCC and body-centered cubic (BCC) structure forms in the bulk. After calcination, the surface and inner morphologies of the obtained nanostructured titania films are compared with the spin-coated analogues. In the printed films, the initially formed nanoscale structure of the hybrid film is preserved, and the resulting mesoporous titania film shows a superior order as compared with the spin-coated thin films which can be beneficial for future applications.
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Research context

OpenAlex topics: Electrophoretic Deposition in Materials Science · TiO2 Photocatalysis and Solar Cells · Block Copolymer Self-Assembly

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

Affiliations

Lehrstuhl für Funktionelle Materialien, Physik-Department, Technische Universität München, James-Franck-Str. 1, 85748 Garching, Germany

Institute of Flexible Electronics (IFE), Northwestern Polytechnical University (NPU), Youyixilu 127, Xi’an 710072, Shaanxi, China

Deutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22603 Hamburg, Germany

Department of Fibre and Polymer Technology, KTH Royal Institute of Technology, Teknikringen 56-58, 100 44 Stockholm, Sweden

Heinz Maier-Leibnitz Zentrum (MLZ), Technische Universität München, Lichtenbergstr. 1, 85748 Garching, Germany

Funding

Deutsche Forschungsgemeinschaft · Center for NanoScience, Ludwig-Maximilians-Universit?t M?nchen · Bayerisches Staatsministerium f?r Bildung und Kultus, Wissenschaft und Kunst · China Scholarship Council

References (62)

Show source-provided references
1. 10.1021/nn201243y10.1021/nn201243y ↗
2. 10.1002/ange.20050133710.1002/ange.200501337 ↗
3. 10.1039/C5CY00879D10.1039/C5CY00879D ↗
4. Lan K. · Angew. Chem., Int. Ed. · 2020 · 59 · 210.1002/anie.201914768 ↗
5. 10.1021/ja500873u10.1021/ja500873u ↗
6. 10.1021/nl300173j10.1021/nl300173j ↗
7. 10.1038/nature1106710.1038/nature11067 ↗
8. 10.1038/nphoton.2012.2210.1038/nphoton.2012.22 ↗
9. 10.1038/353737a010.1038/353737a0 ↗
10. 10.1021/cr400625j10.1021/cr400625j ↗
11. 10.1126/science.120968810.1126/science.1209688 ↗
12. 10.1038/ncomms1539010.1038/ncomms15390 ↗
13. 10.1002/adma.20050202310.1002/adma.200502023 ↗
14. Park N. · Adv. Energy Mater. · 2019 · 1
15. 10.1002/adma.20110178310.1002/adma.201101783 ↗
16. 10.1016/j.mtcomm.2019.10072810.1016/j.mtcomm.2019.100728 ↗
17. 10.1021/ma971419l10.1021/ma971419l ↗
18. 10.1016/j.nanoen.2017.05.00810.1016/j.nanoen.2017.05.008 ↗
19. 10.1021/ja056285310.1021/ja0562853 ↗
20. 10.1103/PhysRevLett.71.210210.1103/PhysRevLett.71.2102 ↗
21. 10.1002/adma.20110178310.1002/adma.201101783 ↗
22. 10.1002/ente.20190092210.1002/ente.201900922 ↗
23. 10.1016/j.jcis.2015.11.07010.1016/j.jcis.2015.11.070 ↗
24. 10.1016/j.solmat.2007.11.00910.1016/j.solmat.2007.11.009 ↗
25. Li N. · Adv. Mater. Interfaces · 2019 · 1
26. 10.1016/j.solmat.2008.10.00410.1016/j.solmat.2008.10.004 ↗
27. 10.1088/0953-8984/28/40/40300310.1088/0953-8984/28/40/403003 ↗
28. 10.1002/adma.20140404010.1002/adma.201404040 ↗
29. Pröller S. · Adv. Energy Mater. · 2016 · 6 · 110.1002/aenm.201501580 ↗
30. 10.1039/D0NH00008F10.1039/D0NH00008F ↗
31. 10.1016/j.nanoen.2017.08.02310.1016/j.nanoen.2017.08.023 ↗
32. 10.1021/acsami.7b1485010.1021/acsami.7b14850 ↗
33. 10.1002/smll.20060071210.1002/smll.200600712 ↗
34. 10.1039/C9NR08055D10.1039/C9NR08055D ↗
35. 10.1107/S090904951201689510.1107/S0909049512016895 ↗
36. 10.1021/ma971486f10.1021/ma971486f ↗
37. 10.1021/acsami.9b0657310.1021/acsami.9b06573 ↗
38. 10.1103/PhysRevB.26.414610.1103/PhysRevB.26.4146 ↗
39. 10.1103/PhysRevB.38.229710.1103/PhysRevB.38.2297 ↗
40. 10.1103/PhysRevB.52.1685510.1103/PhysRevB.52.16855 ↗
41. 10.1107/S002188980200608810.1107/S0021889802006088 ↗
42. 10.1039/C6TC02412B10.1039/C6TC02412B ↗
43. 10.1021/jacs.8b1308210.1021/jacs.8b13082 ↗
44. 10.1039/c3sm27589b10.1039/c3sm27589b ↗
45. 10.1021/nn103303q10.1021/nn103303q ↗
46. 10.1021/nl302628910.1021/nl3026289 ↗
47. 10.1002/9781119998365.ch310.1002/9781119998365.ch3 ↗
48. Cao W. · Sci. Rep. · 2019 · 9 · 110.1038/s41598-018-37186-2 ↗
49. 10.1039/C2SM26502H10.1039/C2SM26502H ↗
50. 10.1021/ja304259y10.1021/ja304259y ↗
51. 10.1038/nmat460010.1038/nmat4600 ↗
52. Perlich J. · Rev. Sci. Instrum. · 2010 · 81 · 110.1063/1.3488459 ↗
53. 10.1103/PhysRev.131.201010.1103/PhysRev.131.2010 ↗
54. 10.1039/C5SM02441B10.1039/C5SM02441B ↗
55. 10.1021/ma500633b10.1021/ma500633b ↗
56. 10.1021/jp010944q10.1021/jp010944q ↗
57. 10.1002/adfm.20110038210.1002/adfm.201100382 ↗
58. 10.1103/PhysRevB.59.1419110.1103/PhysRevB.59.14191 ↗
59. 10.1016/j.surfrep.2009.07.00210.1016/j.surfrep.2009.07.002 ↗
60. 10.1007/s00216-003-1869-210.1007/s00216-003-1869-2 ↗
61. 10.1039/C4TA00489B10.1039/C4TA00489B ↗
62. 10.1002/adma.20110064010.1002/adma.201100640 ↗