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Supporting Information for Bombyx mori silk/titania/gold hybrid materials for photocatalytic water splitting: combining renewable raw materials with clean fuels Stefanie Krüger 1, Michael Schwarze 2, Otto Baumann 3, Christina Günter 4, Michael Bruns 5, Christian Kübel 6, Dorothée Vinga Szabó 5, Rafael Meinusch 7, Verónica de Zea Bermudez 8 and Andreas Taubert* 1, Address: 1 Institute of Chemistry, University of Potsdam, D-14476 Potsdam, Germany, 2 Institute of Chemistry, Technical University Berlin, D-10623 Berlin, Germany, 3 Institute of Biochemistry and Biology, University of Potsdam, D-14476 Potsdam, Germany, 4 Institute of Earth and Environmental Science, University of Potsdam, D-14476 Potsdam, Germany, 5 Institute for Applied Materials (IAM) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT), D-76344 Eggenstein-Leopoldshafen, Germany, 6 Institute of Nanotechnology (INT) and Karlsruhe Nano Micro Facility (KNMF), Karlsruhe Institute of Technology (KIT), D-76344 Eggenstein-Leopoldshafen, Germany, 7 Institute of Physical Chemistry, Justus-Liebig-University Giessen, D-35392 Giessen, Germany and 8 Department of Chemistry and CQ-VR, University of Trás-os-Montes e Alto Douro, Pt-5001-801 Vila Real, Portugal Email: Andreas Taubert - ataubert@uni-potsdam.de * Corresponding author Tel.: +49 (0) 331 977 5773 Additional data S1

Table S1: Hybrid materials studied in this work. Note that only the main components are given. For details of sample preparation and composition see experimental section below. TS TS_Au x TPS TPS_Au x m (PEO 780 ) (mg) - - 200 200 m (PEO 8300 ) (mg) - - 200 200 m (Silk in silk solution) (mg) 800 800 400 400 V (Ti(OiPr) 4 ) (ml) 5.0 5.0 5.0 5.0 m (HAuCl 4 3H 2 O) (mg) - 2.5 5.6 6.1-1.0 2.5 5.0 10.7 Figure S1: Digital microscopy images of TPS_Au 2.5 and TS_Au 2.5. Top surface of the material is on the left hand side of both images. S2

Figure S2: TEM image of TPS with a larger pore of around 50 µm (bottom of image). Figure S3: Dark field STEM (DF-STEM) image of TS_Au 5.0 and TPS_Au 2.5. The light spots are the AuNP, the gray background is the titania/silk hybrid and black areas are holes or regions with very little material. S3

Figure S4: HRTEM images of TS_Au 5.0 and TPS_Au 2.5 along with the corresponding FFT images and EDX spectra. The copper signals stem from stray signals from the Cu-TEM grid. Carbon and oxygen signals may originate from TiO 2, the surrounding silk, and/or embedding resin. S4

Table S2: Lattice spacings and corresponding hkl index assignments of the FFT evaluated using PASAD [1]. measured anatase brookite Au TS_Au 5.0 [ICDD 98-015-4602] [ICDD 00-029-1360] [ICDD 00-004-0784] K [1/nm] d [nm] hkl d [nm] hkl d [nm] hkl d [nm] 2.821 0.354 011 0.353 120 0.351 3.501 0.286 121 0.290 4.231 0.236 004 0.237 131 0.237 111 0.236 5.238 0.191 020 0.190 231 0.189 5.871 0.170 015 0.170 320 0.169 4.179 a 0.239 111 0.236 4.937 a 0.203 200 0.204 measured anatase brookite Au TPS_Au 2.5 [ICDD 98-015-4602] [ICDD 00-029-1360] [ICDD 00-004-0784] K [1/nm] d [nm] hkl d [nm] hkl d [nm] hkl d [nm] 2.868 0.349 011 0.353 120 0.351 4.693 0.213 221 0.213 5.162 0.194 020 0.190 032 0.197 5.930 0.169 015 0.170 320 0.169 4.166 a 0.240 111 0.236 4.937 a 0.203 200 0.204 a Reflections measured directly on the particle. S5

Figure S5: a) XRD pattern of TPS_Au 5.0 highlighting the region between 35-47. b) XRD patterns of a wet (red line) and dry (black line) TPS hybrid material. S6

Table S3: XPS binding energies, assignments to the respective binding partners, and atomic concentrations for the samples TS_Au 2.5 and TPS_Au 2.5. TPS_Au 2.5 [atom %] TS_Au 2.5 [atom %] Peak Binding energy Atomic Atomic Assignment [ev] a Concentration [%] Concentration [%] Au 4f 7/2 84.0 1.2 2.2 Au 0 [2] C 1s 285.0 16.2 23.9 C-C/ C-H [3-6] 286.4 21.0 20.2 C-N/ C-O [3-7] 288.3 16.7 16.4 O=C-N/ O=C-OH [3-5,7] N 1s 400.1 16.8 16.4 C-N-H/ O=C-N [6-9] 402.0 0.5 0.6 C-N + H x [3] Ti 2p 3/2 459.0 2.1 0.2 TiO 2 [10] Ti-O-C [11] O 1s 530.5 4.7 - TiO 2 [10] 531.8 16.9 17.0 O=C-N/ O=C [3,6] Ti-OH [12] 533.3 3.5 3.2 C-O [3,6] Ti-OH [12] a The binding energies are referenced to the C 1s = 285.0 ev energy of hydrocarbons. In consequence the uncertainty for weak peaks (even for Au 4f 7/2 ) is ±0.2 ev. S7

Figure S6: XPS sputter depth profiles of the TPS_Au 2.5 surface (top) and a zoom in (bottom). Note: as it was not possible to determine the sample thickness [13], the data are represented vs. sputter time. Table S4: Chemical composition of the hybrid materials obtained from EA. sample C ± 0.3 % H ± 0.3 % N ± 0.3 % total amount CHN TiO 2 a 1.5 1.2 0 2.7 silk 46.2 7.2 17.9 71.3 TPS 9.5 2.4 3.4 15.2 TPS_Au 2.5 9.1 2.3 3.3 14.6 TS 13.3 2.9 4.9 21.2 TS_Au 2.5 13.2 2.8 4.9 20.8 a The CHN amount in TiO 2 comes from unreacted Ti(OiPr) 4 and EtAcAc. S8

Figure S7: TGA curves of TiO 2 (black line) TPS (red line), TPS_Au 2.5 (light blue line), TS (violet line), TS_Au 2.5 (green line) and B. mori silk (dark blue line). Figure S8: H 2 production of TPS_Au 5.8 using a sunlight simulator or a xenon lamp. A possible mechanism for water splitting in the presence of ethanol in shown in Equation S1 S5 (adapted by Chen et al. [14]) TiO 2 + hν h + + e - H 2 O + h + OH + H + OH + CH 3 CH 2 OH CH 3 CHOH + H 2 O CH 3 CHOH + OH CH 3 CH(OH) 2 CH 3 CHO + H 2 O (S1) (S2) (S3) (S4) 2 H + + 2 e - H 2 (S5) References 1 C. Gammer, C. Mangler, C. Rentenberger and H. P. Karnthaler, Scr. Mater., 2010, 63, 312 315. 2 Y. Joseph, I. Besnard, M. Rosenberger, B. Guse, H. Nothofer, J. M. Wessels, U. Wild, A. Knop- S9

Gericke, D. Su, R. Schlögl, A. Yasuda and T. Vossmeyer, J. Phys. Chem. B, 2003, 107, 7406 7413. 3 N. Zydziak, C. M. Preuss, V. Winkler, M. Bruns, C. Hübner and C. Barner-Kowollik, Macromol. Rapid Commun., 2013, 34, 672 680. 4 E. H. Lock, D. Y. Petrovykh, P. Mack, T. Carney, R. G. White, S. G. Walton and R. F. Fernsler, Langmuir, 2010, 26, 8857 8868. 5 C. Rodriguez-Emmenegger, C. M. Preuss, B. Yameen, O. Pop-Georgievski, M. Bachmann, J. O. Mueller, M. Bruns, A. S. Goldmann, M. Bastmeyer and C. Barner-Kowollik, Adv. Mater., 2013, 25, 6123 6127. 6 S. Engin, V. Trouillet, C. M. Franz, A. Welle, M. Bruns and D. Wedlich, Langmuir, 2010, 26, 6097 6101. 7 C. M. Preuss, T. Tischer, C. Rodriguez-Emmenegger, M. M. Zieger, M. Bruns, A. S. Goldmann and C. Barner-Kowollik, J. Mater. Chem. B, 2014, 2, 36 40. 8 M. Bruns, C. Barth, P. Brüner, S. Engin, T. Grehl, C. Howell, P. Koelsch, P. MacK, P. Nagel, V. Trouillet, D. Wedlich and R. G. White, Surf. Interface Anal., 2012, 44, 909 913. 9 T. Tischer, A. S. Goldmann, K. Linkert, V. Trouillet, H. G. Börner and C. Barner-Kowollik, Adv. Funct. Mater., 2012, 22, 3853 3864. 10 I. Tunc, M. Bruns, H. Gliemann, M. Grunze and P. Koelsch, Surf. Interface Anal., 2010, 42, 835 841. 11 B. Qiu, Y. Zhou, Y. Ma, X. Yang, W. Sheng, M. Xing and J. Zhang, Sci. Rep., 2015, 5, 8591. 12 J. Yan, G. Wu, N. Guan, L. Li, Z. Li and X. Cao, Phys. Chem. Chem. Phys., 2013, 15, 10978 88. 13 Mai, T.; Wolski, K.; Puciul-Malinowska, A.; Kopyshev, A.; Gräf, R.; Bruns, M.; Zapotoczny, S.; Taubert, A. Anionic Polymer Brushes for Biomimetic Calcium Phosphate Mineralization a Surface with Application Potential in Biomaterials. Biomacromolecules, in press. 14 X. Chen, S. Shen, L. Guo and S. S. Mao, Chem. Rev., 2010, 110, 6503 6570. S10