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Electronic Supplementary Material (ESI) for Journal of Materials Chemistry A. This journal is The Royal Society of Chemistry 018 Electronic Supplementary Information Superhydrophilic amorphous Co-B-P nanosheet electrocatalysts with Pt-like activity and durability for the hydrogen evolution reaction Hongming Sun, a Xiaobin Xu, b Zhenhua Yan, a Xiang Chen, a Lifang Jiao, a Fangyi Cheng,* a Jun Chen a,c a. Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), College of Chemistry, Nankai University, Tianjin 300071. E-mail: fycheng@nankai.edu.cn. b. Department of Chemistry and Biochemistry, University of California, Los Angeles, Los Angeles, CA 90095, USA. c. State Key Laboratory of Elemento-Organic Chemistry, Innovative Collaboration Center of Chemical Science and Engineering, Nankai University, Tianjin 300071, China. 1

Fig. S1 Schematic illustration of the synthesis of Co-B-P supported on Ni foam. Fig. S (a) EDS spectrum and elemental composition (inset) of Co-B-P-/NF. (d) XRD pattern of Co-B-P-/NF. Fig. S3 The wettability test of Co-B-P nanosheet arrays (a) and Co-B-P nanospheres (b) deposited on Ni foil, respectively. To eliminate the influence of the asperous substrate (Ni foam) for the contact angle measurements, the contact angles of Co-B-P nanosheet arrays and Co-B-P nanospheres loaded on Ni foil were also tested. The results indicate that Co-B-P nanosheet arrays on Ni foil is also hydrophilic, while contact angle between water and the Co-B-P

nanospheres on Ni foil is measured to be 105.0, showing non-hydrophilic (Video S1). The result is consistent with that of Co-B-P/NF and Co-B-P-/NF (Fig. 1c,f insets). Fig. S4 (a, b) TEM images of Co-B-P/NF. Fig. S5 XRD patterns of Co-P/NF, Co-B-P/NF and Co-B/NF. 3

Fig.S6 SEM images, SEM-EDS spectroscopies and elemental composition analysis of (a-c) Co-B-P/NF-1, (d-f) Co-B- P/NF-, (g-i) Co-B-P/NF-3, (j-l) Co-B-P/NF-4. The elemental compositions of Co-B-P/NF-1, Co-B-P/NF-, Co-B-P/NF-3 and Co-B-P/NF-4 from EDS analysis were Co.80 B0.68P0.3, Co.77B0.8P0.18, Co.95B0.87P0.13 and Co3.03B0.94P0.06, respectively. Fig. S7 (a) Low- and (b) high-magnification SEM images of Co-B/NF. (c) SEM image and EDS elemental mapping of Co and B. (d) The corresponding EDS spectrum and elemental composition analysis (inset). 4

Fig. S8 (a) Low- and (b) high-magnification SEM images of Co-P/NF. (c) SEM image and elemental mapping of Co and P. (d) The corresponding EDS spectrum and elemental composition analysis (inset). Fig.S9 (a) Polarization curves of Co-B-P/NF-1, Co-B-P/NF, Co-B-P/NF-, Co-B-P/NF-3 and Co-B-P/NF-4 in 1 M KOH electrolyte. (b) Tafel plots derived from (a). (c) Comparison of the overpotentials at 10 ma cm and Tafel slopes of the Co-B-P/NF-1, Co-B-P/NF, Co-B-P/NF-, Co-B-P/NF-3 and Co-B-P/NF-4. 5

Fig. S10 (a) Original and ir-corrected polarization curves of Co-B-P/NF, Co-P/NF and Co-B/NF. (b) EIS Nyquist plots of Ni Foam, Co-B/NF, Co-P/NF, Co-B-P/NF and Pt/C recorded at overpotential of 100 mv. Fig. S11 CV curves recorded at different scan rates between 0.10 and 0.17 V for (a) Ni foam, (b) Co-B/NF, (c) Co-B- P/NF and (d) Co-P/NF. 6

Fig. S1 Capacitive currents on the basis of scan rate for Ni foam, Co-B/NF, Co-P/NF and Co-B-P/NF at 0.135 V. Calculation of electrochemically active surface area (): The was determined assuming a Cdl capacitance ( mf cm ) of Ni foam (Fig. S11), which was used as the substrate and considered as the reference. s1 A Co-B/NF = - 43.8 mfcm - mf cm per cm = 1.9 cm A Co-B-P/NF = - 55 mf cm - mf cm per cm = 7.5 cm A Co-P/NF = - 46.6 mfcm - mf cm per cm = 3.3 cm Fig. S13 (a) Polarization curves of Co-B/NF in 1 M KOH solution with or without 10 mm KSCN. (b) Polarization curves of Co-P/NF in 1 M KOH solution with or without 10 mm KSCN. 7

Fig.S14 The XRD patterns of Co-B-P/NF after thermal treatment at different temperatures for h. Fig. S15 The polarization curves of Co-B-P/NF after thermal treatment at different temperatures. Fig. S16 (a) CV curves recorded at different scan rates between 0.10 and 0.17 V for Co-B-P-/NF. (b) Capacitive currents on the basis of scan rate for Co-B-P-/NF. Calculation of is given below: 8

A Co-B-P-/NF = - 34 mf cm - mf cm per cm = 17.0 cm Fig. S17 -normalized initial polarization curves from Fig. 5a. Fig. S18 Magnified chromoamperometry curves of Co-B-P/NF at overpotentials of 88 mv (a) and 165 mv (b). Fig. S19 Polarization curves of Co-B-P/NF (a) and Pt/C (b) in 1 M KOH before and after 1000 cycles at a scan rate of 100 mv s 1. 9

Fig. S0 (a) The SEM image and (b) EDS spectrum and elemental composition (inset) of Co-B-P/NF after the HER measurement at an overpotential of 88 mv for 0 h. The loading of Co-B-P on the Ni foam substrate before (5.1 mg cm - ) and after (4.96 mg cm - ) HER durability test was nearly maintained, indicating the good mechanical stability of the in-situ grown Co-B-P catalysts even at large working current density. Fig. S1 High-resolution XPS spectra of (a) Co P, (b) B 1s and (c) P p after the HER measurement at an overpotential of 88 mv for 0 h. Fig. S The SEM images of Pt/C (0 wt%) loaded on Ni foam before (a,b) and after (c,d) the HER measurement. 10

Table S1. Comparison of the electrocatalytic HER activity of representative nonprecious HER catalysts in 1.0 M KOH electrolyte. Overpotential (mv) at Catalyst Tafel slope (mv dec 1 ) Ref. 10 ma cm Co-B-P/NF 4.1 4 This work. MoC@NC 60 S FeB 87.5 61 S3 Ni-Co-P Nanocubes 60.1 150 S4 Co-NRCNTs 370 S5 Co9S8/CC 83 150 S6 EG/H-Co0.85Se P 13. 150 S7 NiCoP/rGO 14.1 09 S8 CoP/RGO 96 330 S9 Co/Co3O4 90 90 S10 Co3O4-MTA 98 S11 Co-B@CoO/Ti 78 10 S1 Co/CoP nanocrystals 66 135 S13 MoB 59 S14 CoSe/CF 5 95 S15 Ni0.89Co0.11Se MNSN/NF 5 85 S16 NiO/Ni-CNT 51 S17 Ni-Mo/Ti 78 9 S18 Co(S0.71Se0.9) 90 1 S19 Cu@CoSx/CF 61 134 S0 MoS/Ni3S 83.1 110 S1 O-CoP-3 61.1 160 S Ni-B0.54 88 135 S3 Co@BCN 103. 183 S4 rgo/wxmo1 xs 81.3 33 S5 MoC@C 71 47 S6 11

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