Electronic Supplementary Material

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Electronic Supplementary Material
Fluorometric determination of cadmium (II) and mercury (II) using nanoclusters
consisting of a gold-nickel alloy
Zhong-Xia Wang, Yun-Xia Guo and Shou-Nian Ding*
Jiangsu Province Hi-Tech Key Laboratory for Bio-medical Research, School of Chemistry
and Chemical Engineering, Southeast University, Nanjing 211189, China
*Corresponding author, (S.-N. Ding) Fax: (+86) 25-52090621. E-mail: snding@seu.edu.cn
Figure S1 Photographs of BSA-Au-Pt NCs (a, 400 μg mL−1) and BSA-Au-Ni NCs (d, 400 μg
mL−1) in the presence of concentrations of Cd2+ ions (b, e, 50 µM) and Hg2+ ions (c, f, 20 µM),
respectively .
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Figure S2 TEM of the BSA-Au-Ni NCs. Inset: the diameter distribution of BSA-Au-Ni NCs.
Figure S3 Fluorescence spectra of the BSA (a), BSA-Ni NCs (b), BSA-Au NCs (c) and
BSA-Au-Ni NCs (d) at excitation wavelengths 340 nm, both the excitation and emission slit
widths were 5 nm.
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Figure S4 Photostability of the BSA-Au-Ni NCs as a function of the storage time, both the
excitation and emission slit widths were 5 nm.
Figure S5 The fluorescence intensity ratios (FL640nm/FL405nm) of BSA-Au-Ni NCs at 640 nm to
that at 405 nm (excitation at 340 nm) at various pH values.
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Figure S6 The fluorescence intensity ratios (FL640nm/FL405nm) of BSA-Au-Ni NCs at 640 nm
to that at 405 nm (excitation at 340 nm) in the different concentration of NaCl solution.
Figure S7 Fluorescence spectra of the BSA (a), BSA-Au-Ni NCs (b), and BSA-Cd(II)
complex (c) at excitation wavelengths 340 nm, both the excitation and emission slit widths
were 5 nm. The BSA concentration is 400.0 µg mL-1, and the concentration of Cd(II) in
BSA-Cd(II) complex is 200 µM.
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Table S1. Comparison of the linear range and detect limit for Cd2+ or Hg2+ ions different
fluorescent probes
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