1998
DOI: 10.1006/jssc.1998.7915
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Effect of the Substitution Pattern of Diaminoanthraquinone on Some Physical Properties

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Cited by 11 publications
(3 citation statements)
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“…The signal peaks at 399.11, 400.26, and 400.97 eV in the N 1s highresolution spectrum of Figure 3e respectively represent pyridinic-N, pyrrolic-N, and graphitic-N, 38 indicating the successful doping of N introduced by the aminoanthraquinone into the CNTs. The O 1s spectrum in Figure 3f contains two peaks about 532 and 534 eV, which correspond to the C�O and C−O/C−O−C bonds, respectively, 39 not only representing the successful doping of O into the CNTs but also suggesting the successful polymerization of aminoanthraquinone on the CNTs. Therefore, modified CNTs have excellent dispersion and provide the growth of SnS with many active sites, resulting in excellent specific capacity of SDC as the anode for LIBs.…”
Section: Resultsmentioning
confidence: 99%
“…The signal peaks at 399.11, 400.26, and 400.97 eV in the N 1s highresolution spectrum of Figure 3e respectively represent pyridinic-N, pyrrolic-N, and graphitic-N, 38 indicating the successful doping of N introduced by the aminoanthraquinone into the CNTs. The O 1s spectrum in Figure 3f contains two peaks about 532 and 534 eV, which correspond to the C�O and C−O/C−O−C bonds, respectively, 39 not only representing the successful doping of O into the CNTs but also suggesting the successful polymerization of aminoanthraquinone on the CNTs. Therefore, modified CNTs have excellent dispersion and provide the growth of SnS with many active sites, resulting in excellent specific capacity of SDC as the anode for LIBs.…”
Section: Resultsmentioning
confidence: 99%
“…Therefore the band gap can be estimated from the electrochemical measurements, here it is 1.76 eV. The value obtained can be compared to the one measured by optical method, 1.8 eV, which allows to check the electrochemical measurement 137 .…”
Section: Electrochemicalmentioning
confidence: 99%
“…[5][6][7] Different functional derivatives of 9,10-anthraquinone have been synthesized and studied by various researchers. [8][9][10][11][12][13] Moreover, the electronic properties of 9,10-anthraquinones are strongly affected by the nature and position(s) of their substituent(s). The increase in electron-donating ability(ies) of the substituent(s) at various positions of 9,10-anthraquinones markedly affects the colour and redox properties of the molecules.…”
Section: Introductionmentioning
confidence: 99%