Published May 5, 2005 | Version v1
Journal article

Study of the effects of nanometer β-Ni(OH)2 in nickel hydroxide electrodes

  • 1. Chemistry Laboratory Center, Department of Chemistry, Harbin Institute of Technology, Harbin 150001 (China)
  • 2. Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100039 (China)

Description

Nanometer β-Ni(OH)2, showed by XRD, was prepared by our supersonic coordination-precipitation method, with an average grain size of about 50 nm by TEM. Proton diffusion coefficient of nanometer Ni(OH)2 and spherical Ni(OH)2 were 1.93 x 10-11, and 5.50 x 10-13 cm2/s, respectively, with combination of chronocoulometry and cyclic voltammetry. Charge-discharge test of simulated batteries at 0.2 deg. C showed that addition of 8 mass% of our prepared nanometer Ni(OH)2 in nickel hydroxide electrodes led to increases in cathode discharge specific capacity (CDSC) by nearly 10% and the chargeability of the electrode by about 50 mAh/g, and a decrease in polarization. Cycle life test of AA-type MH-Ni batteries discovered that effect of nanometer Ni(OH)2 in increasing CDSC was more apparent for the first 100 cycles and not much difference was found after 350 cycles. XAS demonstrated a higher oxidation state of Ni in fully charged nanometer Ni(OH)2 composite electrode (Nano-E) and a lower one in discharged Nano-E, compared with micrometer Ni(OH)2 spherical electrodes (Micro-E). A larger structure distortion was found in Nano-E, offering more vacancies for proton diffusion. Thus conversion between Ni2+ and Ni3+ was promoted during the charge-discharge process, which was assumed to be one explanation of increasing CDSC with the addition of nanometer Ni(OH)2

Additional details

Identifiers

DOI
10.1016/j.electacta.2004.11.025;
PII
S0013-4686(04)01141-7;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
50
Journal Issue
14
Journal Page Range
p. 2763-2769
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.