Thermodynamics of cathodic ZnTe electrodeposition using basic ammoniacal electrolytes: Why CdTe can deposit while ZnTe cannot

2Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

Potentiostatic cathodic electrodeposition of ZnTe compound was attempted using ammoniacal basic electrolytes in which Zn(II) and Te(IV) species were dissolved to form Zn(NH 3) 2+4 and TeO 2-3 ions. The ZnTe electrodeposition ended unsuccessfully although CdTe can electrodeposit from similar ammoniacal solutions under a variety of conditions. The solubility of Te(IV) species and cathodic polarization behaviors indicated the absence of interionic interaction between Zn(II) and Te(IV) ions unlike the case between Cd(II) and Te(IV). A potential-pH diagram of the Zn-Te-NH 3-H 2O system constructed based on diagrams of the Zn-NH 3-H 2O and Te-H 2O systems also demonstrated several thermodynamic and/or kinetic factors that make ZnTe deposition more difficult than those of CdTe. Copyright © 2011 De Gruyter.

Cite

CITATION STYLE

APA

Murase, K., Suzuki, T., Umenaka, Y., Hirato, T., & Awakura, Y. (2011). Thermodynamics of cathodic ZnTe electrodeposition using basic ammoniacal electrolytes: Why CdTe can deposit while ZnTe cannot. High Temperature Materials and Processes, 30(4), 451–458. https://doi.org/10.1515/HTMP.2011.068

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free