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Mechanistic Insight on the Formation of GaN:ZnO Solid Solution from Zn-Ga Layered Double Hydroxide Using Urea as the Nitriding Agent
Author(s) -
Kiyofumi Katagiri,
Yuki Hayashi,
Risa Yoshiyuki,
Kei Inumaru,
Tomoki Uchiyama,
Noriyuki Nagata,
Yoshiharu Uchimoto,
Akinobu Miyoshi,
Kazuhiko Maeda
Publication year - 2018
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/acs.inorgchem.8b02498
Subject(s) - chemistry , nitriding , hydroxide , urea , chemical engineering , inorganic chemistry , nitrogen , organic chemistry , engineering
A solid solution of GaN and ZnO (GaN:ZnO) is promising as a photocatalyst for visible-light-driven overall water splitting to produce H 2 . However, several obstacles still exist in the conventional preparation procedure of GaN:ZnO. For example, the atomic distributions of Zn and Ga are nonuniform in GaN:ZnO when a mixture of the metal oxides, i.e. Ga 2 O 3 and ZnO, is used as a precursor. In addition, GaN:ZnO is generally prepared under a harmful NH 3 flow for long durations at high temperatures. Here, a facile synthesis of GaN:ZnO with homogeneous atomic composition via a simple and safe procedure is reported. A layered double hydroxide (LDH) containing Zn 2+ and Ga 3+ was used to increase the uniformity of the atomic distributions of Zn and Ga in GaN:ZnO. We employed urea as a nitriding agent instead of gaseous NH 3 o increase the safety of the reaction. Through the optimization of reaction conditions such as heat treatment temperature and content of urea, single-phase GaN:ZnO was successfully obtained. In addition, the nitridation mechanism using urea was investigated in detail. NH 3 released from the thermal decomposition of urea did not directly nitride the LDH precursor. X-ray absorption and infrared  spectroscopies revealed that Zn(CN 2 )-like intermediate species were generated at the middle temperature range and Ga-N bonds formed at high temperature along with dissociation of CO and CO 2 .

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