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Title: Synthetic approaches to borocarbonitrides, BC{sub x}N (x=1-2)

Journal Article · · Journal of Solid State Chemistry
; ; ; ;  [1];  [1]
  1. Chemistry and Physics of Materials Unit, CSIR Centre of Excellence in Chemistry and International Centre for Materials Science, Theoretical Sciences Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bangalore 560064 (India)

In order to synthesize borocarbonitrides of the general formula BC{sub x}N where x varies between 1 and 2, we have carried out high-temperature gas phase reaction of BBr{sub 3} with a mixture of ethylene and ammonia. The composition of the product was close to BC{sub 1.6}N as shown by x-ray photon spectroscopy (XPS) and electron energy loss spectroscopy (EELS). The products were further characterized by infra-red, Raman and other spectroscopic techniques. The borocarbonitrides obtained from the gas phase reaction have low surface areas, in contrast to those of similar compositions prepared by the urea method. First principles calculations show that the most stable structures of the compositions BCN and BC{sub 2}N contain BN-rich and carbon-rich domains where BN{sub 3} and NB{sub 3} units are present. - Graphical abstract: Vapor phase synthesis of BC{sub x}N (x=1-2) by the reaction of BBr{sub 3}, ethylene and ammonia leads to the formation of pan-like structure. Highlights: > We have carried out vapor phase reaction of BBr{sub 3}, ethylene and ammonia to synthesize BC{sub x}N (x=1-2). > HRTEM and AFM show the formation of pan-like structures with the central region formed of single layer of BC{sub x}N. > Borocarbonitrides formed by vapor phase synthesis show limited adsorption properties as compared to the urea route. > First principles calculations show that the most stable structure of the compositions BCN and BC{sub 2}N contain BN-rich and carbon-rich domains where BN{sub 3} and NB{sub 3} units are present.

OSTI ID:
21580055
Journal Information:
Journal of Solid State Chemistry, Vol. 184, Issue 11; Other Information: DOI: 10.1016/j.jssc.2011.08.034; PII: S0022-4596(11)00474-9; Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; ISSN 0022-4596
Country of Publication:
United States
Language:
English