Furthering the reaction mechanism of cationic vanadium clusters towards oxygen

Zhang, H; Wu, H; Geng, L; Jia, Y; Yang, M; Luo, Z

HERO ID

6308205

Reference Type

Journal Article

Year

2019

Language

English

PMID

31099360

HERO ID 6308205
In Press No
Year 2019
Title Furthering the reaction mechanism of cationic vanadium clusters towards oxygen
Authors Zhang, H; Wu, H; Geng, L; Jia, Y; Yang, M; Luo, Z
Journal Physical Chemistry Chemical Physics
Volume 21
Issue 21
Page Numbers 11234-11241
Abstract Vanadium is a polyvalent metallic element. The fact that V-O bears a much larger bond energy than the V-V metal bond challenges the preparation of pure vanadium clusters and the observation of their reactions with oxygen-containing chemicals. Utilizing a customized reflection time-of-flight mass spectrometer (Re-TOFMS), here we have prepared well-resolved small and large cationic vanadium clusters Vn+ (n < 30), and we conducted a comprehensive study on their reactivity with oxygen. It is illustrated that cationic Vn+ clusters readily react with oxygen leading to the production of both etched building blocks and oxygen-rich VnOm+ (n < m) species profiting from the ion-molecule attraction and hence increased collisional cross section. Furthermore, DFT-based energy calculations reveal that the oxygen-addition reactions are thermodynamically and kinetically favorable pathways. Also the generalized charge decomposition analysis (GCDA) illustrates that the ion-molecule charge-transfer interactions initiate the incorporation of vanadium oxides. This finding of synchronous channels of both etching and growth of vanadium clusters clarifies the reactivity of Vn+ clusters with oxygen, interprets the readily formed VnOm+ clusters within the classification of the CxAyBz series (A = VO2, B = VO3, C = VO), and enriches the understanding of the industrial chemistry of vanadium.
Doi 10.1039/c9cp01192g
Pmid 31099360
Wosid WOS:000471025900037
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English