Title: Why nano sized Pt
1Why nano sized Pt?
- Why certain cluster sizes of platinum are more
active ? - Is it due to d- orbital like conventional
catalysis? - What other factor?
How to study?
2Molecular modeling
- Understanding the fundamental
- Density Functional Theory (DFT)
- (DMol3 software)
- Stabilization energy, orbital nature and
contribution - Metal cluster (Pt) size (1-14)
3Results
Stabilization energy Total energy of
cluster-Total energy of Pt atom No. of atoms /
No. of atoms
4(a). Stabilization energy of various Pt clusters,
(b). The energy of HOMO-LUMO frontier orbital of
various Pt clusters.
5Percentage contribution of orbital at HOMO
6(No Transcript)
7How to validate the concept?
(c)
(a)
(b)
- SWNT-arm chair type (5, 5)- diameter of 6.78 Å
and length 9.8 Å - Nitrogen - substituted in the terminal carbon
of CNT (NCNT) - DFT- to optimize, reacted with single Pt atom
then formic acid
8Results
- The binding energy of Pt to NCNT (-3.26 eV) is
greater than that of pure CNT (-13.94 eV). - Interaction energy of formic acid is 0.25 eV
higher for Pt-NCNT then Pt-CNT composite
9Proposed work
- Put the various clusters of pt on the CNT and
NCNT to study the binding energy of the cluster
as the size changes. - Identify the cluster which is having higher
binding energy with the CNT and evaluate
interaction energy of the formic acid with the
cluster. - A possible reaction pathway with all transition
state theory calculation to predict the
intermediate in formic acid oxidation will be
proposed with a simple cluster model.
10Experimental results
- Formic acid electrooxidation on 3 different
carbon supports - Vulcan XC-72 (commercial standard)
- MWNTs functionalized using oxidative route
(F-MWNTs) - (refluxing MWNT with 13 ratio of H2SO4HNO3)
- Nitrogen containing carbon nanotubes (NCNT)
- (template method using alumina membranes)
- Pt was deposited electrochemically
- sweeping the potential between -0.25 to 1 V vs
Ag/AgCl for 20 cycles in chloroplatinc acid
solution
11CO stripping voltammograms over pt loaded catalyst
CO stripping experiment were carried out n 0.5 M
H2SO4
12cyclic voltammograms of formic acid oxidation
over pt loaded catalyst
Formic acid oxidation was performed in a 0.5 M
H2SO4 0.5 M HCOOH solution by cycling between
-2 to 0.95 V vs Ag/AgCl.
13Variation of current density with time
0.5 M H2SO4 / 0.5 M HCOOH at 0.6 V vs Ag/ AgCl
14Proposed work
- Optimization of platinum loading to correlate
activity of the platinum cluster size - Deposition of platinum by other methods
- To find mechanistic pathway for formic acid
oxidation