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EPNM-2012 Shock Physics & Chemistry Research Group, BIT http: //shock.bit.edu.cn/
Elemental doping and phase transition of TiO2 induced by
shock wavesPengwan CHEN, Xiang GAO, Naifu CUI,
Jianjun LIU*
Beijing Institute of Technology *Beijing University of Chemical Technology
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EPNM-2012 Shock Physics & Chemistry Research Group, BIT http: //shock.bit.edu.cn/
Beijing Institute of Technology (BIT) was founded in 1940;
3,500 teachers and research staff;
51,000 students, including 8,200 master students , 2,500 Ph.D
students;
5 campuses, 18 schools.
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BIT Main Campus LiangXiang Campus
Zhuhai Campus West Mountain Campus
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EPNM-2012 Shock Physics & Chemistry Research Group, BIT http: //shock.bit.edu.cn/
State Key Laboratory of Explosion Science and Technology (SKLEST)
Research areas:Theory and Applied Technology of Energetic Materials;Detonation and Explosion Technology;Impact Dynamics of Materials;Explosion Effects and Protection Technology;Explosion Safety and Assessment.
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Facilities
Φ 57mm gas gun Φ 37mm gas gun
two-stage gas gun three-stage gas gun (under construction)
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Facilities
Electric gun Shock wave tube
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Facilities
Explosion chamber and Flash x-ray High speed camera
VISAR
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Explosion chamber
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Detonation-synthesized diamond
Shock-synthesized diamond
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Explosive welding
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Explosive hardeningExplosive powder compaction
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• More than 10 plants dealing with explosive cladding;
• Output value of explosive clad metals is ¥6-7 billion ($1 billion) in 2011;
• About 15 research institutes engaged in explosive production of new materials;
• National conference on explosive synthesis of materials is held every year.
Explosive welding in China
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International Explosives, Propellant and Pyrotechnic Symposium
International Safety Science and Technology Symposium International Workshop on Intensive Loading and Its Effects
International conferences organized
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Academic exchange
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Outline
2
3
4
Shock induced doping of TiO2
Shock synthesis of high pressure phase of TiO2
Photoresponse properties of shock treated TiO2
1 Introduction
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Elemental doping of TiO2
TiO2 semiconductor has oxidative capacity, chemical stability and low cost advantages.
Main drawback: energy gap is rather large, thus TiO2 is only active in the ultraviolet region (λ<420 nm) accounting for less than 5% of the natural solar light.
Element-doped TiO2 will enhance visible-light absorption and reduce energy gap.
Conventional doping methods: Sputtering; Ion implantation; Chemical vapor deposition; Hydrolysis.
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Elemental doping of TiO2
TiO2(anatase)
Eg=3.2eV;
ex387nm
Et 3%
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Phase transition of TiO2
Three common phases of TiO2 in nature
Anatase (Eg=3.2 eV)
rutile (Eg=3.2 eV)
brookite (Eg=3.4 eV) High-pressure phases (Srilankite, columbite, baddeleyite,
fluorite) may exhibit different electronic and optical. Srilankite TiO2 has been observed by shock induced phase
transition, but pure phase has not been obtained.
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Materials Precursors for doping: P25 TiO2 (15-20 nm) H2TiO3 Nitrogen doping resources : dicyandiamide (DCD, C2N4H4) hexamethylene tetramine (HMT, C6N4H12) sodium amide (NaNH2) ammonium nitrate(NH4NO3) Precursor for high-pressure phase synthesis: MC-150 TiO2 ( 5 nm) T2 TiO2 ( 100 nm)
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Content
2
3
4
Shock induced doping of TiO2
Shock synthesis of high pressure phase of TiO2
Photoresponse properties of shock treated TiO2
1 Introduction
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sample
P25 TiO2 +10wt% C2N4H4
P25 TiO2 +10wt% C2N4H4
P25 TiO2
P25 TiO2 +10wt% C2N4H4
P25 TiO2 +10wt% C2N4H4
700
FlyerVelocity(km/s)
-
1.20
1.90
2.25
ShockPressure(Gpa)
-
6.3
11.9
15.8
18.3
Shock Temperature (K)
CutoffwaveLength(nm)
2000
1800
1300
400
N-dopedConcentration(at%)
Band-gapWidth(ev)
AnatasePhaseContent(%)
RutilePhaseContent(%)
SrilankitePhaseContent(%)
-
2.52
435
698
710
730
3.10
2.85
1.78
1.75
1.70
-
3.67
9.22
11.28
13.45
50.7
67.7
81.9
85.3
46.9
14.7
18.1
21.0
27.5
30.1 23.0
21.8
11.3
0
0
P25 TiO2 +10wt% C2N4H4 3.37 29.4 2700 765 1.62 13.58 21.1 24.9 54.0
Effects of shock wave intensity
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XRD analysis
10 20 30 40 50 60 70 80 90
f
C2N4H4
e
d
c
b
a
Inte
nsity
/(a.u
.)
2/(O)
srilankiterutileanatase
Srilankite content (%)
54
23
21.8
11.3
0
RAAAAA AAKAKW /
RAARR AAKAW /
XXRAAXXX AKAAKAKW /
XRD patterns of shock-recovered samples at different conditionsUnshocked P25 TiO2 (a),
shock-recovered C serial sample(P25+C2N4H4(10%)) at 1.20km/s (b), 1.90km/s (c), 2.25km/s (d), 2.52km/s (e) and 3.37km/s (f)
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200 300 400 500 600 700 800
f
edc
b
a
Abs
orba
nce
Wavelength/(nm)
Phase change
Nitrogen dopingShock induced Activation
1240gE
UV-vis Spectra of Recovered sample P25 TiO2 raw material (a); shocked P25 TiO2 (b);
shock-recovered A, B, C serial samples at 2.25km/s (c, d, e)A: P25+C2N4H4 (1%), B: P25+C2N4H4 (5%), C: P25+C2N4H4 (10%)
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Content
2
3
4
Shock induced doping of TiO2
Shock synthesis of high pressure phase of TiO2
Photoresponse properties of shock treated TiO2
1 Introduction
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Experimental conditions and results of shock induced phase transition
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XRD analysis
10 20 30 40 50 60 70 80 90
ed
c
b
Inte
nsity
/(a.u
.)
2/(O)
srilankite rutileanatase
a
Unshocked MC-150 TiO2 (a), shocked MC-150 TiO2 at 2.56 km/s (b)shocked MC-150(10%)+Cu at 2.73 km/s (c), 3.07 km/s (d), 3.37 km/s (c)
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Synthesis of high-pressure phase of TiO2( T2)
XRD patterns of shock-recovered samples shocked Cu+ T2(20 %),a-b,at 3.37km/s
10 20 30 40 50 60 70 80 90
inte
nsity
a.u.
()
2
srilankite anatase
a
b
c
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100 200 300 400 500 600 700 800 900 1000
Wavelength/nm
a
b
a-400
b-403
200 300 400 500 600 700 8000.0
0.1
0.2
0.3
0.4
0.5
Abso
rban
ce
Wavelength/(nm)
a
b
a-400
b-403
UV-vis Spectra of Srilankite TiO2 Raman Spectra of Srilankite TiO2
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Thermal stability
10 20 30 40 50 60 70 80 90
0
2000
4000
6000
8000
10000
inte
nsity
/(a.u
.)
2
abcdefghi
-10
-8
-6
-4
-2
0
2
Hea
t Flo
w (W
/g)
98.0
98.5
99.0
99.5
100.0
100.5
Wei
ght (
%)
0 200 400 600 800 1000 1200
Temperature (°C)
Sample: 400aSize: 7.1050 mg DSC-TGA
File: D:\专业\TG-DSC\403a.001
Run Date: 22-Feb-2012 16:19Instrument: SDT Q600 V20.9 Build 20
Exo Up Universal V4.7A TA Instruments
TG-DSCXRD at elevated temperatures
300 (a),400 (b),500 (c),600 (d),700℃ ℃ ℃ ℃ ℃(e),800 (f),900 (g),1000 (h),1100 (i)℃ ℃ ℃ ℃
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Content
2
3
4
Shock induced doping of TiO2
Shock synthesis of high pressure phase of TiO2
Photoresponse properties of shock treated TiO2
1 Introduction
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Photocatalytic evaluation of N-doped TiO2 and high pressure phase TiO2
1 4
26
5
3
Schematic of photocatalytic degradation
1. Xenon lamp; 2. Rubber stopper; 3. Reactor; 4.Water and photocatalyst; 5. Stirrer; 6. dark box
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0 10 20 30 40 50
a b c d e f g h
Degradation to RB of 10 ppm under visible light irradiationwith a filter of 400 nm
Abs
orba
nce
Reaction time/(min)
Photocatalytic degradation of rhodamine B using N-doped TiO2(Moderate shock intensity is preferred)
P25 TiO2+10wt%C2N4H4 1.2 km/s(a), 2.52 km/s(b), 2.25 km/s(c), 1.90 km/s(d ), 1.79 km/s(h);(e) P25 TiO2+5wt%C2N4H4 2.25 km/s;
(f) P25 TiO2+1wt%C2N4H4 2.25 km/s; (g) P25 TiO2 2.25 km/s
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Photocatalytic degradation ofdifferent samples to methylene blue (MB)(a)P25+C2N4H4(10%) at 2.25km/s;(b)H2TiO3+ C2N4H4(10%) at 2.74km/s;(c)H2TiO3+ C2N4H4(10%) at 2.25km/s.
Photocatalytic degradation ofdifferent samples to Rhodmine B (RB)(a)P25+C2N4H4(10%) at 2.25km/s;(b)H2TiO3+ C2N4H4(10%) at 2.25km/s;(c)H2TiO3+ C2N4H4(10%) at 2.74km/s.
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0 10 20 30 40 50 60 70
Abs
orba
nce
Reaction time / (min)
b
a
Photocatalytic Degradation of Methylene blue using high-pressure phase TiO2
(a) MC-150TiO2+90wt%Cu 3.07 km/s; (b) MC-150 TiO2+90wt%Cu 3.37 km/s
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Photo electrochemical activity of TiO2 after shock processing
I-V
Powder sample and Graphene
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Photo electrochemical activity of N-doped TiO2
0.008 10-4A
5times0.04 10-4A
10times
0.08 10-4A
Photo electrochemical activity of N-doped TiO2 under visible light irradiation(a) Raw TiO2; (b) shock treatment at 1.2km/s; (c) shock treatment at 2.25km/s
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Photo electrochemical activity of high-pressure phase of TiO2
Good stability
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sample
a/b/c
Flyervelocity(km/s)
1.20
Cutoffwavelength(nm)
450
N-dopedconcentration(at%)
Band-gapwidth(ev)
Anatasephasecontent(%)
Rutilephasecontent(%)
Srilankitephasecontent(%)
2.76 0.76 71.4 11.8 16.8
0 100 200 300 400 500 600 700 8000.0
0.5
1.0
1.5
2.0
2.5
Curr
ent
dens
ity(
mA)
vol tage(mV)
a
0 100 200 300 400 500 600 700 8000
1
2
3
4
5
Curr
ent d
ensi
ty (m
A)
Voltage (mV)
b
0 100 200 300 400 500 600 700 8000
1
2
3
4
5
6
7
8
Cur
rent
den
sity
(mA
)
Voltage(mV)
c
Sample
a
b
c
Sample preparation Isc(mA/cm2) Voc(mV) ff(%) n(%)
Smear two layer and sinter
Smear one layer and sinterSmear one layer and sinter
Smear one layer and sinterSmear two layer and sinter
5.00
3.20 0.71
753
725
738
7.30
1.66
2.66
4.170.75
0.76
DSSC performance of shock induced N-doped TiO2
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• Nitrogen doped TiO2 was obtained by shock treatment of a mixture of TiO2 precursor and nitrogen resources. Nitrogen doped TiO2 exhibits enhanced visible-light photocatalytic activity.
• Pure Srilankite TiO2 can be obtained by shock-induced phase transition;
• Shock-induced doping might be a promising method for powder modification.
Conclusions
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EPNM-2012 Shock Physics & Chemistry Research Group, BIT http: //shock.bit.edu.cn/
Thank you for your attention!
http://shock.bit.edu.cn
E-mail: [email protected]