pcat.cat.hokudai.ac.jppcat.cat.hokudai.ac.jp/class/pc2020/20200813_bo_sapporo.pdf2020/08/13 ·...
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![Page 1: pcat.cat.hokudai.ac.jppcat.cat.hokudai.ac.jp/class/pc2020/20200813_BO_Sapporo.pdf2020/08/13 · Advanced Course in Environmental Catalytic Reaction Chemistry I. 2. Advanced Course](https://reader035.vdocuments.net/reader035/viewer/2022081614/5fd10933a38ef0586b6e8c39/html5/thumbnails/1.jpg)
Advanced Course in Environmental Catalytic Reaction Chemistry I 1
2020/08/13
環境触媒化学特論I
15
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Advanced Course in Environmental Catalytic Reaction Chemistry I 2
Advanced Course in Environmental Catalytic Chemistry I
understanding chemistry by understanding photocatalysisunderstanding photocatalysis by understanding chemistry
Division of Environmental Material Science, Graduate School of Environmental ScienceThe first semester of Fiscal 202008:45─10:15, Thursday on Zoom
Bunsho Ohtani
Institute for Catalysis, Hokkaido University, Sapporo 001-0021, Japan011-706-9132 (dial-in)/011-706-9133 (facsimile)
[email protected]://pcat.cat.hokudai.ac.jp/pcat
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Advanced Course in Environmental Catalytic Reaction Chemistry I 3
schedule
(1) May 7 introduction of photocatalysis(2) May 14 interaction between substances and light(3) May 21 electronic structure and photoabsorption(4) May 28 thermodynamics: electron and positive hole(5) June 4 adsorption(6) June 11 kinetic analysis of photocatalysis(7) June 18 steady-state approximation(8) June 25 kinetics and photocatalytic activity(9) July 2 action spectrum analysis (1)(10) July 9 action spectrum analysis (2)(11) July 16 light intensity-dependence analysis(12) July 23 crystal structure (1)(13) July 30 crystal structure (2)(14) August 6 design and development of photocatalysts (1)(15) August 13 design and development of photocatalysts (2)
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Advanced Course in Environmental Catalytic Reaction Chemistry I 4
format
Please send email in Japanese or English within 72 hoursto: [email protected]: pc2020MMDD-XXXXXXXX
[email protected](full name)(nickname)(what is learnt in this lecture series) + (questions if any)[blank line](answer for question 1)(answer for question 2)(answer for question 3)・・
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Advanced Course in Environmental Catalytic Reaction Chemistry I 5
email example
to
subject
(same as subject)email addressfull namenicknamecomment(s) +
question(blank line)answer 1answer 2answer 3・・
pc20200813-57388301
pc20200813-57388301
pc20200813-57388301
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Advanced Course in Environmental Catalytic Reaction Chemistry I 6
special report (20 + α points)
special report for extra (bonus) score (20 point)report on critical review on "photocatalysis" in Wikipedia, pointing out errors, misunderstanding and speculationsbased on the contents of this lecture.http://en.wikipedia.org/wiki/Photocatalysishttp://ja.wikipedia.org/wiki/光触媒
• Japanese or English• A4 size 2 pages• submission by email attachment• a PDF file is more preferable than a Word file• email title: pc20200820-XXXXXXXX• file name: pc20200820-XXXXXXXX.pdf (or .docx or .doc)• deadline of submission: August 20, 2020 23:59
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Fujishima, A.; Honda, K., Nature 238, 37 (1972).
19,910 citationsat July 3, 2020
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8B. Ohtani, "Photocatalysis A--Z: What We Know and What We Don't Know", J. Photochem. Photobiol. C: Photochem. Rev., 11 (2010) 157-178.
band-structure model (BSM)
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band structure (for an infinite-sized crystal)
CB
VB
surfacesurface
band-structure modelbulk only = no surface/size properties
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homogeneous and heterogeneous photocatalysis
e
e
molecule/metal complex particle
LUMO
HOMO
CB bottom
VB toph
e
2H2O
O2 + 4H+
+1.23 V
4h+
band-structure modelno multielectron-transfer concept
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ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
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ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
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RDB-PAS reversed double-beam photoacoustic spectroscopy
enables measurements of
ERDT/CBB patternsenergy-resolved distribution of electron traps/conduction-band bottom
of semiconductor (metal oxide) solids for
• identification (as a novel concept)
• detailed characterization
electron trap
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macro- micro-scopic scopic
surface
bulk
XRD
TEM
STM AFM
SSA(specific surface area)
XPS
UPS
EDX
Raman
IRED
(electron diffraction)solid NMR
LEED
XRF
RDB-PAS
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minimum requisits for
identification bulk structure bulk/surface size surface structure
ener
gy fr
om v
alen
ce-b
and
(VB)
top/
eV
3.4
3.2
3.0
2.8
2.6
2.4
2.2
2.0
20100
<97>
CB
ET density/µmol g-130
CBBbulk structure
conduction-band bottom
TDbulk (surface) size
total ET density
energy-resolveddensity of ETs
ERDTsurface structure
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ERDT: energy-resolved distribution of traps
ET density/μmol g-1
anatase anatase rutile rutileonly > rutile > anatase only
ET density/μmol g-1 ET density/μmol g-1ET density/μmol g-1
fingerprint of titaniaslike NMR patterns for organic molecules
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replotting of data withseven-point non-weightedmoving average
● CH3OH → HCHO + H2● CH3COOH + 2O2 → 2CO2 + 2H2O● 4Ag+ + 2H2O → 4Ag + O2 + 4H+
degree of coincidence
0
0.2
0.4
0.6
0.8
1
0 0.2 0.4 0.6 0.8 1
ζ pc
ζ
0
0.2
0.4
0.6
0.8
1
0 0.2 0.4 0.6 0.8 1
ζpc
ζ
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identification of
powders (semiconducting materials with band gap and ETs)
bulk composition CBB bulk size (surface size) total ET density surface structure ERDT pattern
XRD patternnitrogen ads. (BET)-----
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物質の同定
identificationpurity
純度
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octahedral anatase particles (OAP)• naturally occurring (but
contaminated)• 8 equivalent {101} facets• possible morphology dependent
photocatalytic activity
(101)
O
Ti
Amano, F.; Yasumoto, T.; Prieto-Mahaney, O.-O.; Uchida, S.; Shibayama, T.; Ohtani, B. Chem. Commun. 2009, 2311-2313.
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bulk (crystal) surfacesize
homogeneoussize distribution
pure!
100% crystalline(anatase)
pure!
100% {101}(octahedral)
pure!
純物質/標準物質
pure/authentic sample
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%anatase 94 97 99 99
%OAP 76 96 92 96
ssa/m2 g-1 31 21 17 15
dET/μmol g-1 31 21 18 18
size/nm 121 183 228 291
Yumin LI
hydrothermally synthesizedoctahedral anatase (A) particles (OAPs)
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0%
20%
40%
60%
80%
100%Pe
rcen
tage
of
num
ber o
f par
ticle
s w
ithin
a ra
nge
±5%
±10%
±15%±20% ±30%
ca. 80% in ±20% size
%anatase 94 97 99 99
%OAP 76 96 92 96
ssa/m2 g-1 31 21 17 15
dET/μmol g-1 31 21 18 18
size/nm 121 183 228 291
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total ET density and specific surface area
y=0.87x+3.56R2=0.958
0 5 10 15 20 25 30 350
5
10
15
20
25
30
35To
tal d
ensi
ty o
f ETs
/ μm
ol g
-1
Specific surface area / m2g-1specific surface area/m2 g-1
tota
l ET
dens
ity/μ
mol
g-1
slope (0.87) =
ca. 0.5 ETs/nm2ca. 0.5 ET nm‒2
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ERDT-pattern purity
normalized at peak tops
similar narrower width for OAPs
wider width for commercial sample
single Gaussian fits
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5-coordinated Ti6-coordinated Ti4-coordinated Ti
Shirai, K.; Fagio, G.; Sugimoto, T.; Selli, D.; Farraro, L.; Watanabe, K.; Haruta, M.; Ohtani, B.; Kurata, H.; Di Valentin, C.; Matsumoto, Y. J. Am. Chem. Soc. 2018, 140, 1415-1422.
certain site ofca. 0.5 nm‒2
density
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bulk (crystal) surfacesize
homogeneoussize distribution
pure!
100% crystalline(anatase)
pure!
100% {101}(octahedral)
pure!freedom = variable
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0 50 100 150 200 250 3000
100
200
300
400R
elat
ive
activ
ities
(FP6
) (%
)
Average length of OAP / nm
O2 (Ag+)CO2
H2
average height of OAP/nm
rela
tive
activ
ity to
FP6
(%)
CH3COOH + 2O2
→ 2CO2 + 2H2O
CH3OH → HCHO + H2
4Ag+ + 2H2O → 4Ag + O2 + 4H+
particle size-dependent activitytrue
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ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
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♪
modulated light continuous light
methanol saturatedargon gas atmosphere
625 nm80 Hz
scanning
CB
VB
direct excitation
filling electron traps selectively from deeper side
reversed double-beam photoacoustic spectroscopy (RDB-PAS)
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ca. 0.1-0.2 eV shiftenergy difference between VBT and high DOS part
RDB-PAS
photochemical method
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absorption-edge wavelength• absorption edge: corresponding to band gap• apparently the edge is not SHARP due to distribution of "density of
states"
DOSdensity of states
negligible DOS at the edges = less photoabsorption
h-DOS
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brookite
BCB
20100
<69>NTB-1
brookite
0 10 20 30
<192>Wakoamor-phous
CB
anatase
A A +R R +A
rutile
R
amorphouscommercial titania powders
ET density/µmol g-1
ener
gy fr
om V
B to
p/eV
ener
gy fr
om h
-DO
S(VB
)/eV
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ERDT patterns of anatase-rutile mixture
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orbital overlapping
h-DOS
h-DOS
ET of anatase
VB of rutileh-DOS
energy difference in VB-ET excitation
ET of rutile
VB of anatase
ICTEinterfacial charge-transfer excitation through spaciallyoverlapped orbitals of contacted particles
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ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
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so-called "band-structure" model of photocatalysis
CB
VBh
e
h+
e-
size?
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2H2O O24e-
-4e-
photocatalytic solar hydrogen production/carbon dioxide fixation
photocatalytic organics decomposition
thermodynamically favorable: ΔG < 0
thermodynamically unfavorable: ΔG > 0
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water-oxygen reactions in heterogeneous photocatalysis
oxygen reduction
CB
VBh
e
O2-
O2
-0.28 V
e-
water oxidation
CB
VBh
e
2H2O
O2 + 4H+
+1.23 V
4h+
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Dr. Shugo TAKEUCHI Photocatalysis 1 Young Poster Award, First International Symposium on Recent Progress of Energy and Environmental Photocatalysis held in Tokyo University of Science (2015/09/03-04)
Faraday Division Poster Award, Faraday Discussion: Artificial Photosynthesis, Kyoto (2017/02/28-03/03)
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0
2000
4000
6000
-0.5
-0.4
5-0
.4-0
.35
-0.3
-0.2
5-0
.2-0
.15
-0.1
-0.0
50.
05 0.1
0.15 0.
20.
25 0.3
0.35 0.
40.
45 0.5
distance from the center/cm
inte
nsity
/mW
cm
-2
effective irradiationarea: 0.12 cm2
0
500
1000
1500-0
.5-0
.45
-0.4
-0.3
5-0
.3-0
.25
-0.2
-0.1
5-0
.1-0
.05
0.05 0.
10.
15 0.2
0.25 0.
30.
35 0.4
0.45 0.
5
distance from the center/cm
inte
nsity
/mW
cm
-2
effective irradiationarea: 0.64 cm2
calibrated light intensity (IL)= 0.95×312 mW/0.12 cm2 = 2470 mW cm-2
calibrated light intensity (IL)= 0.95×330 mW/0.64 cm2 = 490 mW cm-2
highly intense UV-LEDs
◯ HMP-type (unfocused)
● NSL-type (focused)
IMAX: ~340 mW/cm2
IMAX: ~500 mW/cm2
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anatase 4 nm IO3-NSL/HMP UV-LED
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TiO2
TiO2(h+)
h+ e- IO3-/Fe3+
1/τ1
ILψφIL ψ2 φ
TiO2(2h+)
h+h+
k
H2O2
O2
1/τ2
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TiO2
TiO2(h+)
h+ e- IO3-/Fe3+
1/τ1
I LψφI Lψ2φ
TiO2(2h+)
h+h+
k
H2O2
O2
1/τ2
r = I L2ψψ2φ2 / ( (1/τ1) + I L ψ2φ )
at low I L
at high I L
r = IL2ψψ2φ2τ1
r = ILψφ
I thr = 1 /ψ2φτ1
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small (×1) large (×2)ψ (S) = ψ (L)
positive hole created by first-step photon
ψ2 (S) << ψ2(L)
positive hole created by second-step photon
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TiO2
TiO2(h+)
h+ e- IO3-/Fe3+
1/τ1
I LψφI Lψ2φ
TiO2(2h+)
h+h+
k
H2O2
O2
1/τ2
I thr = 1 /ψ2φτ1
τ1
ψ2
φ
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n = 1
n = 2 (slope)ψφ1/ ψ2φτ1 = Ithr
light intensity
reac
tion
rate
two-photon absorption
guaranteed
h+h+
h+
h+h+h+h+
r = I L2ψψ2φ2 / ( (1/τ1) + I L ψ2φ )
at low I L
at high I L
r = I L2ψψ2φ2τ1
r = I Lψφ
I thr = 1 /ψ2φτ1
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O2 + e- = O2- 1 -0.56 V
O2 + e- + H+= HO2 1 -0.13 V
O2 + 2e- + 2H+= H2O2 2 0.68 V
O2 + 4e- + 4H+= 2H2O 4 1.23 V
HO2 + e- + H+ = H2O2 1 1.5 V
H2O2 + 2e- + 2H+= 2H2O 2 1.77 V
HO・+ e- + H+ = H2O 1 2.8 V
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anatase 4 nm IO3-NSL/HMP UV-LED
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IO3-
small anatase (4 nm) large anatase (170 nm)
small rutile (13 nm) large rutile (360 nm)
NSL/HMP UV-LED
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small anatase (4 nm) large anatase (170 nm)
small rutile (13 nm) large rutile (360 nm)
IO3-NSL/HMP UV-LED
LID: light intensity dependence
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O2 + e- = O2- 1 -0.56 V
O2 + e- + H+= HO2 1 -0.13 V
O2 + 2e- + 2H+= H2O2 2 0.68 V
O2 + 4e- + 4H+= 2H2O 4 1.23 V
HO2 + e- + H+ = H2O2 1 1.5 V
H2O2 + 2e- + 2H+= 2H2O 2 1.77 V
HO・+ e- + H+ = H2O 1 2.8 V
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r = I 2ψ2ψφ2 / ( (1/τ) + I ψ2φ )
at low I
at high I
r = I 2ψ2ψφ2τr = I φψ
I thr = 1 /φψ2τ
effect of oxygen-evolutionco-catalysts
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-4 -3 -2 -1 0 1 2
ln(IL/W cm-2)
3
2
1
-2
0
-1
ln(r/
μmol
h-1
cm-2
)
1
2
Bare MT150AMnO2-mix0.1 wt%MnO20.5 wt% MnO2
Bare MT150AMnO2-mix0.1 wt% MnO20.5 wt% MnO2
r = I2ψ2ψφ2 / ( (1/τ) + I ψ2φ )
at low I
at high I
r = I2ψ2ψφ2τ
r = I φψ
I thr = 1 /φψ2τ
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-5 -3 -2 -1 0 1 2
ln(IL/W cm-2)
4
2
-2
0ln(r/
μmol
h-1
cm-2
)
1
2
Bare
MnO2
CoPi
IrO2
-4
0.1 wt% loading
r = I2ψ2ψφ2 / ( (1/τ) + I ψ2φ )
at low I
at high I
r = I2ψ2ψφ2τ
r = I φψ
I thr = 1 /φψ2τ
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-4 -3 -2 -1 0 1 2
ln(IL/W cm-2)
5
2
-2
0
ln(r/
μmol
h-1
cm-2
)
1
2Bare
MnO2
IrO2
-1
1
3
4
14
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large rutile
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h+
h+
h+
EV
h+
h+h+
h+
EV
EV EV
EV EVEV
EV
EV
h+
h+
EV
EV
h+
h+
h+
h+h+
h+
EVEVEV
EVEV
loading0
loading1
loading5
volume×8
volume×8
EV governs ψ2
effective volume (EV)
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Professor Mai TAKASE
(Graduate School of Engineering, Muroran
Institute of
Ms. Haruna HORI(Ph. D.
Candidate, Graduate School of Environmental
Science, Hokkaido
Awarded "The 12th Honda-Fujishima
Prize" (March 2016)
Awarded "The Best Presentation
Award" in 2015 Summer Meeting
of Chemical Society (July
2015)
Professor Mai TAKASHIMA
(Institute for Catalysis, Hokkaido
Ms. Chiharu YAMADA
(Master course, Graduate School of
Environmental Science, Hokkaido
Awarded "The Best Presentation Award"
in 2019 Winter Meeting of
Chemistgry-related Societies (January
2019)
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BWO: bismuth tungstate (Bi2WO6) photocatalyst
433 K
403 K
463 K
photoirradiation (> 400 nm)
493 K
CO2
CO
2ev
olut
ion/
μmol
60
50
40
30
20
10
00 2 4 6 8 10
12time /h
CH3CHO + 5/2 O2 → 2CO2 + 2H2O
F. Amano, K. Nogami, B. Ohtani,Langmuir 2010, 26, 7174.
1 μm
300 nm
F. Amano, K. Nogami, R. Abe and B.Ohtani, Chem. Lett. 2007, 36, 1314.
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intensity dependence
Merck (anatase) titania
dehydrogenation of methanol<platinum-loaded/under argon>
first-order = linear
mineralization of acetic acid<under air>
0.5th = square root
at higher intensity
0th = constant rate, due to diffusion (of O2?)-limited process
light intensity/mW cm-2
appa
rent
qua
ntum
effi
cien
cy (Φ
app)
1
0.1
0.01
1
0.1
0.01
0.1 101
CH3COOH + 2O2
→ 2CO2 + 2H2O
CH3OH → HCHO + H2
290 nm
350 nm
380 nm
395 nm
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radical chain mechanism
peroxy radical as a chain carrierI : incident photon flux; f : photoabsorption efficiency; j : intrinsic quantum efficiency
stationary (steady) state approximation for RO2· and R·
RH → R·R· + O2 → RO2·RO2· + RH → RO2H + R·2RO2· → (deactivation)
I φψk1k2k3
d[R·]/dt = 0 = Iφψ - k1[R·][O2] + k2[RO2·][RH]d[RO2·]/dt = 0 = k1[R·][O2] - k2[RO2·][RH] - k3[RO2·]2
[RO2·]2 = Iφψ / k3
-d[RH]/dt = Iφψ + k2[RH][RO2·]
Φapp = φψ + k2[RH](φψ / k3)0.5I-0.5B. Ohtani, Electrochemistry, 2014, 82, 414
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square-root dependence
• Linear relations are obtained.• Y-intersect corresponding to Φ was negligible, i.e., very low intrinsic
quantum efficiency.• Appreciable photocatalytic activity might be due to long chain length.
Φap
pat
350
nm
I-0.5 / (mW cm-2)-0.5
TIO-2
Merck
0
0.2
0.4
0.6
0.8
0 0.5 1 1.5 2 2.5 3 3.5
Φapp = φψ + k2[RH](φψ / k3)0.5I -0.5
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FB
2 µm
WML
200 nm 200 nm
500FB
200 nm 200 nm2 µm
WMH
500WML 500WMH
wetmill
773 K 773 K 773 K
20m2 g-1
42m2 g-1
43m2 g-1
8m2 g-1
15m2 g-1
15m2 g-1
effective particle size
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!
activities
CH3COOH + 2O2→ 2CO2 + 2H2O
CH3OH → H2 + HCHO
4Ag+ + 2H2O→ O2 + 4Ag
CH3COOH + 2O2→ 2CO2 + 2H2O
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possible band position of BWO/tungstena
VB
CB
TiO2
number of electrons for O2 reduction
1
(BWO)
1 2 2 0
1
24
WO3-Pt WO3BWO
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2
1
0.5
WML
0.5
1
2
ln (R
/µm
ol h
-1)
FB
-5
-7
-9
-11-4 -2 0 2
ln (I /mW)86420-2
-2 0 2 4 6 8-4 864
-5
-7
-9
-11
light intensity-dependent rate by FB and WML
R = a I n → ln R = ln a + n ln I
1 µm 19.5 m2g-1
42.4 m2g-1100 nm
CH3COOH + 2O2 → 2CO2 + 2H2O
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BWO + hν → BWO(e) Iψ1Φ first excitationBWO(e) + hν → BWO(2e) Iψ2Φ[BWO(e)] second excitationBWO(2e) + RH → BWO + R・ kr [BWO(2e)][RH] radical creationR・+ O2 → RO2・ ki [R・][O2] initiationRO2・+ RH → RO2H + R・ kp [RO2][RH] propagation2RO2・→ RO4R kt [RO2・]2 terminationBWO(e) → BWO kd [BWO(e)] deactivation
model for light intensity-dependent rate
BWO: photocatalyst BWO(e): BWO with e- BWO(2e): BWO with 2e-I: light intensity Φ: quantum efficiency of e- creationψ1: absorption efficiency of PC ψ2: absorption efficiency of PC(e)kr, ki, kp, kt ,kd: rate constants
assuming initiation only by 2 e--bearing BWO (BWO(2e)) peroxy-radical chain mechanism
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2
1
0.5
WML
0.5
1
2
ln (R
/µm
ol h
-1)
FB
-5
-7
-9
-11-4 -2 0 2
ln (I /mW)86420-2
-2 0 2 4 6 8-4 864
-5
-7
-9
-11
light intensity-dependent rate by FB and WML
low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ2φ)0.5) I 0.5 Ithr = kd/(ψ2φ)
4 mW 80 mW1 µm 19.5 m2g-1
42.4 m2g-1100 nm
CH3COOH + 2O2 → 2CO2 + 2H2O
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(virtual) effective particle size = Ψ2for multielectron transfer processes
1 µm 19.5 m2g-1
42.4 m2g-1100 nm
×20
higher probability for accumulation of multiple electrons
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70
35
0
500F
BFB
WM
L
WM
H
500W
ML
500W
MH
reac
tion
rate
/µm
ol h
-1activity of BWO samples for organics decomposition
1
0.5
1 2 3 4 5 6ln (I /mW)
ln (R
/µm
ol h
-1)
2
2
500FB
FB
0.5
1
-5
-6
-7
-8
-9
low I region R = Φkp[RH] (ψ1ψ2/kdkt)0.5 I
first-order low-intensity region
CH3COOH + 2O2 → 2CO2 + 2H2O
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2
1
0.5
WML
0.5
1ln (R
/µm
ol h
-1)
FB
-5
-7
-9
-11-4 -2 0 2
ln (I /mW)86420-2
-2 0 2 4 6 8-4 864
-5
-7
-9
-11
2
light intensity-dependent rate by FB and WML
low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ2φ)0.5) I 0.5 Ithr = kd/(ψ2φ)
4 mW 80 mW1 µm 19.5 m2g-1
42.4 m2g-1100 nm
CH3COOH + 2O2 → 2CO2 + 2H2O
!
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visible light-sensitive Pt-WO3 photocatalystaction spectrum similar to diffuse reflectance spectrum
25
20
15
10
5
0550500450400350300
TiO2 P25 Pt-WO3
wavelength/nm
appa
rent
qua
ntum
effi
cien
cy/% 1.5
1.0
0.5
0.0550500450400350300
TiO2 WO3
wavelength/nm
Abs.
WO3
Pt
Pt
Abe, R.; Takami, H.; Murakami, N.; Ohtani, B., J. Am. Chem. Soc., 130, 7780–7781 (2008).
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tungstena (WO3) with/without platinum (Pt)
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VB(mainly orbital of
oxygen)
CB(mainly orbital of
titanium)
VB(mainly orbital of
sulfur)
CB(mainly orbital of
metal)
metal sulfide
band structure of metal oxides and sulfides
TiO2
metal oxide
level of one-electron oxygen
reduction
level of hydrogen production
WO3
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low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ2φ)0.5) I 0.5 Ithr = kd/(ψ2φ)
tungstena (WO3) with/without platinum (Pt)
ln (r
/μm
olh-
1cm
-2)
ln (IL /mW cm-2)
air
air
O2
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low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ2φ)0.5) I 0.5 Ithr = kd/(ψ2φ)
tungstena (WO3) with/without platinum (Pt)
ln (r
/μm
olh-
1cm
-2)
ln (IL /mW cm-2)
air
air
O2
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tungstena (WO3) with/without platinum (Pt)
rate at n = 0
diffusion of oxygen onto platinum
surface
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low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ2φ)0.5) I 0.5 Ithr = kd/(ψ2φ)
tungstena (WO3) with/without platinum (Pt)
ln (r
/μm
olh-
1cm
-2)
ln (IL /mW cm-2)
air
air
O2!
!
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82
possible band position of BWO/tungstena
VB
CB
TiO2
number of electrons for O2 reduction
1 2 0
1
24
2
WO3-Pt
Pt
WO3BWO
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ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
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85
electrochemical equilibrium = simultaneous front/backward
n-electron transfer
nnumber of electrons
ΔG =-nFEE = E0 + ln(aOX/aR) × RT / nF
digital!
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86
2
1
titania photocatalyzed oxygen evolution
singularity!
★★
★
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87
low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ1φ)0.5) I 0.5 Ithr = kd/(ψ1φ)
tungstena (WO3) with/without platinum (Pt)
ln (r
/μm
olh-
1cm
-2)
ln (IL /mW cm-2)
air
air
O2
singularity!
★★
★
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88
2
1
0.5
WML
0.5
1ln (R
/µm
ol h
-1)
FB
-5
-7
-9
-11-4 -2 0 2
ln (I /mW)86420-2
-2 0 2 4 6 8-4 864
-5
-7
-9
-11
2
light intensity-dependent rate by FB and WML
low I limit R = (α/kd0.5) I
high I limit R = (α/(ψ2φ)0.5) I 0.5 Ithr = kd/(ψ2φ)
4 mW 80 mW1 µm 19.5 m2g-1
42.4 m2g-1100 nm
CH3COOH + 2O2 → 2CO2 + 2H2O
singularity!
★★
★
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89
ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
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90
electrochemical equilibrium = simultaneous front/backward
n -electron transfer
nnumber of electrons
digital!
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91
2H2O + 4h+ → 4H+ + O2 4 1.23 V
2H2O + 2h+ → 2H+ + H2O2 1.76 VH2O2 + 2h+ → 2H+ + O2 2 0.70 V
H2O + h+ → H+ + HO・ 2.8 VHO・ + h+ + H2O → H+ + H2O2 1 1.14 V
H2O2 + h+ → H+ + HO2・ 1.51 VHO2・ + h+ → H+ + O2 (n ) -0.13 V
possible oxygen liberation processes
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92
so-called "band-structure" model of photocatalysis
CB
VBh
e
How one SEP is chosen?
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93
special orbital overlapping=
(no change in position)
+ energy overlapping=
(no change in energy)
photoexciation
electron transfer
both depends on
surface orbitals
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singularity in a chemical reaction
related to particle sizedue to digitally controlled kinetics of
multielectron transfer
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95
so-called "band-structure" model of photocatalysis
CB
VBh
e
h+
e-
SEP/標準電極電位standard electrode
potential
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96
ETDOSMETSEP
density-of-states (DOS)distribution
standard electrode potential
multielectron transfer = number of electrons
identification with electron-trap distribution
to go beyond the band-structure model
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Advanced Course in Environmental Catalytic Reaction Chemistry I 97
format
Please send email in Japanese or English within 72 hoursto: [email protected]: pc2020MMDD-XXXXXXXX
[email protected](full name)(nickname)(what is learnt in this lecture series) + (questions if any)[blank line](answer for question 1)(answer for question 2)(answer for question 3)・・
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Advanced Course in Environmental Catalytic Reaction Chemistry I 98
email example
to
subject
(same as subject)email addressfull namenicknamecomment(s) +
question(blank line)answer 1answer 2answer 3・・
pc20200813-57388301
pc20200813-57388301
pc20200813-57388301
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Advanced Course in Environmental Catalytic Reaction Chemistry I 99
special report (20 + α points)
special report for extra (bonus) score (20 point)report on critical review on "photocatalysis" in Wikipedia, pointing out errors, misunderstanding and speculationsbased on the contents of this lecture.http://en.wikipedia.org/wiki/Photocatalysishttp://ja.wikipedia.org/wiki/光触媒
• Japanese or English• A4 size 2 pages• submission by email attachment• a PDF file is more preferable than a Word file• email title: pc20200820-XXXXXXXX• file name: pc20200820-XXXXXXXX.pdf (or .docx or .doc)• deadline of submission: August 20, 2020 23:59
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集合写真!group photo