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Nitrogen Nanobubbles in a-SiOxNy Coatings: Evaluation of Its Physical Properties and Chemical Bonding State by Spatially Resolved Electron Energy-Loss Spectroscopy

Abstract

Nanoporous silicon-based materials with closed porosity filled with the sputtering gas have been recently developed by magnetron sputtering. In this work the physical properties (density and pressure) of molecular nitrogen inside closed pores in a SiOxNy coating are investigated for the first time using spatially resolved electron energy-loss spectroscopy (EELS) in a scanning transmission electron microscope. The paper offers a detailed methodology to record and process multiple EELS spectrum images (SIs) acquired at different energy ranges and with different dwell times. An adequate extraction and quantification of the N–K edge contribution due to the molecular nitrogen inside nanopores is demonstrated. Core-loss intensity and N chemical bond state were evaluated to retrieve 2D maps revealing the stable high density of molecular nitrogen (from 40 to 70 at./nm3) in nanopores of different size (20–11 nm). This work provides new insights into the quantification of molecular N2 trapped in porous nitride matrices that could also be applied to other systems.

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Nitrogen Nanobubbles in a-SiOxNy Coatings: Evaluation of Its Physical Properties and Chemical Bonding State by Spatially Resolved Electron Energy-Loss Spectroscopy

Author: Lacroix, Bertrand; Fortio Godinho, Vanda Cristina; Fernández Camacho, Asunción
Publisher: American Chemical Society
Year: 2016
DOI: 10.1021/acs.jpcc.5b09036
Source: https://idus.us.es/bitstreams/98acdae3-979e-4a6b-aca6-3f6c9d50c839/download
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1
Ni ogen Nanobubbles in a-SiO
x
N
y
Coa ings: E alua ion o i s Physical P ope ies and
Chemical Bonding S a e by Spa ially Resol ed EELS
Be and Lac oix*, Vanda Godinho, and Asunción Fe nández*
Ins i u o de Ciencia de Ma e iales de Se illa, CSIC - Uni e sidad de Se illa
A . Amé ico Vespucio 49, 41092 Se ille, Spain
ABSTRACT
Nanopo ous silicon based ma e ials wi h closed po osi y illed wi h he spu e ing gas ha e
been ecen ly de eloped by magne on spu e ing. In his wo k he physical p ope ies
(densi y and p essu e) o molecula ni ogen inside closed po es in a SiO
x
N
y
coa ing a e
in es iga ed o he i s ime using spa ially esol ed elec on ene gy-loss spec oscopy (EELS)
in a scanning ansmission elec on mic oscope. The pape o e s a de ailed me hodology o
eco d and p ocess mul iple EELS spec um images (SIs) acqui ed a di e en ene gy anges
and wi h di e en dwell imes. I is demons a ed an adequa e ex ac ion and quan i ica ion o
he N-K edge con ibu ion due o he molecula ni ogen inside nanopo es. Co e-loss in ensi y
and N chemical bond s a e we e e alua ed o e ie e 2D maps e ealing s able high densi y o
molecula ni ogen ( om 40 o 70 a ./nm
3
) in nanopo es o di e en size (20 o 11 nm). This
wo k p o ides new insigh s on he quan i ica ion o molecula N
2
apped in po ous ni ide
ma ices ha could be also applied o o he sys ems.
I. INTRODUCTION
Silicon based ma e ials a e s ill nowadays key o he de elopmen o mode n
echnology. Al hough signi ican basic esea ch has been unde aken in he ecen decades,
he esea ch in silicon oxyni ide (SiO
x
N
y
) coa ings is s ill a opic o high in e es .
1-4
The abili y
o modeling he op ical and elec ical p ope ies by con olling he composi ion makes o
SiO
x
N
y
a p omising ma e ial o op oelec onic de ices.
5-7
A con inuous change in i s
composi ion allows la ge e ac i e index anges om 1.47 o pu e silicon dioxide up o 2.3 o
pu e silicon ni ide o e en 4.75 o dense amo phous silicon coa ings
8
which is e y appealing
o low and high con as index applica ions.
Among o he deposi ion echniques SiO
x
N
y
coa ings a e mos commonly g own by
plasma enhanced chemical apo deposi ion. Composi ional changes a e achie ed by a ying
ni ous oxide (N
2
O) and silane (SiH
4
/N
2
) p ecu so a ios wi h op ional addi ion o ammonia
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2
(NH
3
). Howe e , he high hyd ogen con en in hese plasma-enhanced chemical apo
deposi ion ilms in he o m o Si-H o N-H bonds causes op ical losses a wa eleng hs a ound
1500nm.
3-4, 9
Addi ional
annealing s eps be ween 1000 and 1150°C, o plasma ea men s a
300°C ha e been p oposed o educe he H con en
3-4, 10
howe e limi ing he ype o
subs a es o be used.
We ha e ecen ly in oduced a new bo om up me hodology o p oduce silicon based
po ous coa ings wi h con olled e ac i e index by magne on spu e ing.
8, 11-13
This new
app oach gi es he possibili y o ob ain ailo ed mic os uc u es and e ac i e indexes based
on he in oduc ion o closed po osi y, illed wi h he spu e ing gas, in coa ings p oduced by
magne on spu e ing.
8, 12, 14-15
SiO
x
N
y
coa ings wi h simila composi ion and ailo ed e ac i e
index
11-12
as well as pu e o doped po ous silicon laye s
8, 16
can be deposi ed wi hou he
inco po a ion o H. In addi ion o he ad an ages o easy scale-up o he magne on spu e ing
p ocess we ha e demons a ed he easibili y o p oducing silicon pho onic s uc u es by his
p ocedu e
16
on a wide a ie y o subs a es om polyme s o glass.
Simila closed po es mic os uc u es can be ound in ion-i adia ed o ion-implan ed
hin ilms
17-23
which ha e been poin ed ou as ab ica ion ou es o nanos uc u ed ma e ials
and su aces.
19-25
Gene ally hese mic os uc u es consis in ew po es si ua ed a a ce ain
dis ance om he su ace; while wi h ou me hodology, highly po ous s uc u es wi h uni o m
po osi y om he subs a e o he coa ings su ace a e deposi ed, in a wide ange o
hicknesses ( om 100 nm o ew mic ons). F om a undamen al poin o iew hese new
ma e ials wi h embedded po es, illed wi h he spu e ing gas, ep esen a new class o
nanocomposi e ma e ials p esen ing on demand op ical p ope ies in compa ison wi h he
ma ix ilm. To ully unde s and and con ol hese p ope ies and also o he s abili y and
in eg i y o he coa ings in possible applica ions, he physical pa ame e s (densi y, p essu e)
de ining he s a e o he gases inside he po es become an impo an issue.
In a ecen wo k we ha e in es iga ed he s a e o Helium gas inside he po es o
magne on spu e ed amo phous silicon ilms, by spa ially esol ed elec on ene gy-loss
spec oscopy (EELS).
15
Th ough hese 2D spec oscopic maps a he nanoscale, we ha e been
able o demons a e ha He is loca ed inside he nanopo es o he coa ings in a condensed
s a e, wi h densi ies as high as ens o He a oms/nm
3
and p essu e close o he GPa ange.
15
The way o measu e he He densi y consis ed in ex ac ing he in ensi y o he He-K edge
(loca ed a abou 23 eV) and doing he quan i ica ion by conside ing he ze o-loss in ensi y,
he inelas ic c oss-sec ion o He and he po e hickness .
15,18
The p essu e was hen e alua ed
using a sui able equa ion o s a e.
15
In p inciple, a simila app oach could be used o quan i y
o he elemen s apped inside po es, like ni ogen in ou case. Howe e , con a y o he case
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o nanobubbles o nanopo es illed wi h helium o which quan i ica ion has al eady been
achie ed in a ious s udies,
15, 18, 26-29
only a ew wo ks a emp ed o e alua e he N
2
densi y
and p essu e inside closed ca i ies.
30-32
Mos o hem we e done in a semi-quan i a i e way
based on he a ia ion o he N-K edge in ensi y o e he ni ide ma ix and o e he po e.
30-31
Indeed, he quan i ica ion o he ni ogen densi y inside small po es is a mo e challenging
p oblem han o helium. The main eason is ha he N-K edge posi ion is qui e a om he
elas ic peak and due o he limi ed dynamical ange o he CCD de ec o s, he low-loss (LL) and
co e-loss (CL) ene gy ange ha e o be eco ded sepa a ely, wi h di e en dwell imes.
33
To ou
knowledge, only one wo k o he li e a u e
32
has epo ed he quan i ica ion o ni ogen
densi y om EELS based on Re . 18, bu e y ew de ails o he analysis we e gi en (in
pa icula he way o eco d and p ocess he EELS da a o ge he ze o-loss and N-K edge
in ensi ies). In addi ion, his s udy was pe o med on an ideal case wi h a su ounding ma ix
ee o ni ogen.
In his con ex , his a icle p esen s o he i s ime he ex ac ion o he N-K signal
due o molecula ni ogen and he quan i ica ion o he densi y and p essu e o N
2
condensed
inside small po es su ounded by an oxyni ide ma ix. The LL and CL EELS spec um images
we e acqui ed consecu i ely and ha e been p ocessed ollowing he ecen wo k by Bobynko
e al. in Re . 34. A be e app oach would ha e been o use he so-called DualEELS echnique
(no a ailable in ou s udy). Howe e , as an al e na i e o DualEELS, we sugges he e o
acqui e he LL and CL SIs sepa a ely and o ealign hem spa ially du ing a pos p ocessing s ep.
Ou s udy will ocus on nanopo es illed wi h N
2
and o med in SiO
x
N
y
ilms deposi ed by
magne on spu e ing acco ding o ou p e ious wo k.
11-12
Howe e , his app oach may also be
gene alized o allow o s udy o he sys ems, including ni ide ma e ials, and con aining ca i ies
illed wi h molecula ni ogen ei he o med du ing syn hesis
30-31, 35-36
o nanos uc u ing
p ocesses like ion i adia ion o implan a ion.
19, 22-23
Finally a compa ison wi h mac oscopic
esul s ob ained p e iously om Ru he o d backsca e ing spec ome y (RBS) measu emen s
will be p esen ed o con i m ou EELS quan i ica ion a he nanoscale.
II. EXPERIMENTAL METHODS
In o de o ha e closed po osi y illed wi h N
2
, he SiO
x
N
y
coa ing chosen o his s udy
was deposi ed on Si (100) subs a e, as desc ibed in Re . 12, by eac i e magne on spu e ing
using a mix u e o ni ogen and oxygen as spu e ing gas ( o al p essu e o 1.33 Pa, oxygen
pa ial p essu e o 1x10
-4
Pa). A RF powe sou ce a 150 W was used o spu e a pu e Si a ge
(Ku J. Leske 99.999%). To ob ain he la ges po es acco ding o ou p e ious wo k,
12
he
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sample holde was placed a a dis ance o 10 cm om he magne on head (2” ION’X
magne on om Thin Film Consul ing, Ge many).
T ansmission elec on mic oscopy (TEM) expe imen s we e ca ied ou a he
Ad anced Labo a o y o Nanoscopies and Spec oscopies-LANE a he ICMS (Se ille, Spain)
using a FEI Tecnai F30 mic oscope ope a ed a 300 keV. C oss-sec ional TEM specimens we e
p epa ed by mechanical polishing and dimple g inding ollowed by A gon ion milling, un il
elec on anspa ency was achie ed. Jus be o e inse ion in o he TEM, he specimen inside
he holde was cleaned in O
2
/A plasma. The coa ing mo phology was s udied by con en ional
b igh ield (BF) and high esolu ion TEM (HRTEM) imaging. To analyze he ma ix and po es
composi ion, elec on ene gy-loss spec oscopy spec um images (EELS-SIs) we e eco ded
wi h a GATAN GIF Quan um ene gy il e using he scanning TEM high-angle angula da k ield
(STEM-HAADF) mode. The EELS spec a we e eco ded o e 2048 channels wi h a dispe sion o
0.25 eV/channel. The con e gence and accep ance semi-angles we e se o 12.4 m ad and 9.6
m ad, espec i ely and he p obe cu en anged be ween 50 and 90 pA. In o de o measu e
he densi y o ni ogen apped inside he po es, EELS-SIs we e eco ded consecu i ely in he
CL and LL anges, wi hin a ew minu es o in e al. The ene gy anges used o eco d he da a
( om -50 o 462 eV o he LL, and om 210 o 722 eV o he CL) we e se o ge a su icien
numbe o channels o o e lapping ene gies o subsequen escaling. Elec on p obe spacing
o 1 o 3 nm wi h subpixel scanning (16x16) was used and di e en in eg a ion imes in bo h
anges we e se o a oid signal sa u a ion on he CCD ( ypical alues a e 0.5 second/spec a o
he CL and 0.02 second/spec a o he LL). The ene gy esolu ion o 1.5 eV was de e mined a
he ull wid h a hal maximum o he elas ic peak. Du ing he acquisi ion, spa ial d i
co ec ion was applied and he EELS da a we e co ec ed o he da k cu en and he gain
a ia ion o he CCD de ec o . Da k cu en co ec ion was imp o ed a e each SI acquisi ion
using he unc ion p o ided by he GATAN Mic oscopy Sui e 2.1.
The ilm bulk composi ion was de e mined by RBS using he 3 MV andem accele a o
o he Na ional Cen e o Accele a o s in Se ille (Spain). The spec a we e measu ed wi h a 2
MeV He
+
beam and he de ec ion angle was 165°. The expe imen al spec a we e analyzed
using he SIMNRA simula ion code.
37
III. RESULTS AND DISCUSSION
Mic os uc u e, bonding and composi ional in o ma ion o he coa ing
Fo his s udy a pa icula po ous silicon oxyni ide coa ing wi h a bulk composi ion
Si:O:N = 35:20:45 a . % as gi en by RBS, p esen ing 26% o po osi y and a e ac i e index o
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5
1.60 was selec ed (mo e de ailed cha ac e iza ion o his coa ing is p esen ed in p e ious
wo ks
11-12
).
The BF TEM image in Fig. 1a p esen s an o e iew o he SiO
x
N
y
coa ing mic os uc u e
whe e he po ous s uc u e can be seen in b igh con as . Po es om abou 3 o 20 nm in size
a e obse ed. In he high magni ica ion image shown in Fig. 1b i is possible o obse e in mo e
de ail he ound shape o he po es and he absence o c ys al plane ea u es.
The Si-L, N-K, and O-K edges p o ide use ul in o ma ion on he bonding s a e o hese
elemen s in he SiO
x
N
y
ma ix and con i m he p esence o molecula N
2
inside he po es.
Figu e 1c shows he ene gy-loss nea -edge s uc u es (ELNES) eco ded ac oss he ma ix and
ac oss one po e compa ed o e e ence edges o amo phous SiO
2
,
38
Si
3
N
4
,
39
as well as O
2
40
and
N
2
41
. These ELNES we e ex ac ed om he singula sca e ing dis ibu ion by i ing he signal
p io o he edge wi h a powe -law unc ion. P io o he edge ex ac ion, he EELS-SIs we e
p ocessed ollowing he p ocedu e desc ibed la e in his wo k. As can be obse ed in Fig. 1c.1,
he Si-L edges o he ma ix and po e egions exhibi simila shapes, wi h ou main ea u es
labelled `a1´, `a2´, `a3´ and `a4´ a abou 105 eV, 113 eV, 127 eV, and 156 eV, espec i ely.
Such ea u es a e closed o he Si
3
N
4
e e ence and hus indica e ha Si-N bonds domina e in
he p esen SiO
x
N
y
coa ing. In SiO
2
, hese ea u es a e sligh ly shi ed owa ds he highe
ene gies. The e o e, he la ge peak wid hs obse ed o SiO
x
N
y
may also indica e he p esence
o Si-O bonds. The O-K ELNES eco ded ac oss he po e and he ma ix does no p esen
signi ican di e ences (Fig. 1c.3). The spec a p esen wo main ea u es iden i ied as `c2´ and
`c3´ a abou 538 eV and 560 eV and ha e s ong simila i ies wi h he SiO
2
e e ence, which
indica es ha oxygen a oms ha e simila local a omic en i onmen han in silica. The shape o
N-K edge changes signi ican ly wi h he posi ion o he elec on p obe (Fig. 1c.2). Ac oss he
ma ix, he ELNES is e y simila o he inge p in in Si
3
N
4
, wi h wo main b oad ea u es `b2´
and `b3´ a 405 eV and 422 eV. In he po e a ea an addi ional in ense na ow peak `b1´
appea s a he onse a ound 401 eV, co esponding o he signa u e o molecula ni ogen N
2
as obse ed p e iously in Re . 12. These da a con i m ha he po es a e illed wi h molecula
ni ogen.
The composi ion o he SiO
x
N
y
ma ix has been de e mined om hese edges using he
Digi al Mic og aph p og am. Acco ding o Re . 42, an in eg a ion window o 25 eV was se o
Si-L, while he N-K and O-K edges we e in eg a ed o e 100 eV. An a e age ma ix composi ion
Si:O:N 33:25:42 a . % was calcula ed using Ha ee-Sla e c oss-sec ions. I is wo h o no e
ha he composi ion ob ained by quan i ica ion o he EELS spec a o he ma ix is in qui e
good ag eemen wi h he bulk composi ion o he coa ing measu ed p e iously by Ru he o d
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backsca e ing spec oscopy. The alue o he ma ix composi ion by EELS quan i ica ion will
be used la e o calcula e he inelas ic mean ee pa h o elec ons in he specimen.
EELS-SI da a p ocessing o composi ional analysis
The nex sub-sec ions desc ibe he s eps necessa y o p ocessing he da a in o de o
quan i y he N
2
densi y inside he po es su ounded by he amo phous oxyni ide ma ix. An
Ad hoc semi-au oma ed code unning wi h MATLAB has been de eloped o allow he da a
analysis o e la ge da ase s. I is a ailable on demand. P io o he analysis, X- ays spikes we e
emo ed om he SIs using he ou ine p o ided wi h he GATAN Mic oscopy Sui e 2.1.
Spa ial and ene gy alignmen o he SIs and noise educ ion
Since he LL and CL EELS-SIs we e eco ded sepa a ely, o ensu e ha each pixel o he
wo EELS-SIs co esponds o he same specimen a ea, he wo da ase s we e i s ealigned
spa ially. Fo ha pu pose, he STEM-HAADF images eco ded in he low-loss and he co e-loss
anges we e used as e e ences and submi ed o c oss-co ela ion. Mo e in o ma ion abou
he spa ial alignmen o he LL and CL da ase s can be ound in he Suppo ing In o ma ion.
In a second s ep, he da ase s we e ealigned along he ene gy axis. Figu e 2a shows
he STEM-HAADF signal o he po ous coa ing acqui ed in pa allel wi h EELS spec um images.
On his image, he in ensi y is p opo ional o he a omic numbe and he hickness o he
sample, he da k a eas co espond o phases wi h lowe Z, and in his case he po es a e
da ke han he su ounding ma ix. Figu es 2b-d p esen wo examples o LL and CL spec a
eco ded ac oss he ma ix and ac oss one po e a e he alignmen p ocedu e. In he LL ange,
he spec a we e shi ed in o de o ge o each pixel posi ion he ze o-loss peak (ZLP) a he
same channel co esponding o ze o ene gy-loss (Fig. 2b). On Fig. 2b, he bulk plasmon can be
seen a abou 22.6 eV. An addi ional peak a ound 14 eV, a ibu ed o he ca i y plasmon,
28, 43
is also obse ed when he p obe is loca ed ac oss he po e. An addi ional b oad ea u e can be
obse ed be ween 15 o 19 eV, which can be en a i ely a ibu ed o su ace s a es o he
SiO
x
N
y
ma ix. This ea u e is mo e impo an in he po es egions whe e he ma ix laye is
hinne han in he bulk ma ix. The Si-L edge also appea s in he LL ange nea 100 eV, see Fig.
2c. Howe e , he N-K edge a ound 400 eV is no isible on he LL spec a due o he low
exposu e ime. In he CL ange, he spec a we e shi ed by aligning he onse o he O-K edge
a e e ence ene gy o 532 eV. Figu e 2d clea ly shows he N-K edge, whose signa u e depends
on he posi ion o he elec on p obe: ou side he po es, he N-K edge p esen s he wo b oad
bands ypical o he SiO
x
N
y
ma ix
12
whe eas he signal eco ded ac oss he po e has an
addi ional na ow peak a he onse (401 eV) which is a ibu ed o molecula ni ogen N
2
.
12
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7
The choice o O-K ins ead o N-K as e e ence edge o he alignmen was mo i a ed by he
ac ha i s shape emains unchanged wha e e he posi ion o he p obe is.
As can be obse ed on he blue cu es o Fig. 2, he EELS spec a con ain a subs an ial
noise componen ha can a ec he backg ound sub ac ion o u he quan i ica ion. In
o de o educe his con ibu ion, p incipal componen analysis (PCA)
44
was applied on he LL
and CL HL da ase s a e he alignmen s ep. The signal was hen econs uc ed wi h a g ea
ca e o a oid he loss o ele an spec oscopic in o ma ion by keeping a limi ed (bu
su icien ly la ge) numbe o componen s, as shown on he ed plo s on Fig. 2. Mo e de ails on
PCA a e gi en in he Suppo ing In o ma ion.
Splicing o he LL and CL spec a and mul iple sca e ing decon olu ion
As he LL and CL EELS da a we e eco ded wi h di e en exposu e imes, he nex s ep
consis s in splicing he spec a oge he pixel-by-pixel. This s ep has been pe o med wi h
special ca e because esidual noisy signal in he LL splicing egion (due o low exposu e ime)
may in oduce addi ional e o s in he de e mina ion o he scaling ac o . An example o
spliced spec um and addi ional de ails ela ed o he splicing p ocedu e a e gi en in he
Suppo ing In o ma ion.
Elec on mul iple sca e ing can s ongly a ec he shape o he ene gy-loss nea -edge
s uc u es (ELNES) especially when he specimen hickness inc eases.
45
In he case o po ous
ma e ial wi h po es o se e al nm in size, changes in he specimen hickness c ossed by he
elec on beam occu . In o de o compa e he edge shapes and in ensi ies o di e en
posi ion o he p obe, i is necessa y o emo e hese plu al sca e ing e ec s. Fo ha
pu pose, mul iple sca e ing decon olu ion was applied o he spliced spec a using he Fou ie
loga i hmic me hod (see FLOG ou ine in Re . 45). An example o spec um ob ained a e
decon olu ion is p o ided in he Suppo ing In o ma ion.
Quan i ica ion o molecula ni ogen inside he po es
In o de o sepa a e he wo o e lapping signals coming om he ma ix and om
po es, he N-K edges we e be o ehand ex ac ed om he decon olu ed spec a by i ing he
signal p io o he edge wi h a powe -law unc ion. Figu e 3a illus a es he ex ac ion
p ocedu e o he N
2
componen . An a e age con ibu ion o he ma ix was i s de e mined
om a se o pixels ou side he po e egions. The ma ix spec um was hen scaled up o
ma ch he in ensi y o each ex ac ed N-K edge spec um in he da ase . To ind he adequa e
scale ac o , leas squa e i ing was pe o med in wo egions: be o e he edge (390 - 398 eV),
and be ween 403.5 and 405.8 eV whe e he con ibu ion o he molecula ni ogen o he N-K
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edge spec um is closed o ze o. The scaled SiO
x
N
y
ma ix con ibu ion was inally emo ed o
ob ain he molecula ni ogen componen . In Fig. 3a, one can no ice ha he shape o he
molecula con ibu ion ex ac ed om ou sample is simila o he N
2
e e ence om McLa en
e al.
41
Mo eo e , he N
2
con ibu ion is negligible ou side he po e while i is e y s ong
ac oss he po e, as expec ed. A con ibu ion o he ma ix is s ill p esen due o he SiO
x
N
y
walls su ounding he closed po e. All hese obse a ions allow us o alida e ou ex ac ion
p ocedu e. This app oach was pe o med pixel-by-pixel and he in ensi ies we e in eg a ed
o e 100 eV o e u n a 2D map ep esen ing he spa ial dis ibu ion o each componen . As
can be seen on Fig. 3b, he amoun o molecula ni ogen ac oss he po e a ea is closed o 50%
(blue egion) indica ing he p esence o a high N
2
con en .
The densi y o molecula ni ogen inside he po es 

can now be e alua ed om an
app oach simila o ha in oduced in Re . 18 using:


=





ℎ(1)
In equa ion (1), 

ep esen s he in eg al in ensi y o he molecula con ibu ion on he N-K
edge. 

is he angle-in eg a ed c oss-sec ion o he N-K edge. I was calcula ed in ou
expe imen al condi ions wi h he hyd ogenic model using he SIGMAK3 ou ine.
45
Bo h 

and


we e de e mined o e an ene gy ange o 100 eV s a ing a he edge onse . A la ge
in eg a ion window was chosen o a e age ou chemical bonding e ec s and maximize he
signal, as sugges ed by C ozie and Chenna
46
. The pa ame e ℎ is he local po e (o ca i y)
hickness c ossed by he elec on beam, which was de e mined as he complemen o he local
hickness measu emen s o he ma ix.
15, 26, 28
Fo ha pu pose, he absolu e specimen
hickness  was compu ed by combining he calcula ions o he ela i e specimen hickness /
wi h he inelas ic mean ee pa h . / was de e mined by he Log- a io me hod.
45
 was
ob ained using he pa ame ized app oach desc ibed by Malis e al.
47
aking in o accoun he
ma ix composi ion de e mined p e iously. As he highes sou ce o unce ain ies ce ainly
comes om he ℎ pa ame e , he po e hickness de e mina ion was c oss-checked wi h he
measu emen o he po e size  on he STEM-HAADF images assuming sphe ical po es. The
in eg al in ensi y o he elas ic peak 

was also de e mined and s o ed o each posi ion
du ing he calcula ion o ℎ.
Figu e 4 and Table I p esen he esul s ob ained on he la ges po e o he da ase
(Po e#1 in he able). The 2D maps in Fig. 4a-d ep esen he no malized HAADF in ensi y, /,


and 

alues. The ni ogen densi y map, shown in Fig. 4e, was calcula ed using 

=2427
ba n and  =161 nm. An a e age densi y 

=45 a oms/nm
3
was de e mined om a se o
pixels in he po e cen e , which co esponds o abou 23 N
2
molecules/nm
3
(1.04 g/cm
3
o
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FIGURES
FIG. 1. (a) BF TEM image o he SiO
x
N
y
coa ing showing he nanopo ous s uc u e (in b igh
con as ). (b) High magni ica ion image eco ded a he icini y o a ious po es. The image
was acqui ed in sligh unde - ocused condi ions in o de o see he con ou o he po es. (c)
ELNES eco ded ac oss he ma ix and ac oss he po e o he SiO
x
N
y
coa ing compa ed wi h
e e ences o Si
3
N
4
and SiO
2
, N
2
and O
2
(c.1) Si-L edge. (c.2) N-K edge. (c.3) O-K edge.
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FIG. 2. (a) STEM-HAADF image eco ded o e a ious po es (in da k con as ) simul aneously
wi h he EELS da a. Labels (1) and (2) indica e he pixels chosen o plo ing he aligned EELS
spec a eco ded ac oss one po e and ac oss he ma ix, be o e and a e PCA, in di e en
ene gy anges. (b) Low-loss ange wi h he ZLP and plasmons con ibu ions. (c) Middle-end o
he low-loss ange wi h he Si-L edge isible a abou 100 eV. (d) High-loss ange wi h he N-K
and O-K edges isible a abou 400 and 532 eV.
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FIG. 3. (a) Ex ac ion o he molecula con ibu ion om he N-K edge (ac oss he po e and
ac oss he ma ix). The g een a eas indica es he ene gy anges whe e he ma ix con ibu ion
was scaled o he N-K edge. The N
2
e e ence spec um shown o compa ison was ob ained
om Re . 41. (b) 2D map showing he a io o in ensi ies (in eg a ed o e 100 eV) o he wo N-
K componen s (molecula /ma ix).
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FIG. 4. 2D quan i ica ion o he molecula ni ogen inside one po e. (a) STEM-HAADF map, (b)
ela i e specimen hickness map, (c) ze o-loss in ensi y map, (d) molecula N-K in ensi y map,
(e) ni ogen a omic densi y map. Each pixel on he maps co esponds o 2 nm.
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FIG. 5. E olu ion o he molecula ni ogen densi y as a unc ion o he in e se o he po e
adius 1/ (wi h  = ℎ/2) assuming ha he po es a e sphe ical. The ed dashed line
ep esen s he linea i o he da a.
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FIG. 6. (a) E olu ion o he N-K edge eco ded in he cen e o a po e o di e en esidence
ime o he elec on p obe. EELS-SIs we e eco ded consecu i ely o e he same po e (abou
25 nm in size) using an in eg a ion ime o 0.5s/pixels. Fo compa ison pu pose, he edges
we e aken om he same pixel posi ion ac oss he po e and ex ac ed by powe -law i ing.
Excep he use o a dispe sion o 0.1 eV/channel, he o he expe imen al condi ions a e simila
o ha p esen ed in Sec. II. The esidence ime o he p obe was de e mined as he numbe o
pixels eco ded ac oss he po e mul iplied by he in eg a ion ime pe pixel, as p oposed by
Da id e al. (Re . 29). (b) Va ia ion o he in eg al in ensi y o he N-K edge in he [399-403]eV
ange.
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TABLES
TABLE I. Ni ogen densi y and p essu e measu ed inside po es o di e en size. The po e size
ange  was de e mined om he HAADF images. The mean alues o ℎ, 

and 

we e
es ima ed om STEM-EELS analysis o e a se o pixels aken ac oss he po e cen e . The
e o s co espond o he s anda d de ia ion.
Po e

(nm)

(nm)


(a ./nm
3
)



(GPa)
#1
18
-
20.5
18 ±
2
45
±
3
0.8
#2
12
-
13.5
11
±
2
72
±
5
7.5
#3
13
-
14
14
±
2
69
±
6
6.3
#4
14
-
20
20
±
4
40
±
12
0.5
#5
11
-
15
16
±
2
59
±
10
2.8
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Table o Con en s (TOC)
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- 1 0 0 1 0 2 0 3 0 4 0 5 0 6 0 7 0
350 400 450 500 550 600
100 200 300 400
( 2 )
( d )( c )
a e a l i g n m e n
a e P C A
I n e n s i y ( a . u . )
E n e g y l o s s ( e V )
( a ) ( b )
( 1 )
p o e ( 1 )
m a i x ( 2 )
I n e n s i y ( a . u . )
E n e g y l o s s ( e V )
a e a l i g n m e n
a e P C A
p o e ( 1 )
m a i x ( 2 )
a e a l i g n m e n
a e P C A
I n e n s i y ( a . u . )
E n e g y l o s s ( e V )
p o e ( 1 )
m a i x ( 2 )
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