Letno poročilo 2005
Letno poročilo 2005
Letno poročilo 2005
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1 objavljeni znanstveni prispevek na<br />
konferenci (vabljeno predavanje)<br />
5 objavljenih znanstvenih prispevkov na<br />
konferencah<br />
15 objavljenih povzetkov znanstvenih<br />
prispevkov na konferencah<br />
1 patentna prijava<br />
3 kon~na poro~ila o rezultatih raziskav<br />
3 elaborati, pred{tudije, {tudije<br />
2 diplomi<br />
GLAVNI DOSE@KI V LETU <strong>2005</strong><br />
- Sinteza in karakterizacija novega materiala z<br />
bistveno ve~jo teoreti~no kapaciteto od doslej<br />
znanih materialov za pozitivne baterijske<br />
elektrode<br />
V doslej znanih materialih za pozitivne elektrode<br />
v litijevih baterijah smo lahko za shranjevanje<br />
energije izkoristili najve~ 1 litij na<br />
molekulsko enoto materiala – ~eprav je ta<br />
enota na~eloma lahko vsebovala ve~ kot 1<br />
litij. S tem je bila specifi~na kapaciteta pozitivnih<br />
elektrod omejena na vrednosti med 150<br />
in 170 mAh/g. V laboratoriju pa nam je uspelo<br />
sintetizirati povsem nov anorganski<br />
material, Li 2 MnSiO 4 , v katerem lahko za<br />
shranjevanje naboja teoreti~no izrabimo oba<br />
litija, kar pomeni, da zna{a teoreti~na kapaciteta<br />
okoli 320 mAh/g. @al v praksi zaenkrat<br />
te kapacitete nismo uspeli izkoristiti – pri<br />
praznjenju/polnjenju dobimo podobne vrednosti<br />
kapacitete kot v prej omenjenih klasi~nih<br />
materialih. Vzrok so takoreko~ izolatorske<br />
elektri~ne lastnosti silikatov (elektronska<br />
prevodnost za Li 2 MnSiO 4 denimo zna{a okoli<br />
10 -12 S/cm), kar upo~asni kinetiko do te mere,<br />
da v realnem ~asu lahko izkoristimo le del<br />
razpolo`ljivega naboja. Glede na pretekle<br />
izku{nje s podobnimi izolatorskimi materiali<br />
pa obstaja realna mo`nost, da bomo z ustreznimi<br />
modifikacijami (zmanj{evanjem<br />
povpre~ne velikosti delcev, dodajanjem<br />
prevodnih faz, morda celo z dopiranjem)<br />
precej izbolj{ali povpre~no prevodnost elektrodnega<br />
kompozita ter posledi~no izkoristili<br />
znatno ve~ kot 1 litij na molekulsko enoto<br />
Laboratorij za elektrokemijo materialov<br />
Laboratory for Materials Electrochemistry<br />
1 Published Scientific Conference Contribution<br />
(Invited Lecture)<br />
5 Published Scientific Conference Contributions<br />
15 Published Scientific Conference Contribution<br />
Abstracts<br />
1 Patent Application<br />
3 Final Research Reports<br />
3 Treatises, Preliminary Studies, Studies<br />
2 Undergraduate Theses<br />
IMPORTANT ACHIEVEMENTS IN <strong>2005</strong><br />
- Synthesis and characterization of a new material<br />
with a considerably higher theoretical<br />
capacity than in present materials for Li battery<br />
positive electrodes<br />
In all existing materials for positive Li electrodes<br />
it is only possible to reversibly exchange<br />
up to 1 lithium per formula unit – even if the<br />
formula contains more than 1 lithium. This<br />
has limited the specific capacity of positive<br />
electrodes to values between 150 and 170<br />
mAh/g. Recently we have synthesized a completely<br />
new inorganic compound, Li 2 MnSiO 4 ,<br />
in which both lithium ions can in principle<br />
be exchanged so that the theoretical reversible<br />
capacity amounts as high as 320 mAh/<br />
g. Unfortunately, in practice we have not<br />
been able to exploit this huge capacity. In<br />
fact, upon material cycling we have obtained<br />
similar values of capacity as reported for other<br />
materials. The reason is the huge electrode<br />
polarization resulting from the insulating<br />
nature of silicates (for example, the electronic<br />
conductivity of Li 2 MnSiO 4 is in the range of<br />
10 -12 S/cm) which limits the exploitation of<br />
available charge. However, based on our experience<br />
with other insulating active particles,<br />
we hope that in future we will be able<br />
to improve the average conductivity of electrode<br />
composites, either by particle size minimization,<br />
addition of conductive phases or<br />
even by heterogeneous doping. It can be<br />
claimed that eventual practical exploitation<br />
of more than 1 Li per formula unit will open<br />
a new chapter in search for high-energy density<br />
storage materials.<br />
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