ON THE MODIFICATION AND CHARACTERIZATION OF CHEMICAL SURFACE-PROPERTIES OF ACTIVATED CARBON - MICROCALORIMETRIC, ELECTROCHEMICAL, AND THERMAL-DESORPTION PROBES
Ja. Menendez et al., ON THE MODIFICATION AND CHARACTERIZATION OF CHEMICAL SURFACE-PROPERTIES OF ACTIVATED CARBON - MICROCALORIMETRIC, ELECTROCHEMICAL, AND THERMAL-DESORPTION PROBES, Langmuir, 13(13), 1997, pp. 3414-3421
Further insight into important aspects of the chemical surface propert
ies of activated carbons is provided by rationalizing the differences
in O-2 adsorption and desorption behavior of hydrogen- and nitrogen-tr
eated activated carbons. The effects of heat treatment on the electroc
hemical behavior of these carbons were also instrumental in elucidatin
g the nature and the distribution of carbon active sites, Activated ca
rbon surfaces stabilized with hydrogen at 950 degrees C adsorb very li
ttle O-2 L at room temperature but the graphene layers are terminated
with many free carbon active sites because significant O-2 adsorption
does take place at 150 degrees C. Furthermore, the low-coverage differ
ential heats of adsorption on sites accessible at 150 degrees C were l
ower than those on sites accessible at 25 degrees C. The role of these
free carbon sites in determining the basicity of activated carbons wa
s also addressed. On the basis of the important finding that the point
of zero charge exhibits a maximum at intermediate heat-treatment temp
eratures, it is proposed that-in addition to the delocalized basal-pla
ne pi electrons-the localized pi electrons at graphene edges (e.g., in
plane divalent sigma pairs) act as Lewis bases that interact with prot
ons in aqueous solution.