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Tin sulfide SnS

Fig. 5.2 The n-Cd(Se,Te)/aqueous Cs2Sx/SnS solar cell. P, S, and L indicate the direction of electron flow through the photoelectrode, tin electrode, and external load, respectively (a) in an illuminated cell and (b) in the dark. For electrolytes, m represents molal. Electron transfer is driven both through an external load and also into electrochemical storage by reduction of SnS to metaUic tin. In the dark, the potential drop below that of tin sulfide reduction induces spontaneous oxidation of tin and electron flow through the external load. Independent of illumination conditions, electrons are driven through the load in the same direction, ensuring continuous power output. (Reproduced with permission from Macmillan Publishers Ltd [Nature] [60], Copyright 2009)... Fig. 5.2 The n-Cd(Se,Te)/aqueous Cs2Sx/SnS solar cell. P, S, and L indicate the direction of electron flow through the photoelectrode, tin electrode, and external load, respectively (a) in an illuminated cell and (b) in the dark. For electrolytes, m represents molal. Electron transfer is driven both through an external load and also into electrochemical storage by reduction of SnS to metaUic tin. In the dark, the potential drop below that of tin sulfide reduction induces spontaneous oxidation of tin and electron flow through the external load. Independent of illumination conditions, electrons are driven through the load in the same direction, ensuring continuous power output. (Reproduced with permission from Macmillan Publishers Ltd [Nature] [60], Copyright 2009)...
Tin in ambient waters may exist as divalent cationic (positively charged) ions (Sn ) or as quadrivalent ions (Sn +). Stannous tin (Sn ) dominates in reduced (oxygen-poor) water, and will readily precipitate as a sulfide (SnS) or as a hydroxide (Sn(OH)2) in alkaline water. Stannic tin (Sn ) readily hydrolyzes, and can precipitate as a hydroxide (Wedepohl et al. 1978). The solubility product of Sn(OH)4 has been measured as approximately 10 g/L at 25°C (Wedepohl et al. 1978). [Pg.136]

The presence of early transition metals or rare earth elements is not necessary for the stabilization of metal-rich compounds. This is shown by the metal-rich nickel-tin sulfides Ni6SnS2 and Ni9Sn2S2, which were found during investigations of phase relations in the ternary Ni-Sn-S... [Pg.720]

Cadmium sulfide, CdS Copper(II) sulfide, CuS Iron(II) sulfide, PeS Lead(II) sulfide, PbS Manganese(II) sulfide, MnS Mercury(II) sulfide, HgS Nickel(II) sulfide, NiS Silver sulfide, Ag2S Tin(II) sulfide, SnS Zinc sulfide, ZnS... [Pg.809]

Bis(triphenyltin)dihydridobis(methyldiphenylphosphine)plati-num, see Sn-00474 Bis(triphenyltin)oxide, see Sn-00440 >Bis(triphenyltin) sulfide, Sn-00443 Bis(triphenyltin)telluride, Sn-00446 >Bis(tripropyltin) oxide, see Sn-00339 >Bis[tris(2-methyl-2-phenylpropyl)tin] oxide, see Sn-00473 Bis[tris(pentafluorophenyl)germyl]cadmium, Ge-00271 Bis[tris(pentafluorophenyl)germyl] mercury, Ge-00273 Bis[tris(pentafluorophenyl)germyl] selenide, see Ge-00275 Bis[tris(pentafluorophenyl)germyl] sulfide, see Ge-00274 [Bis[tris(pentafluorophenyl)stannyl]]mercury, Sn-00435 Bis[tris(trifluoromethyl)germanium]oxide, see Ge-00064 Bis[tris[(trimethylsilyl)methyl]stannyl]mercury, Sn-00399 Bromo( 7 -2,4-cyclopentadien-1 -yl)lead, Pb-00035 Bromo( 7 -2,4-cyclopentadien-1 -yl)tin, Sn-00086 Bromodimethylstannane, Sn-00022... [Pg.139]

See other pages where Tin sulfide SnS is mentioned: [Pg.121]    [Pg.200]    [Pg.1174]    [Pg.477]    [Pg.25]    [Pg.210]    [Pg.121]    [Pg.200]    [Pg.1174]    [Pg.477]    [Pg.25]    [Pg.210]    [Pg.56]    [Pg.58]    [Pg.51]    [Pg.122]    [Pg.43]    [Pg.357]    [Pg.58]    [Pg.2636]    [Pg.4892]    [Pg.561]    [Pg.291]    [Pg.291]    [Pg.314]    [Pg.666]    [Pg.805]    [Pg.379]    [Pg.2635]    [Pg.4891]    [Pg.28]    [Pg.1324]    [Pg.1280]    [Pg.275]    [Pg.1316]    [Pg.1063]    [Pg.308]    [Pg.1104]    [Pg.77]    [Pg.77]    [Pg.79]    [Pg.43]    [Pg.736]    [Pg.637]    [Pg.805]    [Pg.226]    [Pg.590]    [Pg.141]   
See also in sourсe #XX -- [ Pg.2 , Pg.26 , Pg.30 ]



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