We demonstrate using single molecule spectroscopy that inorganic CsPbI3 perovskite quantum dots (PQDs) undergo an irreversible, photoaccelerated reaction with water that results in a blue-shift of the photoluminescence (PL) and ultimately to complete quenching of the emission. We find that decomposition does not take place in the presence of oxygen alone but that it requires light and water. We also analyze the blinking for some stable PQDs and find a continuous distribution of emission states with a linear correlation between intensity and lifetime. We postulate that, in addition to charging and discharging processes, blinking arises from the activation and deactivation of nonradiative recombination centers in the PQDs.

The carbon monoxide dehydrogenase was purified from Clostridium thermoaceticum to apparent homogeneity. The 120‐fold purified enzyme with app. M r 250000 had a nickel content of 10 ± 2 μmol Ni/protein.

Growth of Acetobacterium woodii on H2 and CO2 rather than on fructose was dependent on nickel. Nickel-deprived cultures growing on fructose did not synthesize acetate from CO2; under these conditions hydrogen formation was used as the electron sink. The data indicate that nickel is involved in CO2 reduction to acetate in A. woodii.

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