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In the photoelectrochemical cell, it is not clear whether oxygen is present or removed from water solution? Should make a statement about this.

Dissolved oxygen can be readily reduced by the photoelectrons and thus must be considered. The V-I scan does not show the reverse scan results which might be indicative of the mechanism. (Õâ¾ä»°¸öÈËÀí½âÊÇ£¬ÈܽâÑõÈÝÒ×±»¹âµç×ÓÏûºÄ£¬Ó¦¸Ã¿¼ÂÇÓ°Ïì,Òª¼ÓÈë·´ÏòɨÃèÒÔ֤ʵÈܽâÑõ´æÔÚ)

What are the plausible chemical reactions that cause the photocurrents?
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By calculating efficiencies for water splitting, we are asked to assume that the reduction reaction is hydrogen evolution and the oxidation reaction is oxygen evolution. Dissolved oxygen can be reduced or Ag nanoparticles can be oxidised quite plausibly? Thus the current efficiency calculations while offering comparison between different samples, the actual numbers may not be meaningful, as 1.23V in the formula is an arbitrary choice. £¨Õâ¸ö¼ÆËãʽÓõÄÊǺó±ßÎÄÏ×Öеģ¬Ò»ÑùµÄʵÑé²ÎÊý²âÊÔ·½·¨£¬µ«ÊÇÉó¸åÈË˵ÓÃÕâ¸ö·½·¨¶Ô±È²»Í¬µÄÑùÆ·ÓÐÎÊÌ⣬²¢ÇÒ»¹ÖÊÒÉ1.23VµÄȡֵ£¬Õâ¸öÎÒ²éÁ˺ü¸ÆªÎÄÏ×¶¼ÊÇÀàËÆµÄÎÄÕÂËûµÄËã·¨ºÍȡֵ£¬1.23VÊÇÒ»¸ö¹Ì¶¨µÄȡֵ£¬¾ßÌå¿É²Î¿¼¸½¼þµÄÎÄÏ×£©

The V-I scan do not show peaks one may expect for hydrogen and oxygen evolutions? The potential window may not be sufficient?£¨»¹ÊÇÒ»ÑùµÄÎÊÌ⣬˵ûÓÐÔÚLSVɨÃèÖгöÏÖÑõ»¯»¹Ô­·å.µ«ÊÇÎҲ鵽µÄÎÄÏ×ÖеÄLSVµÃµ½µÄJ-VÇúÏß¶¼Ã»ÓÐʲô·å³öÏÖ°¡£¬µçÁ÷µÄ´óСֻÊÇΪÁ˶Աȷ´Ó³²»Í¬ÑùÆ·¹âµç»¯Ñ§ÐÔÄܵĺûµ¶øÒÑ£©

Using the impedance data, did the authors calculate the capacitance assocaited with the max loss for each of the 2 semi-circles to check whether the values can be readily ascribed to charge transfer resistances at the Pt RE and at the TiO2 WE. The first high frequency semicircle is ascribed to the Pt RE, hence the Capacitance values will turn out to be lower than that for the WE? Why should this be the case?
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ÆäÖеĹâµç»¯Ñ§ÊµÑéÊDzο¼ÎÄÏס°Controlled Sn-Doping in TiO2 Nanowire Photoanodes with Enhanced Photoelectrochemical Conversion¡± Nano Lett. 2012, 12, 1503¨â508   dx.doi.org/10.1021/nl2042968 .
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