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      SCOPUS SCIE

      Electrolysis of urea and urine for solar hydrogen

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      https://www.riss.kr/link?id=A107609155

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      Hybrid photovoltaic (PV) arrays-electrochemical systems have been envisaged as an alternative technology that co-manages an energy-water nexus, yet improving the technical viability and applicability of the hybrids remains a challenge. With this in mi...

      Hybrid photovoltaic (PV) arrays-electrochemical systems have been envisaged as an alternative technology that co-manages an energy-water nexus, yet improving the technical viability and applicability of the hybrids remains a challenge. With this in mind, we studied the hybrid electrochemical system for urea and urine treatment and simultaneous H<SUB>2</SUB> production using BiO<SUB>x</SUB>-TiO<SUB>2</SUB> anode and stainless steel cathode couples with different electrolytes (NaCl vs. LiClO<SUB>4</SUB> vs. Na<SUB>2</SUB>SO<SUB>4</SUB>). In the presence of NaCl, urea electrolysis was found to enhance the cathodic H<SUB>2</SUB> production by a maximum of ca. 20% at low urea concentrations, yet reduce the H<SUB>2</SUB> production at high urea concentrations as compared to water electrolysis. Varying degrees of the synergistic H<SUB>2</SUB> production were attributed to competitive reactions between active chlorine species and urea/urea intermediates for protons and electrons. The synergistic effect by the urea electrolysis disappeared when LiClO<SUB>4</SUB> and Na<SUB>2</SUB>SO<SUB>4</SUB> were used as electrolytes indicating the crucial role of chlorine species in the hybrid reactions. In addition, the electrolysis of actual urine was found to successfully operate along with simultaneous generation of H<SUB>2</SUB> even in the absence of externally added electrolytes. This electrolyteless-hybrid electrolysis resulted from the large amounts of chloride and other ionic species originally included in the actual urine sample. A detailed reaction mechanism of urea electrolysis and its application potential in terms of solar hydrogen were discussed.

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