Unifying the Hydrogen Evolution and Oxidation Reactions Kinetics in Base by Identifying the Catalytic Roles of Hydroxyl-Water-Cation Adducts
Despite the fundamental and practical significance of the hydrogen evolution and oxidation reactions (HER/HOR), their kinetics in base remain unclear. Herein, we show that the alkaline HER/HOR kinetics can be unified by the catalytic roles of the adsorbed hydroxyl (OHad)-water-alkali metal cation (A...
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Veröffentlicht in: | Journal of the American Chemical Society 2019-02, Vol.141 (7), p.3232-3239 |
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container_title | Journal of the American Chemical Society |
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creator | Liu, Ershuai Li, Jingkun Jiao, Li Doan, Huong Thi Thanh Liu, Zeyan Zhao, Zipeng Huang, Yu Abraham, K. M Mukerjee, Sanjeev Jia, Qingying |
description | Despite the fundamental and practical significance of the hydrogen evolution and oxidation reactions (HER/HOR), their kinetics in base remain unclear. Herein, we show that the alkaline HER/HOR kinetics can be unified by the catalytic roles of the adsorbed hydroxyl (OHad)-water-alkali metal cation (AM+) adducts, on the basis of the observations that enriching the OHad abundance via surface Ni benefits the HER/HOR; increasing the AM+ concentration only promotes the HER, while varying the identity of AM+ affects both HER/HOR. The presence of OHad-(H2O) x -AM+ in the double-layer region facilitates the OHad removal into the bulk, forming OH–-(H2O) x -AM+ as per the hard–soft acid–base theory, thereby selectively promoting the HER. It can be detrimental to the HOR as per the bifunctional mechanism, as the AM+ destabilizes the OHad, which is further supported by the CO oxidation results. This new notion may be important for alkaline electrochemistry. |
doi_str_mv | 10.1021/jacs.8b13228 |
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M ; Mukerjee, Sanjeev ; Jia, Qingying</creator><creatorcontrib>Liu, Ershuai ; Li, Jingkun ; Jiao, Li ; Doan, Huong Thi Thanh ; Liu, Zeyan ; Zhao, Zipeng ; Huang, Yu ; Abraham, K. M ; Mukerjee, Sanjeev ; Jia, Qingying ; Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)</creatorcontrib><description>Despite the fundamental and practical significance of the hydrogen evolution and oxidation reactions (HER/HOR), their kinetics in base remain unclear. Herein, we show that the alkaline HER/HOR kinetics can be unified by the catalytic roles of the adsorbed hydroxyl (OHad)-water-alkali metal cation (AM+) adducts, on the basis of the observations that enriching the OHad abundance via surface Ni benefits the HER/HOR; increasing the AM+ concentration only promotes the HER, while varying the identity of AM+ affects both HER/HOR. The presence of OHad-(H2O) x -AM+ in the double-layer region facilitates the OHad removal into the bulk, forming OH–-(H2O) x -AM+ as per the hard–soft acid–base theory, thereby selectively promoting the HER. It can be detrimental to the HOR as per the bifunctional mechanism, as the AM+ destabilizes the OHad, which is further supported by the CO oxidation results. 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Herein, we show that the alkaline HER/HOR kinetics can be unified by the catalytic roles of the adsorbed hydroxyl (OHad)-water-alkali metal cation (AM+) adducts, on the basis of the observations that enriching the OHad abundance via surface Ni benefits the HER/HOR; increasing the AM+ concentration only promotes the HER, while varying the identity of AM+ affects both HER/HOR. The presence of OHad-(H2O) x -AM+ in the double-layer region facilitates the OHad removal into the bulk, forming OH–-(H2O) x -AM+ as per the hard–soft acid–base theory, thereby selectively promoting the HER. It can be detrimental to the HOR as per the bifunctional mechanism, as the AM+ destabilizes the OHad, which is further supported by the CO oxidation results. 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Advanced Photon Source (APS)</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Ershuai</au><au>Li, Jingkun</au><au>Jiao, Li</au><au>Doan, Huong Thi Thanh</au><au>Liu, Zeyan</au><au>Zhao, Zipeng</au><au>Huang, Yu</au><au>Abraham, K. M</au><au>Mukerjee, Sanjeev</au><au>Jia, Qingying</au><aucorp>Argonne National Lab. (ANL), Argonne, IL (United States). Advanced Photon Source (APS)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Unifying the Hydrogen Evolution and Oxidation Reactions Kinetics in Base by Identifying the Catalytic Roles of Hydroxyl-Water-Cation Adducts</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2019-02-20</date><risdate>2019</risdate><volume>141</volume><issue>7</issue><spage>3232</spage><epage>3239</epage><pages>3232-3239</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><abstract>Despite the fundamental and practical significance of the hydrogen evolution and oxidation reactions (HER/HOR), their kinetics in base remain unclear. Herein, we show that the alkaline HER/HOR kinetics can be unified by the catalytic roles of the adsorbed hydroxyl (OHad)-water-alkali metal cation (AM+) adducts, on the basis of the observations that enriching the OHad abundance via surface Ni benefits the HER/HOR; increasing the AM+ concentration only promotes the HER, while varying the identity of AM+ affects both HER/HOR. The presence of OHad-(H2O) x -AM+ in the double-layer region facilitates the OHad removal into the bulk, forming OH–-(H2O) x -AM+ as per the hard–soft acid–base theory, thereby selectively promoting the HER. It can be detrimental to the HOR as per the bifunctional mechanism, as the AM+ destabilizes the OHad, which is further supported by the CO oxidation results. This new notion may be important for alkaline electrochemistry.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>30673227</pmid><doi>10.1021/jacs.8b13228</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1793-0741</orcidid><orcidid>https://orcid.org/0000-0002-6491-5504</orcidid><orcidid>https://orcid.org/0000-0003-1699-3089</orcidid><orcidid>https://orcid.org/0000-0003-1135-6742</orcidid><orcidid>https://orcid.org/0000-0001-9237-7603</orcidid><orcidid>https://orcid.org/0000-0002-2980-7655</orcidid><orcidid>https://orcid.org/0000-0002-4005-8894</orcidid><orcidid>https://orcid.org/0000000229807655</orcidid><orcidid>https://orcid.org/0000000317930741</orcidid><orcidid>https://orcid.org/0000000316993089</orcidid><orcidid>https://orcid.org/0000000240058894</orcidid><orcidid>https://orcid.org/0000000311356742</orcidid><orcidid>https://orcid.org/0000000264915504</orcidid><orcidid>https://orcid.org/0000000192377603</orcidid></addata></record> |
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title | Unifying the Hydrogen Evolution and Oxidation Reactions Kinetics in Base by Identifying the Catalytic Roles of Hydroxyl-Water-Cation Adducts |
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