<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Das, Chandni</style></author><author><style face="normal" font="default" size="100%">Sinha, Nibedita</style></author><author><style face="normal" font="default" size="100%">Nair, Aathira</style></author><author><style face="normal" font="default" size="100%">Pal, Santanu</style></author><author><style face="normal" font="default" size="100%">Joshi, Kavita</style></author><author><style face="normal" font="default" size="100%">Roy, Poulomi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Chlorophobic iron hydrogen phosphite as OER-active electrocatalyst in anion exchange membrane (sea)water electrolysis</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AEM electrolyzer</style></keyword><keyword><style  face="normal" font="default" size="100%">chloride repellant</style></keyword><keyword><style  face="normal" font="default" size="100%">electrocatalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">hydrogen production</style></keyword><keyword><style  face="normal" font="default" size="100%">seawater oxidation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">AUG</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">21</style></volume><pages><style face="normal" font="default" size="100%">2505781</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Seawater electrolysis is recognized as a promising technology to cater to the worldwide drive for sustainable hydrogen production; however, its practical viability is often hindered by the inevitable anode corrosion arising from the electrode side reactions owing to the presence of high chloride content which eventually degrade the electrode performance eventually. Herein, the design of unprecedented ammonium iron hydrogen phosphite (FeHPhi) along with a trace amount of Cu, is reported as the unique and much desired electrode material for seawater electrolysis due to its special chloride repellant nature along with great electrocatalytic activity toward water oxidation. The [HPO3](2-) oxoanion as Lewis base in the structure effectively restricts chloride ions, while the Fe center acts as Lewis acid offering an active site for water oxidation, also well-supported theoretically. Leveraging this frustrated Lewis pair combination, the electrocatalyst achieves a high current density of 500 mA cm(-2) at 344 mV overpotential in alkaline real seawater with impressive robustness to sustain for 200 h when operated under chlorine evolution reaction dominating region (&amp;gt;2 V). The electrocatalyst also demonstrates superior performance in anion exchange membrane freshwater and seawater electrolysis, demonstrating its potential applicability.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">34</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;
	Foreign&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	12.1&lt;/p&gt;
</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sinha, Nibedita</style></author><author><style face="normal" font="default" size="100%">Das, Chandni</style></author><author><style face="normal" font="default" size="100%">Er, Chen-Chen</style></author><author><style face="normal" font="default" size="100%">Urkude, Rajashri R.</style></author><author><style face="normal" font="default" size="100%">Pal, Santanu</style></author><author><style face="normal" font="default" size="100%">Ghosh, Biplab</style></author><author><style face="normal" font="default" size="100%">Chai, Siang-Piao</style></author><author><style face="normal" font="default" size="100%">Roy, Poulomi</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Dynamic and resilient cobalt copper nitride and iron nitride heterostructure aided energy economic urea electrolysis in anion exchange membrane electrolyzer</style></title><secondary-title><style face="normal" font="default" size="100%">Small</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">AEM electrolyzer</style></keyword><keyword><style  face="normal" font="default" size="100%">heterostructured electrocatalyst</style></keyword><keyword><style  face="normal" font="default" size="100%">reversible adaptability</style></keyword><keyword><style  face="normal" font="default" size="100%">urea oxidation</style></keyword><keyword><style  face="normal" font="default" size="100%">Water oxidation</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2026</style></year><pub-dates><date><style  face="normal" font="default" size="100%">MAY</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">22</style></volume><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Urea oxidation reaction (UOR) is recognized for energy-efficient hydrogen production, which nonetheless requires a meticulously designed electrocatalyst with active sites for intermediates adsorption and gaseous products desorption to fully exploit its advantages. Herein, we design the heterostructure consisting of cobalt copper nitride and iron nitride (Co3CuN/FexNy) as an efficient and trifunctional electrocatalyst, which requires 1.35 VRHE, 1.55 VRHE, and 0.23 VRHE potentials to reach 100 mA cm-2 current density for UOR, oxygen evolution reaction (OER), and hydrogen evolution reaction (HER), respectively. Unlike the conventional UOR selective electrocatalyst, Co3CuN/FexNy not only facilitates the UOR -&amp;gt; OER switching but also shows self-regulatory ability in UOR &amp;lt;-&amp;gt; OER. The Density Functional Theory (DFT) study explained that while Co3CuN promoted the adsorption of CO(NH2)2 and H2O, FexNy facilitated CO2 and N2 desorption, resulting in accelerated UOR and HER kinetics. The electrocatalyst also demonstrated outstanding performance in a urea-coupled AEM electrolyzer with about 20% of power saving and great electrolyzer efficiency, further highlighting its potential for industry-relevant applications.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">30</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;
	Foreign&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	11.8&lt;/p&gt;
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