<?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%">Kumar, Hitesh</style></author><author><style face="normal" font="default" size="100%">Ottakam Thotiyl, Musthafa</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%">Activating lattice oxygen via proton-decoupled electron transfer in iron chromium phosphate for efficient (sea)water oxidation</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry A</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2026</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%">14</style></volume><pages><style face="normal" font="default" size="100%">32691-32705</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	Given the escalating freshwater scarcity crisis, seawater oxidation has emerged as a promising approach to advancing sustainable hydrogen production; however, its practical feasibility is severely hindered by pervasive chloride-induced corrosion. In this study, we develop an efficient FeCr-phosphate (FeCrPi) as an electrocatalyst by a simple solvothermal strategy, which exhibits superior oxygen evolution reaction (OER) activity in both alkaline freshwater and seawater. The rational design of FeCrPi affords dual advantages: phosphate groups promote the lattice oxygen mechanism (LOM), while the CrO42- species generated in situ during seawater oxidation adsorb onto the electrode surface, creating a protective layer that mitigates chloride corrosion, suppress the chlorine evolution reaction (CER), and enhance the OER selectivity. As a result, FeCrPi demonstrates excellent OER activity in alkaline freshwater and alkaline real seawater, achieving a high current density of 0.5 A cm-2 at 280 and 340 mV, respectively, and also maintaining an impressive stability over 100 h at a high applied potential of 2 V in real alkaline seawater. This work establishes a viable phosphate-engineering strategy for fabricating a highly efficient chloride-resistive electrocatalyst with OER selectivity, which enables LOM-assisted seawater oxidation.&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">48</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;
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	9.2&lt;/p&gt;
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