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	<title>Publications &#8211; Energy Materials</title>
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	<title>Publications &#8211; Energy Materials</title>
	<link>https://www.presser-group.com</link>
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		<title>New paper published on pH-tolerant nickel-vanadium phosphonate framework supercapacitors in ACS Nano</title>
		<link>https://www.presser-group.com/new-paper-published-on-ph-tolerant-nickel-vanadium-phosphonate-framework-supercapacitors-in-acs-nano</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Mon, 06 Jul 2026 07:00:05 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=4007</guid>

					<description><![CDATA[New collaborative paper (lead: Gündoğ Yücesan) published in ACS Nano. We have developed a new nickel–vanadium phosphonate framework that combines redox-active metal centers with a chemically robust layered structure for aqueous energy storage. The material remains stable from pH 2 to 10, delivers up to about 300 F/g under slow-scan conditions, and retains its performance [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>New collaborative paper (lead: <a href="https://www.linkedin.com/in/dr-g%C3%BCndo%C4%9F-y%C3%BCcesan-bb90a4155/">Gündoğ Yücesan</a>) published in ACS Nano. We have developed a new nickel–vanadium phosphonate framework that combines redox-active metal centers with a chemically robust layered structure for aqueous energy storage. The material remains stable from pH 2 to 10, delivers up to about 300 F/g under slow-scan conditions, and retains its performance over more than 10,000 charge-discharge cycles in neutral and acidic electrolytes. Its sustainable water-based synthesis, broad pH tolerance, and exceptional cycling stability make it a promising platform for next-generation aqueous supercapacitors.</p>
<p><img fetchpriority="high" decoding="async" class="aligncenter size-full wp-image-4008" src="https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-23-124407.png" alt="" width="796" height="328" srcset="https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-23-124407.png 796w, https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-23-124407-705x291.png 705w, https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-23-124407-300x124.png 300w, https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-23-124407-768x316.png 768w" sizes="(max-width: 796px) 100vw, 796px" /></p>
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		<title>New collaborative paper published in Macromolecular Rapid Communications on hierarchically porous coatings for cellulose fibers</title>
		<link>https://www.presser-group.com/new-collaborative-paper-published-in-macromolecular-rapid-communications-on-hierarchically-porous-coatings-for-cellulose-fibers</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Fri, 03 Jul 2026 07:00:08 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3992</guid>

					<description><![CDATA[New collaborative paper published in Macromolecular Rapid Communications. In this study, we demonstrate a particle-templating strategy to create hierarchically porous, chemically functional coatings on cellulose fibers. Silica-polymer core-shell particles are deposited on cellulose paper and subsequently etched to generate porous polymer coatings with tunable surface chemistry, including hydroxy and epoxy groups. This approach opens new [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>New collaborative paper published in <a href="https://onlinelibrary.wiley.com/doi/10.1002/marc.70293">Macromolecular Rapid Communications</a>. In this study, we demonstrate a particle-templating strategy to create hierarchically porous, chemically functional coatings on cellulose fibers. Silica-polymer core-shell particles are deposited on cellulose paper and subsequently etched to generate porous polymer coatings with tunable surface chemistry, including hydroxy and epoxy groups. This approach opens new opportunities for smart cellulose-based filtration systems, paper-based sensors, and functional adsorbers.</p>
<p><img decoding="async" class="aligncenter size-full wp-image-3994" src="https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-04-131006.png" alt="" width="797" height="401" srcset="https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-04-131006.png 797w, https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-04-131006-705x355.png 705w, https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-04-131006-300x151.png 300w, https://www.presser-group.com/wp-content/uploads/2026/07/Screenshot-2026-07-04-131006-768x386.png 768w" sizes="(max-width: 797px) 100vw, 797px" /></p>
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		<title>New paper published in Water Research on terminology and metrics for electrosorption of trace organic compounds</title>
		<link>https://www.presser-group.com/new-paper-published-in-water-research-on-terminology-and-metrics-for-electrosorption-of-trace-organic-compounds</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Sat, 30 May 2026 09:13:23 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3948</guid>

					<description><![CDATA[New paper published in Water Research in collaboration with Helmholtz Centre for Environmental Research (Navid Saeidi &#38; Anett Georgi). Electrosorption is an emerging approach for removing and concentrating trace organic contaminants from water, including PFAS and pharmaceuticals, by combining conductive adsorbents with electrical control. This Making Waves article argues that such systems should not simply [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>New paper published in <a href="https://www.sciencedirect.com/science/article/pii/S0043135426008444">Water Research</a> in collaboration with Helmholtz Centre for Environmental Research (<a href="https://www.linkedin.com/in/navid-saeidi-b0631766/">Navid Saeidi</a> &amp; <a href="https://www.linkedin.com/in/anett-georgi-17280510/">Anett Georgi</a>). Electrosorption is an emerging approach for removing and concentrating trace organic contaminants from water, including PFAS and pharmaceuticals, by combining conductive adsorbents with electrical control. This Making Waves article argues that such systems should not simply borrow terminology and performance metrics from capacitive deionization, because trace-organic removal is often governed by adsorption affinity, selectivity, pore accessibility, and controlled release rather than charge-storage capacity. We propose a clearer terminology and reporting framework centered on metrics such as adsorption coefficients, breakthrough behavior, recovery, and enrichment to support better comparison between studies and accelerate the rational design of electrosorption technologies for water treatment.</p>
<p><img decoding="async" class="aligncenter size-large wp-image-3949" src="https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-30-111132-1030x424.png" alt="" width="1030" height="424" srcset="https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-30-111132-1030x424.png 1030w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-30-111132-705x290.png 705w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-30-111132-300x123.png 300w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-30-111132-768x316.png 768w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-30-111132.png 1269w" sizes="(max-width: 1030px) 100vw, 1030px" /></p>
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		<title>New paper published on nitrate reduction in Advanced Functional Materials</title>
		<link>https://www.presser-group.com/new-paper-published</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Mon, 18 May 2026 08:00:41 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3938</guid>

					<description><![CDATA[In a new collaborative paper in Advanced Functional Materials, we report an exfoliation-induced electrochemical reconstruction strategy that transforms CuCoAl layered double hydroxides into an amorphous/crystalline heterostructure for efficient nitrate reduction to ammonia. The reconstructed catalyst combines metallic Cu, crystalline Co(OH)2, and amorphous CoOOH, enabling high ammonia selectivity, excellent Faradaic efficiency, and strong cycling stability. Beyond [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>In a new collaborative paper in <a href="https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.75074">Advanced Functional Materials</a>, we report an exfoliation-induced electrochemical reconstruction strategy that transforms CuCoAl layered double hydroxides into an amorphous/crystalline heterostructure for efficient nitrate reduction to ammonia. The reconstructed catalyst combines metallic Cu, crystalline Co(OH)<sub>2</sub>, and amorphous CoOOH, enabling high ammonia selectivity, excellent Faradaic efficiency, and strong cycling stability. Beyond catalyst design, the study also demonstrates a Zn-NO<sub>2</sub><sup>&#8211;</sup> battery concept that links nitrate removal, ammonia production, and energy storage in one system.</p>
<p><img loading="lazy" decoding="async" class="aligncenter size-large wp-image-3943" src="https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-23-100923-1030x588.png" alt="" width="1030" height="588" srcset="https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-23-100923-1030x588.png 1030w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-23-100923-705x403.png 705w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-23-100923-300x171.png 300w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-23-100923-768x439.png 768w, https://www.presser-group.com/wp-content/uploads/2026/05/Screenshot-2026-05-23-100923.png 1187w" sizes="auto, (max-width: 1030px) 100vw, 1030px" /></p>
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		<title>New paper published in Energy Advances on lithium-ion extraction with lithium manganese oxide</title>
		<link>https://www.presser-group.com/new-paper-published-in-energy-advances-on-lithium-ion-extraction-with-lithium-manganese-oxide</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Mon, 27 Apr 2026 07:00:21 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3958</guid>

					<description><![CDATA[New collaborative work with University of Granada (Silvia Ahualli) published in RSC Energy Advances. This study explores an electrochemical route for selective lithium recovery from saline water using lithium manganese oxide, whose spinel structure can reversibly intercalate lithium ions under controlled cell voltages. By combining lithium manganese oxide with polyelectrolyte coatings, the work links ion [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>New collaborative work with <a href="https://www.ugr.es/">University of Granada</a> (<a href="https://fisicaaplicada.ugr.es/en/about/staff-directory/silvia-alejandra-ahualli-yapur/curriculum-vitae">Silvia Ahualli</a>) published in RSC <a href="https://pubs.rsc.org/en/content/articlelanding/2026/ya/d6ya00009f">Energy Advances</a>. This study explores an electrochemical route for selective lithium recovery from saline water using lithium manganese oxide, whose spinel structure can reversibly intercalate lithium ions under controlled cell voltages. By combining lithium manganese oxide with polyelectrolyte coatings, the work links ion selectivity, release dynamics, and electrode durability in both LiCl and mixed LiCl/NaCl solutions. Lithium uptake increased strongly with applied voltage, reaching values above 40 mg/g at 1.2 V, while the soft-electrode design maintained lithium selectivity even under challenging sodium-rich conditions.</p>
<p><img loading="lazy" decoding="async" class="aligncenter size-full wp-image-3961" src="https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-125719.png" alt="" width="967" height="343" srcset="https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-125719.png 967w, https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-125719-705x250.png 705w, https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-125719-300x106.png 300w, https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-125719-768x272.png 768w" sizes="auto, (max-width: 967px) 100vw, 967px" /></p>
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		<title>New paper published on Li-ion extraction from battery shredder solutions for recycling in ChemSusChem</title>
		<link>https://www.presser-group.com/new-paper-published-on-li-ion-extraction-from-battery-shredder-solutions-for-recycling-in-chemsuschem</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Mon, 27 Apr 2026 06:18:51 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3891</guid>

					<description><![CDATA[New paper published on electrochemical Li-ion extraction in the context of lithium-ion battery recycling in ChemSusChem. In this collaborative work with Fachhochschule Münster, we demonstrate an electrochemical route to recover lithium ions directly from real battery recycling process water generated during the wet shredding of lithium iron phosphate batteries. Using an LFP-based selective desalination cell, [&#8230;]]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph">New paper published on electrochemical Li-ion extraction in the context of lithium-ion battery recycling in <a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cssc.202502663">ChemSusChem</a>. In this collaborative work with Fachhochschule Münster, we demonstrate an electrochemical route to recover lithium ions directly from real battery recycling process water generated during the wet shredding of lithium iron phosphate batteries. Using an LFP-based selective desalination cell, the process produced a lithium-rich recovery solution with 96% purity, an average lithium uptake of 41 mg/g, and a low energy demand of only 1.10 kWh/kg. This study highlights electrochemical lithium recovery as a promising, lower-energy, and less chemically intensive pathway toward more circular battery recycling.</p>



<figure class="wp-block-image size-full"><img loading="lazy" decoding="async" width="1008" height="471" src="https://www.presser-group.com/wp-content/uploads/2026/04/image-1.png" alt="" class="wp-image-3893" srcset="https://www.presser-group.com/wp-content/uploads/2026/04/image-1.png 1008w, https://www.presser-group.com/wp-content/uploads/2026/04/image-1-705x329.png 705w, https://www.presser-group.com/wp-content/uploads/2026/04/image-1-300x140.png 300w, https://www.presser-group.com/wp-content/uploads/2026/04/image-1-768x359.png 768w" sizes="auto, (max-width: 1008px) 100vw, 1008px" /></figure>
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		<title>New paper published and featured on the front cover in Energy Advances on modified nanoporous carbons for lithium-sulfur batteries</title>
		<link>https://www.presser-group.com/new-paper-published-and-featured-on-the-front-cover-in-energy-advances-on-modified-nanoporous-carbons-for-lithium-sulfur-batteries</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Mon, 30 Mar 2026 07:00:49 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3966</guid>

					<description><![CDATA[New collaborative paper published in RSC Energy Advances. This study addresses one of the central challenges of lithium-sulfur batteries: capacity fading caused by polysulfide migration and incomplete confinement in carbon hosts. The team engineered a microporous carbon with a pore size of about 1.2 nm to host both short- and long-chain polysulfides, then further tuned [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>New collaborative paper published in RSC <a href="https://pubs.rsc.org/en/Content/ArticleLanding/2026/YA/D6YA00026F">Energy Advances</a>. This study addresses one of the central challenges of lithium-sulfur batteries: capacity fading caused by polysulfide migration and incomplete confinement in carbon hosts. The team engineered a microporous carbon with a pore size of about 1.2 nm to host both short- and long-chain polysulfides, then further tuned the carbon structure through urea and nickel sulfate treatments. The nickel sulfate-treated carbon-sulfur cathode showed improved cycling stability, reaching 72% capacity retention at C/20 and 96% retention at C/10 after 100 cycles, demonstrating a practical route to more stable Li-S battery cathodes. Our work was featured on the front cover</p>
<p><img loading="lazy" decoding="async" class="aligncenter size-full wp-image-3968" src="https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-194737.png" alt="" width="813" height="348" srcset="https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-194737.png 813w, https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-194737-705x302.png 705w, https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-194737-300x128.png 300w, https://www.presser-group.com/wp-content/uploads/2026/06/Screenshot-2026-06-19-194737-768x329.png 768w" sizes="auto, (max-width: 813px) 100vw, 813px" /> <img loading="lazy" decoding="async" class="aligncenter size-full wp-image-3967" src="https://www.presser-group.com/wp-content/uploads/2026/06/d6ya90010k.png" alt="" width="9922" height="12993" /></p>
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		<title>New paper published in EES Batteries on the electrochemical modeling of silicon in lithium-ion batteries</title>
		<link>https://www.presser-group.com/new-paper-published-in-ees-batteries-on-the-electrochemical-modeling-of-silicon-in-lithium-ion-batteries</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Thu, 26 Mar 2026 07:00:18 +0000</pubDate>
				<category><![CDATA[Group activities]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3952</guid>

					<description><![CDATA[New paper published in EES Batteries on the electrochemical modeling of silicon in lithium-ion batteries. In cooperation with industry partners and modelling experts, we presents a new electrochemical modeling framework for silicon anodes in lithium-ion batteries, capturing key challenges such as voltage hysteresis, phase transformations, and long relaxation processes. By combining multi-species, multi-reaction modeling with [&#8230;]]]></description>
										<content:encoded><![CDATA[<p>New paper published in <a href="https://pubs.rsc.org/en/content/articlelanding/2026/eb/d6eb00061d">EES Batteries</a> on the electrochemical modeling of silicon in lithium-ion batteries. In cooperation with industry partners and modelling experts, we presents a new electrochemical modeling framework for silicon anodes in lithium-ion batteries, capturing key challenges such as voltage hysteresis, phase transformations, and long relaxation processes. By combining multi-species, multi-reaction modeling with atomistic insights into lithium-silicon phases, the work provides a more realistic basis for understanding silicon electrodes and improving future battery design and management.</p>
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		<title>New paper published in Battery Energy on intraparticle effects on lithium-sulfur battery performance</title>
		<link>https://www.presser-group.com/new-paper-published-in-battery-energy-on-intraparticle-effects-on-lithium-sulfur-battery-performance</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Wed, 25 Mar 2026 06:23:47 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3861</guid>

					<description><![CDATA[New collaborative paper published in Battery Energy on &#8220;Intraparticular inhomogeneity limits capacity in lithium sulfur batteries with carbonate electrolyte&#8221;. This work shows that the performance of lithium-sulfur batteries with carbonate electrolytes is strongly governed by how the cathode-electrolyte interphase (CEI) forms inside nanoporous carbon host particles during the first discharge. Using cryogenic electron microscopy together [&#8230;]]]></description>
										<content:encoded><![CDATA[
<p class="wp-block-paragraph">New collaborative paper published in <a href="https://onlinelibrary.wiley.com/doi/10.1002/bte2.70111">Battery Energy</a> on &#8220;Intraparticular inhomogeneity limits capacity in lithium sulfur batteries with carbonate electrolyte&#8221;. This work shows that the performance of lithium-sulfur batteries with carbonate electrolytes is strongly governed by how the cathode-electrolyte interphase (CEI) forms inside nanoporous carbon host particles during the first discharge. Using cryogenic electron microscopy together with electrochemical analysis, we found that the CEI is not a uniform surface film but develops heterogeneously into the particle, leaving larger particles with inactive interior regions and therefore lower sulfur utilization. The results show that reducing carbon particle size improves capacity and rate performance, while also providing clear design guidelines for more efficient solid-state Li-S cathodes. Collaborative work with the groups of <a href="https://www.prehal-lab.eu/">Christian Prehal</a> and <a href="https://www.ki.si/en/about-the-institute/find-employees/315/">Alen Vizintin</a>.</p>



<figure class="wp-block-image size-full"><img loading="lazy" decoding="async" width="1018" height="485" src="https://www.presser-group.com/wp-content/uploads/2026/03/image-2.png" alt="" class="wp-image-3863" srcset="https://www.presser-group.com/wp-content/uploads/2026/03/image-2.png 1018w, https://www.presser-group.com/wp-content/uploads/2026/03/image-2-705x336.png 705w, https://www.presser-group.com/wp-content/uploads/2026/03/image-2-300x143.png 300w, https://www.presser-group.com/wp-content/uploads/2026/03/image-2-768x366.png 768w" sizes="auto, (max-width: 1018px) 100vw, 1018px" /></figure>
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		<title>New paper published in Battery Energy on mixed transition metal oxalates for lithium-ion batteries</title>
		<link>https://www.presser-group.com/new-paper-published-in-battery-energy-on-mixed-transition-metal-oxalates-for-lithium-ion-batteries</link>
		
		<dc:creator><![CDATA[vpresser]]></dc:creator>
		<pubDate>Mon, 23 Mar 2026 07:00:00 +0000</pubDate>
				<category><![CDATA[News]]></category>
		<category><![CDATA[Publications]]></category>
		<guid isPermaLink="false">https://www.presser-group.com/?p=3855</guid>

					<description><![CDATA[In our work, we have developed a new multi-phase transition metal oxalate anode material for lithium-ion batteries by combining five transition metals in a simple co-precipitation process, creating a structure that improves both charge transport and structural stability during cycling. The best-performing composition, TMOx-2, showed strong long-term performance, retaining 827 mAh/g after 400 cycles at [&#8230;]]]></description>
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<p class="wp-block-paragraph">In our work, we have developed a new multi-phase transition metal oxalate anode material for lithium-ion batteries by combining five transition metals in a simple co-precipitation process, creating a structure that improves both charge transport and structural stability during cycling. The best-performing composition, TMOx-2, showed strong long-term performance, retaining 827 mAh/g after 400 cycles at 100 mA/g and 498 mAh/g after 400 cycles at 500 mA/g. The study highlights how multi-phase design can enhance lithium storage performance without relying on complex synthesis routes, offering a promising strategy for next-generation high-performance battery materials.</p>



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