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Are metal-halide perovskite solar cells really radiation tolerant?
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2025.101852
Ahmad R. Kirmani , Ian R. Sellers
{"title":"Are metal-halide perovskite solar cells really radiation tolerant?","authors":"Ahmad R. Kirmani ,&nbsp;Ian R. Sellers","doi":"10.1016/j.joule.2025.101852","DOIUrl":"10.1016/j.joule.2025.101852","url":null,"abstract":"<div><div>Recent evidence of radiation tolerance and self-healing in metal-halide perovskites has spurred interest in their potential as a scalable and low-cost space power technology for the emerging commercial space economy. In this perspective, we challenge the prevailing narrative around this radiation tolerance, suggesting that perovskites may not be as tolerant as currently perceived and that further work is needed to fully understand radiation-matter interactions in these systems. We suggest that a unique combination of lattice softness, strong electron-phonon coupling, and low intrinsic thermal conductivity places halide perovskites in a category of unconventional semiconductors, enabling them to self-heal from radiation-induced displacement damage, unexpected for structurally vulnerable materials. Nevertheless, we postulate that the tendency for halide perovskites to self-heal might also be their Achilles’ heel, making them vulnerable to ionizing radiation that involves sharp localized phonon-mediated temperature spikes and decomposition at higher radiation fluence. Calling attention to this unusual characteristic, we attempt to spur the development of theoretical and experimental insights with the goal of realizing tailored device architectures that can withstand coupled extremes where radiation, thermal cycling, vacuum, and air mass 0 (AM0) illumination join forces and inflict catastrophic nonlinear damage.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101852"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143518509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Photobatteries: Prospects and fundamental limitations
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2025.101869
Arvind Pujari , Kohei Shimokawa , Michael De Volder
{"title":"Photobatteries: Prospects and fundamental limitations","authors":"Arvind Pujari ,&nbsp;Kohei Shimokawa ,&nbsp;Michael De Volder","doi":"10.1016/j.joule.2025.101869","DOIUrl":"10.1016/j.joule.2025.101869","url":null,"abstract":"<div><div>The need for autonomous off-grid energy sources has led to the development of “photobatteries,” which combine the dual functionalities of light-energy harvesting and electrochemical energy storage within the same device architecture. Although several interesting devices and materials have been reported recently, there remains a wide disparity between proposed mechanisms and measurement methods between various publications. In this perspective, we highlight the current issues in the field and provide possible solutions and avenues for future developments. We focus on the requirements for autonomous photocharging to be possible and the need for standardized measurement protocols, especially in relation to decoupling thermal and optical effects. These protocols lay the framework for the stepwise fabrication of photobatteries—from photo-enhanced to fully photo-rechargeable systems. We also highlight prospective use cases of photobatteries; for example, there are substantial technological challenges that need to be addressed before grid-scale energy storage becomes viable, but in the short term, they might be attractive for small off-grid devices.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101869"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143582488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Carboxyl-functionalized perovskite enables ALD growth of a compact and uniform ion migration barrier 羧基官能化钙钛矿使ALD生长成致密均匀的离子迁移屏障
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2024.12.002
Deokjae Choi , Donghoon Shin , Chongwen Li , Yuan Liu , Abdulaziz S.R. Bati , Dana E. Kachman , Yi Yang , Jiachen Li , Yoon Jung Lee , Muzhi Li , Saivineeth Penukula , Da Bin Kim , Heejong Shin , Chiung-Han Chen , So Min Park , Cheng Liu , Aidan Maxwell , Haoyue Wan , Nicholas Rolston , Edward H. Sargent , Bin Chen
{"title":"Carboxyl-functionalized perovskite enables ALD growth of a compact and uniform ion migration barrier","authors":"Deokjae Choi ,&nbsp;Donghoon Shin ,&nbsp;Chongwen Li ,&nbsp;Yuan Liu ,&nbsp;Abdulaziz S.R. Bati ,&nbsp;Dana E. Kachman ,&nbsp;Yi Yang ,&nbsp;Jiachen Li ,&nbsp;Yoon Jung Lee ,&nbsp;Muzhi Li ,&nbsp;Saivineeth Penukula ,&nbsp;Da Bin Kim ,&nbsp;Heejong Shin ,&nbsp;Chiung-Han Chen ,&nbsp;So Min Park ,&nbsp;Cheng Liu ,&nbsp;Aidan Maxwell ,&nbsp;Haoyue Wan ,&nbsp;Nicholas Rolston ,&nbsp;Edward H. Sargent ,&nbsp;Bin Chen","doi":"10.1016/j.joule.2024.12.002","DOIUrl":"10.1016/j.joule.2024.12.002","url":null,"abstract":"<div><div>Mixed-halide wide-band-gap perovskites are critical components of highly efficient tandem cells, but their operating stability is limited by halide migration. Metal oxides deposited via atomic layer deposition (ALD) have been shown to block halide migration; however, previously pursued methods result in inhomogeneous nucleation and growth. We hypothesized that functionalizing the perovskite surface with ALD-active carboxyl groups could promote nucleation and enable higher-temperature metal oxide growth. We find that 5-ammonium valeric acid iodide (5-AVAI) facilitates the formation of a compact and uniform aluminum oxide (Al<sub>2</sub>O<sub>3</sub>) layer and allows growth at 100°C compared with the previous limit of 75°C. We demonstrate that halide migration into the C<sub>60</sub> electron transport layer is reduced by a factor of 10 compared with the reference case. Al<sub>2</sub>O<sub>3</sub>-capped perovskite solar cells with a band gap of 1.78 eV retain 90% of their initial power conversion efficiency after 1,000 h of continuous operation under 1-sun illumination at 55°C.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101801"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142937597","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In situ electrochemical regeneration of permanganate ion for sustainable oxidation reactions 高锰酸盐离子持续氧化反应的原位电化学再生
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2024.101807
Chengyi Hu , Zixiao Zhao , Wanli Wang , Weijie Zou , Shengjun Liu , Xiaoliang Fang , Xiangyu Su , Nanfeng Zheng
{"title":"In situ electrochemical regeneration of permanganate ion for sustainable oxidation reactions","authors":"Chengyi Hu ,&nbsp;Zixiao Zhao ,&nbsp;Wanli Wang ,&nbsp;Weijie Zou ,&nbsp;Shengjun Liu ,&nbsp;Xiaoliang Fang ,&nbsp;Xiangyu Su ,&nbsp;Nanfeng Zheng","doi":"10.1016/j.joule.2024.101807","DOIUrl":"10.1016/j.joule.2024.101807","url":null,"abstract":"<div><div>Numerous stoichiometric oxidants have been employed for the oxidative production of high-end fine chemicals. However, regeneration of these oxidants often suffers from high energy consumption and complex separation. Here, we report an <em>in situ</em> electrochemical approach for the regeneration of a widely used oxidant, permanganate (MnO<sub>4</sub><sup>−</sup>), by coupling electrochemical and chemical reactions in an integrated system. Using electrosynthesis of 1,3,2-dioxathiolane 2,2-dioxide (DTD), a commercial electrolyte additive in Li-ion batteries, as a representative example, the electrochemically generated MnO<sub>4</sub><sup>−</sup> shows remarkable performance as a redox mediator for catalyzing ethylene sulfite oxidation to produce DTD. By employing pulsed voltammetry, electrosynthesis of DTD can be performed in a single-pass continuous flow electrolyzer with 85% yield and 72% Faradaic efficiency. The practicality of the developed method is demonstrated with a wide substrate scope, robust anode stability, and scaling capability to achieve a DTD production capacity of 500 g/h in a 1-m<sup>2</sup> electrolyzer.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101807"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142991173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Temperature-dependent solid electrolyte interphase reactions drive performance in lithium-mediated nitrogen reduction to ammonia 温度依赖的固体电解质相间反应驱动锂介导的氮还原成氨的性能
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2024.101810
Peter Benedek , Yamile E. Cornejo-Carrillo , Alden H. O’Rafferty , Valerie A. Niemann , Sang-Won Lee , Eric J. McShane , Matteo Cargnello , Adam C. Nielander , Thomas F. Jaramillo
{"title":"Temperature-dependent solid electrolyte interphase reactions drive performance in lithium-mediated nitrogen reduction to ammonia","authors":"Peter Benedek ,&nbsp;Yamile E. Cornejo-Carrillo ,&nbsp;Alden H. O’Rafferty ,&nbsp;Valerie A. Niemann ,&nbsp;Sang-Won Lee ,&nbsp;Eric J. McShane ,&nbsp;Matteo Cargnello ,&nbsp;Adam C. Nielander ,&nbsp;Thomas F. Jaramillo","doi":"10.1016/j.joule.2024.101810","DOIUrl":"10.1016/j.joule.2024.101810","url":null,"abstract":"<div><div>The solid electrolyte interphase (SEI) is a vital component to control mass transport and selectivity in the lithium-mediated reduction of N<sub>2</sub> to NH<sub>3</sub> (Li-N<sub>2</sub>R). Finding strategies that generate the optimal SEI, a complex network of organic and inorganic species, can potentially improve Li-N<sub>2</sub>R performance. Here, we unravel structure-property relationships of the SEI by correlating its composition with the NH<sub>3</sub> Faradaic efficiency (FE<sub>NH3</sub>). By modifying the reaction temperature, we alter electrolyte decomposition reactions and observe changes in the SEI that explain FE<sub>NH3</sub> trends between electrolyte solvents. We quantify a complex reaction environment at elevated temperatures where SEI formation is counteracted by etching reactions. This trade-off leads to temporal fluctuations of FE<sub>NH3</sub>, but the maximal FE<sub>NH3</sub> can reach up to 40%, the highest value reported for batch cells at ambient pressure thus far. Our work underscores the potential of novel electrolytes that steer SEI selectivity and, ultimately, improve Li-N<sub>2</sub>R performance.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101810"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143020864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hybrid solvating electrolytes for practical sodium-metal batteries
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2024.101811
Weiyin Chen , Jin-Sung Park , Choah Kwon , Christian O. Plaza-Rivera , Chia-Wei Hsu , Jason Khoi Phong , Landon James Kilgallon , Daniel Wang , Tao Dai , So Yeon Kim , Guanzhou Zhu , Yifan Gao , Zhichu Ren , Zhen Zhang , Hyojun Lim , Yang Shao-Horn , Jeremiah A. Johnson , Ju Li
{"title":"Hybrid solvating electrolytes for practical sodium-metal batteries","authors":"Weiyin Chen ,&nbsp;Jin-Sung Park ,&nbsp;Choah Kwon ,&nbsp;Christian O. Plaza-Rivera ,&nbsp;Chia-Wei Hsu ,&nbsp;Jason Khoi Phong ,&nbsp;Landon James Kilgallon ,&nbsp;Daniel Wang ,&nbsp;Tao Dai ,&nbsp;So Yeon Kim ,&nbsp;Guanzhou Zhu ,&nbsp;Yifan Gao ,&nbsp;Zhichu Ren ,&nbsp;Zhen Zhang ,&nbsp;Hyojun Lim ,&nbsp;Yang Shao-Horn ,&nbsp;Jeremiah A. Johnson ,&nbsp;Ju Li","doi":"10.1016/j.joule.2024.101811","DOIUrl":"10.1016/j.joule.2024.101811","url":null,"abstract":"<div><div>Sodium-metal batteries could be competitive against Li-metal batteries, but their applications depend on the stability of electrolytes against sodium-metal anodes and cathodes simultaneously. Here, we propose hybrid solvating electrolytes (HSEs), composed of both strongly and weakly solvating solvents of sodium salts, to tune the solubility, solvation structure, and electrochemical decomposition properties. Fifty HSEs are prepared using the pre-screened candidate molecules, validating the mixture selection requirements and correlations between salt/solvent types and their mixture-dependent performance, including oxidative stability, Coulombic efficiency, and cycling overpotential. A model hybrid solvent formed by mixing weakly solvating N,N-dimethyltrifluoromethane sulfonamide (DMTMSA) with strongly solvating tetrahydrofuran (THF) demonstrates strong beyond-rule-of-mixture effects, showing extraordinarily stable cycling performance against Na<sub>3</sub>V<sub>2</sub>(PO<sub>4</sub>)<sub>3</sub> and Na<sub>0.44</sub>MnO<sub>2</sub> cathodes and Na-metal anode. Spectroscopic analysis and molecular dynamics simulations reflect the corresponding change in ion-dipole interaction and solvation structures. The strong-weak hybrid solvating principle for electrolyte design enables practical alkali-metal batteries.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101811"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143026956","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Simplified photocatalyst sheets unlock scalable water splitting
IF 38.6 1区 材料科学
Joule Pub Date : 2025-03-19 DOI: 10.1016/j.joule.2025.101882
Xiangjiu Guan , Shaohua Shen
{"title":"Simplified photocatalyst sheets unlock scalable water splitting","authors":"Xiangjiu Guan ,&nbsp;Shaohua Shen","doi":"10.1016/j.joule.2025.101882","DOIUrl":"10.1016/j.joule.2025.101882","url":null,"abstract":"<div><div>As reported recently in <em>Chem Catalysis</em>, Domen and coworkers developed a facile filtration method for preparing photocatalyst sheets, achieving a solar-to-hydrogen energy conversion efficiency of 0.4% while also being capable of operating at atmospheric pressure, which opens a new way of fabricating efficient photocatalyst sheets for commercial-scale solar hydrogen production.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 3","pages":"Article 101882"},"PeriodicalIF":38.6,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143642139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enabling 6C fast charging of Li-ion batteries at sub-zero temperatures via interface engineering and 3D architectures
IF 39.8 1区 材料科学
Joule Pub Date : 2025-03-17 DOI: 10.1016/j.joule.2025.101881
Tae H. Cho, Yuxin Chen, Daniel W. Liao, Eric Kazyak, Daniel Penley, Manoj K. Jangid, Neil P. Dasgupta
{"title":"Enabling 6C fast charging of Li-ion batteries at sub-zero temperatures via interface engineering and 3D architectures","authors":"Tae H. Cho, Yuxin Chen, Daniel W. Liao, Eric Kazyak, Daniel Penley, Manoj K. Jangid, Neil P. Dasgupta","doi":"10.1016/j.joule.2025.101881","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101881","url":null,"abstract":"Addressing the trilemma between fast-charging, low-temperature operation, and high-energy-density electrodes is critical to advance Li-ion batteries. Here, we introduce a strategy that integrates 3D electrode architectures with an artificial solid-electrolyte interface (SEI) using atomic layer deposition of a solid electrolyte (Li<sub>3</sub>BO<sub>3</sub>-Li<sub>2</sub>CO<sub>3</sub>). These synergistic modifications enhance both mass transport and interfacial kinetics under low temperatures and fast charging, increasing the accessible capacity of thick electrodes (&gt;3 mAh/cm<sup>2</sup>). To decouple the contributions from electrolyte transport and interfacial impedance, graphite/Li<sub>x</sub>Ni<sub>y</sub>Mn<sub>z</sub>Co<sub>a</sub>O (NMC) pouch cells were fabricated and their electrochemical performances were tested under low-temperature, fast-charging conditions. At a 6C-rate and a temperature of −10°C, these integrated electrodes enabled a &gt;500% increase in accessible capacity and &gt;97% capacity retention after 100 cycles, without Li plating. The capacity retention under low-temperature, fast-charging conditions was also dependent on the state-of-charge swing, highlighting the importance of the charging protocol to minimize Li plating.","PeriodicalId":343,"journal":{"name":"Joule","volume":"33 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143635647","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Susceptible organic cations enable stable and efficient perovskite solar cells
IF 39.8 1区 材料科学
Joule Pub Date : 2025-03-17 DOI: 10.1016/j.joule.2025.101879
Jongbeom Kim, Jaewang Park, Jihoo Lim, Jaehui Kim, Junseok Kim, Nahye Shin, Jae Sung Yun, Jino Im, Sang Il Seok
{"title":"Susceptible organic cations enable stable and efficient perovskite solar cells","authors":"Jongbeom Kim, Jaewang Park, Jihoo Lim, Jaehui Kim, Junseok Kim, Nahye Shin, Jae Sung Yun, Jino Im, Sang Il Seok","doi":"10.1016/j.joule.2025.101879","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101879","url":null,"abstract":"Achieving higher open-circuit voltages and fill factors in perovskite solar cells (PSCs) involves minimizing defects between layers and maximizing carrier extraction and transport. One approach includes integrating a two-dimensional (2D) semiconducting interlayer to form a heterojunction with the perovskite absorber. However, conventional 2D layers often have poor thermal stability due to the migration of organic cations. This study examines the enhancement in power conversion efficiency (PCE) and thermal stability of PSCs by using strong intermolecular interactions between methoxy-phenethylammonium iodide and cyclohexylammonium bromide as chosen organic cations. The resulting 2D/perovskite configuration facilitates efficient charge transfer and demonstrates superior thermal stability at 85°C. The optimized PSCs achieved a PCE of 26.28% under air mass (AM) 1.5G illumination, retaining 88% efficiency after 440 h of continuous illumination and maintaining 100% of its initial efficiency after 9,000 h under ambient conditions. This research contributes to developing highly efficient and stable PSCs.","PeriodicalId":343,"journal":{"name":"Joule","volume":"89 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143635646","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Process cost analysis of performance challenges and their mitigations in sodium-ion battery cathode materials
IF 39.8 1区 材料科学
Joule Pub Date : 2025-03-14 DOI: 10.1016/j.joule.2025.101871
Mrigi Munjal, Thorben Prein, Mahmoud M. Ramadan, Hugh B. Smith, Vineeth Venugopal, Jennifer L.M. Rupp, Iwnetim I. Abate, Elsa A. Olivetti, Kevin J. Huang
{"title":"Process cost analysis of performance challenges and their mitigations in sodium-ion battery cathode materials","authors":"Mrigi Munjal, Thorben Prein, Mahmoud M. Ramadan, Hugh B. Smith, Vineeth Venugopal, Jennifer L.M. Rupp, Iwnetim I. Abate, Elsa A. Olivetti, Kevin J. Huang","doi":"10.1016/j.joule.2025.101871","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101871","url":null,"abstract":"The success of sodium-ion batteries (SIBs) hinges on mitigating underperformance in ways that are cost effective, manufacturable, and scalable. This work investigates interfacial, morphological, and bulk interventions to enhance the performance of layered metal oxide cathode active materials (CAMs) for SIBs. We mapped the full space of literature-reported SIB CAM challenges and their mitigations. We then estimated the manufacturing costs for a diverse and representative set of mitigation approaches. Adding sacrificial salts can be cost effective, given low materials costs and minimal process changes. By contrast, many methods are reported to tune CAM morphology. Several are likely challenging at scale due to process throughput and yield limitations. Finally, bulk modifications can mitigate the moisture sensitivity of some CAMs, a likely less costly route than expanding stringent atmosphere controls during manufacturing. We end by discussing the limits and promise of process cost analysis, given the current state of battery reporting in the literature.","PeriodicalId":343,"journal":{"name":"Joule","volume":"54 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143618885","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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