{"title":"Enriched asymmetric π electrons confining single-site Pt for acidic hydrogen evolution","authors":"Mingxia Xu, Yiran Kang, Leilei Wang, Yunlong Zhang, Guang Jiang, Yafeng Cai, Yunchuan Tu, Qiao Zhao, Jun Chi, Wei Song, Hongmei Yu, Jingting Hu, Wei Liu, Rui Huang, Liang Yu, Junling Lu, Xinhe Bao, Dehui Deng","doi":"10.1016/j.joule.2025.101968","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101968","url":null,"abstract":"Achieving both high activity and durability with minimal Pt loading is critical for acidic hydrogen evolution in large-scale proton exchange membrane water electrolyzers (PEMWEs), in which precise regulation of Pt-support interaction is the key yet remains a great challenge. Here, we report that by confining single-site Pt with enriched asymmetric π electrons on a monolayer graphene encapsulating CoNi nanoalloy, a highly active and durable Pt site is constructed, which delivers an unprecedented mass activity. Assembled PEMWE using this catalyst achieves a record-high current density of 4.0 A cm<sup>−2</sup> at 2.02 V with the lowest-ever-reported Pt loading of 1.2 μg<sub>Pt</sub> cm<sup>−2</sup> and exhibits an excellent durability of 1,000 h at 2 A cm<sup>−2</sup>. Comprehensive investigations reveal that CoNi-graphene 3<em>d</em>-2<em>p</em> orbital overlapping combined with CoNi-to-carbon electron transfer, perturbs the conjugation effect and orbital symmetry of graphene π electrons, leading to reinforced Pt–graphene bonding and electron enrichment on Pt, which enhances both catalytic stability and activity.","PeriodicalId":343,"journal":{"name":"Joule","volume":"2 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144153972","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}
JoulePub Date : 2025-05-22DOI: 10.1016/j.joule.2025.101965
Narumi Nagaya, Kangmin Lee, Collin F. Perkinson, Aaron Li, Youri Lee, Xinjue Zhong, Sujin Lee, Leah P. Weisburn, Janet Z. Wang, Tomi K. Baikie, Moungi G. Bawendi, Troy Van Voorhis, William A. Tisdale, Antoine Kahn, Kwanyong Seo, Marc A. Baldo
{"title":"Exciton fission enhanced silicon solar cell","authors":"Narumi Nagaya, Kangmin Lee, Collin F. Perkinson, Aaron Li, Youri Lee, Xinjue Zhong, Sujin Lee, Leah P. Weisburn, Janet Z. Wang, Tomi K. Baikie, Moungi G. Bawendi, Troy Van Voorhis, William A. Tisdale, Antoine Kahn, Kwanyong Seo, Marc A. Baldo","doi":"10.1016/j.joule.2025.101965","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101965","url":null,"abstract":"While silicon solar cells dominate global photovoltaic energy production, their continued improvement is hindered by the single-junction limit. One potential solution is to use molecular singlet exciton fission to generate two electrons from each absorbed high-energy photon. We demonstrate that the long-standing challenge of coupling molecular excited states to silicon solar cells can be overcome using sequential charge transfer. Combining zinc phthalocyanine, aluminum oxide, and a shallow junction crystalline silicon microwire solar cell, the peak charge generation efficiency per photon absorbed in tetracene is (138% ± 6%), comfortably surpassing the quantum efficiency limit for conventional silicon solar cells and establishing a new, scalable approach to low-cost, high-efficiency photovoltaics.","PeriodicalId":343,"journal":{"name":"Joule","volume":"20 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144114329","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}
JoulePub Date : 2025-05-21DOI: 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":"10.1016/j.joule.2025.101871","url":null,"abstract":"<div><div>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.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101871"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","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}
JoulePub Date : 2025-05-21DOI: 10.1016/j.joule.2025.101884
Jinwook Rhyu , Joachim Schaeffer , Michael L. Li , Xiao Cui , William C. Chueh , Martin Z. Bazant , Richard D. Braatz
{"title":"Systematic feature design for cycle life prediction of lithium-ion batteries during formation","authors":"Jinwook Rhyu , Joachim Schaeffer , Michael L. Li , Xiao Cui , William C. Chueh , Martin Z. Bazant , Richard D. Braatz","doi":"10.1016/j.joule.2025.101884","DOIUrl":"10.1016/j.joule.2025.101884","url":null,"abstract":"<div><div>Optimization of the formation step in lithium-ion battery manufacturing is challenging due to limited physical understanding of solid-electrolyte interphase formation and the long testing time (∼100 days) for cells to reach the end of life. We propose a systematic feature-design framework that requires minimal domain knowledge for accurate cycle life prediction during formation. By only using two simple <span><math><mrow><mi>Q</mi><mrow><mo>(</mo><mi>V</mi><mo>)</mo></mrow></mrow></math></span> features designed from our framework, extracted from formation data without any additional diagnostic cycles, we achieved an average of 9.87% error for cycle life prediction. The physics-based investigation guided by the two designed features shows that the voltage ranges identified by our framework capture the effects of formation temperature and microscopic-particle resistance heterogeneity. By designing highly predictive, robust, and interpretable features, our approach can accelerate industrial battery formation research, leveraging the interplay between data-driven feature design and mechanistic understanding.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101884"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143723841","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}
JoulePub Date : 2025-05-21DOI: 10.1016/j.joule.2025.101972
Sandy Sánchez-Alonso, Lukas Pfeifer, Ornella Vaccarelli, Christophe Gisler, Jean Hennebert, Felix T. Eickemeyer, Rafael Ferragut, Kevin Sivula, Michael Graetzel
{"title":"TEMPO bulk passivation boosts the performance and operational stability of rapid-annealed FAPI perovskite solar cells","authors":"Sandy Sánchez-Alonso, Lukas Pfeifer, Ornella Vaccarelli, Christophe Gisler, Jean Hennebert, Felix T. Eickemeyer, Rafael Ferragut, Kevin Sivula, Michael Graetzel","doi":"10.1016/j.joule.2025.101972","DOIUrl":"https://doi.org/10.1016/j.joule.2025.101972","url":null,"abstract":"In this work, we present a high-performance, stable formamidinium lead iodide (FAPI) perovskite solar cell (PSC) achieved through the use of 2,2,6,6-tetramethylpiperidinyloxyl (TEMPO) bulk passivation and rapid photonic annealing. Utilizing flash infrared annealing (FIRA), we fabricated TEMPO-FAPI PSCs with a power conversion efficiency (PCE) exceeding 20%, exceeding the prior state of the art for this process. The TEMPO additive promotes enhanced crystallization dynamics, yielding films with improved homogeneity and reduced defect densities, as confirmed by photoluminescence (PL), profilometry, and positron annihilation lifetime spectroscopy (PALS). Stability testing under ISOS protocols demonstrated that the TEMPO-FAPI devices retained over 90% of their initial PCE after 4,296 h of operational and thermal stress, showing unprecedented longevity for a rapid processing technique. TEMPO’s primary effect on passivating grain boundaries and surface defects is evidenced by a significantly reduced non-radiative recombination rate and low defect density, establishing this molecule as a promising additive for scalable, durable FAPI PSC manufacturing.","PeriodicalId":343,"journal":{"name":"Joule","volume":"2 1","pages":""},"PeriodicalIF":39.8,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144104008","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}
JoulePub Date : 2025-05-21DOI: 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":"10.1016/j.joule.2025.101881","url":null,"abstract":"<div><div>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 (>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 >500% increase in accessible capacity and >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.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101881"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","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}
JoulePub Date : 2025-05-21DOI: 10.1016/j.joule.2025.101888
Xiang Li , Yu Wei , Xiang Gao , Zhongqiang Zhang , Zhong Lin Wang , Di Wei
{"title":"Harnessing triboiontronic Maxwell’s demon by triboelectric-induced polarization for efficient energy-information flow","authors":"Xiang Li , Yu Wei , Xiang Gao , Zhongqiang Zhang , Zhong Lin Wang , Di Wei","doi":"10.1016/j.joule.2025.101888","DOIUrl":"10.1016/j.joule.2025.101888","url":null,"abstract":"<div><div>Maxwell’s demon seemingly violates the second law of thermodynamics, but in reality, it requires external energy for information processing and particle control, thereby ensuring an overall increase in system entropy. Here, triboiontronic Maxwell’s demon was established by triboelectric-induced polarization, enabling remote regulation of charge migration within electrical double layers (EDLs). For energy flow, an enhanced physical-adsorption triboiontronic nanogenerator (EP-TING) achieved a remarkable transferred charge density of 2,347.12 mC/m<sup>2</sup>, surpassing conventional EDL-based technologies by several orders of magnitude. Furthermore, the advanced synergy-enhanced strategy TING (ES-TING), integrating redox reactions, further increased the charge density to 5,237.51 mC/m<sup>2</sup>, marking a significant breakthrough in energy conversion efficiency. For information flow, bionic neural circuits utilizing EP-TINGs/ES-TINGs enabled highly portable, interference-resistant underwater transmission systems with minimal energy consumption, effectively addressing challenges of acoustic multipath interference, environmental noise, and severe signal attenuation. Therefore, harnessing triboiontronic Maxwell’s demon provides an efficient energy-information flow, proving crucial in the post-Moore era.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101888"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143737271","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}
JoulePub Date : 2025-05-21DOI: 10.1016/j.joule.2025.101960
Emmanuel Defay
{"title":"Elastocaloric goes compact","authors":"Emmanuel Defay","doi":"10.1016/j.joule.2025.101960","DOIUrl":"10.1016/j.joule.2025.101960","url":null,"abstract":"<div><div>In a recent issue of <em>Device</em>, Zhang et al. describe an elastocaloric cooling system with two essential new features: a cam-driven mechanism reducing the overall size of the system and NiTi elastocaloric tubes with fin inner structures enabling a much better heat exchange.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101960"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144098586","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}
JoulePub Date : 2025-05-21DOI: 10.1016/j.joule.2025.101878
Yeyang Jia , Zhilong Wang , Zhiyuan Han , Junfeng Li , Mengtian Zhang , Zhoujie Lao , Yanqiang Han , Runhua Gao , Jing Gao , Zhiyang Zheng , An Chen , Hong Li , Rui Mao , Kehao Tao , Jinjin Li , Guangmin Zhou
{"title":"Variable and intelligent catalyst design based on local chemical environments in sulfur redox reactions","authors":"Yeyang Jia , Zhilong Wang , Zhiyuan Han , Junfeng Li , Mengtian Zhang , Zhoujie Lao , Yanqiang Han , Runhua Gao , Jing Gao , Zhiyang Zheng , An Chen , Hong Li , Rui Mao , Kehao Tao , Jinjin Li , Guangmin Zhou","doi":"10.1016/j.joule.2025.101878","DOIUrl":"10.1016/j.joule.2025.101878","url":null,"abstract":"<div><div>The conventional constant catalyst design approach demonstrates limited adaptability to external conditions, impairing the catalytic performance in practical lithium-sulfur (Li-S) batteries. Here, we propose a variable and intelligent catalyst design strategy based on catalysts’ local chemical environments (LCEs). The competing adsorption between polysulfides and solvents within LCEs governs the interfacial reactions, regulated by the interaction between extrinsic electrolyte effects and intrinsic catalyst structures. Using nickel sulfides as a model system, interpretable machine-learning methods provide intelligent insights into structural tuning. Reversed catalytic efficiency is observed in LCEs of diluted and concentrated polysulfides, and variable catalyst modification guidance is presented for accelerating electron and ion transfer rates, respectively. Li-S batteries based on a Ni<sub>3</sub>S<sub>2</sub> catalyst manifest exceptional performance in a lean electrolyte, achieving an energy density of 433 Wh kg<sup>−1</sup> in pouch cells. This investigation provides a thorough design protocol for catalysts and promotes practical applications of Li-S batteries through catalytic conversion.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101878"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143666091","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}
JoulePub Date : 2025-05-21DOI: 10.1016/j.joule.2025.101919
Xuejie Zhu , Dongqi Yu , Xin Zhou , Nan Wang , Hong Liu , Zihui Liang , Congcong Wu , Kai Wang , Dayong Jin , Shengzhong Liu (Frank) , Dong Yang
{"title":"Interfacial molecular anchor for ambient all-bladed perovskite solar modules","authors":"Xuejie Zhu , Dongqi Yu , Xin Zhou , Nan Wang , Hong Liu , Zihui Liang , Congcong Wu , Kai Wang , Dayong Jin , Shengzhong Liu (Frank) , Dong Yang","doi":"10.1016/j.joule.2025.101919","DOIUrl":"10.1016/j.joule.2025.101919","url":null,"abstract":"<div><div>Ambient blade coating of perovskite solar modules shows great potential for large-scale manufacture and commercialization. However, blade coating nanometer-thick buffer layers typically results in a nonuniform surface due to particle instability and aggregation, often leading to insufficient integration and destabilization of the crystallographic lattice in the overlying perovskite layer. Herein, we introduce a layer of “molecular glue” that can effectively anchor the solute that suspends the monodisperse SnO<sub>2</sub> nanoparticles into a uniform thin film and adhere it to the top perovskite during the mechanical blading process. Leveraging this holistic nanoparticle-anchoring strategy, we have achieved a seamlessly bonded cathode heterojunction, resulting in a record efficiency of 26.11% for small cells and the highest efficiency so far of 22.76% (certified at 21.60%) for mini-modules. Importantly, these ambiently all-blade-coated devices exhibit an extended lifetime of approximately 1,500 h, as verified by ISOS-O testing, indicating great promise for commercialization.</div></div>","PeriodicalId":343,"journal":{"name":"Joule","volume":"9 5","pages":"Article 101919"},"PeriodicalIF":38.6,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143827397","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}