Nature EnergyPub Date : 2024-06-21DOI: 10.1038/s41560-024-01582-y
Si Wu, Tingxian Li
{"title":"Author Correction: Taking control of salts","authors":"Si Wu, Tingxian Li","doi":"10.1038/s41560-024-01582-y","DOIUrl":"10.1038/s41560-024-01582-y","url":null,"abstract":"","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s41560-024-01582-y.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142045352","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}
{"title":"Achieving 19% efficiency in non-fused ring electron acceptor solar cells via solubility control of donor and acceptor crystallization","authors":"Rui Zeng, Ming Zhang, Xiaodong Wang, Lei Zhu, Bonan Hao, Wenkai Zhong, Guanqing Zhou, Jiawei Deng, Senke Tan, Jiaxin Zhuang, Fei Han, Anyang Zhang, Zichun Zhou, Xiaonan Xue, Shengjie Xu, Jinqiu Xu, Yahui Liu, Hao Lu, Xuefei Wu, Cheng Wang, Zachary Fink, Thomas P. Russell, Hao Jing, Yongming Zhang, Zhishan Bo, Feng Liu","doi":"10.1038/s41560-024-01564-0","DOIUrl":"https://doi.org/10.1038/s41560-024-01564-0","url":null,"abstract":"<p>Non-fused ring electron acceptors (NFREAs) potentially have lower synthetic costs than their fused counterparts. However, the low backbone planarity and the presence of bulky substituents adversely affect the crystallinity of NFREAs, impeding charge transport and the formation of bicontinuous morphology in organic solar cells. Here we show that a binary solvent system can individually control the crystallization and phase separation of the donor polymer (for example, D18) and the NFREA (for example, 2BTh-2F-C<sub>2</sub>). We select solvents such as chloroform and <i>o</i>-xylene that evaporate at different temperatures and rates and have different solubility for D18. Upon evaporation of chloroform, D18 starts to assemble into fibrils. Then, the evaporation of <i>o</i>-xylene induces the rapid formation of a fibril network that phase segregates 2BTh-2F-C<sub>2</sub> into pure domains and leads to a bicontinuous morphology. The well-defined interpenetrating network morphology affords an efficiency of 19.02% on small-area cells and 17.28% on 1 cm<sup>2</sup> devices.</p>","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":56.7,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141435889","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}
Nature EnergyPub Date : 2024-06-21DOI: 10.1038/s41560-024-01563-1
Kiane de Kleijne, Mark A. J. Huijbregts, Florian Knobloch, Rosalie van Zelm, Jelle P. Hilbers, Heleen de Coninck, Steef V. Hanssen
{"title":"Worldwide greenhouse gas emissions of green hydrogen production and transport","authors":"Kiane de Kleijne, Mark A. J. Huijbregts, Florian Knobloch, Rosalie van Zelm, Jelle P. Hilbers, Heleen de Coninck, Steef V. Hanssen","doi":"10.1038/s41560-024-01563-1","DOIUrl":"https://doi.org/10.1038/s41560-024-01563-1","url":null,"abstract":"<p>Large-scale introduction of green hydrogen is envisioned to play an important role in reaching net-zero greenhouse gas emissions. The production and transport of green hydrogen itself is, however, not free from emissions. Here we assess the life-cycle greenhouse gas emissions for 1,025 planned green hydrogen facilities, covering different electrolyser technologies and renewable electricity sources in 72 countries. We demonstrate that the current exclusion of life-cycle emissions of renewables, component manufacturing and hydrogen leakage in regulations gives a false impression that green hydrogen can easily meet emission thresholds. Evaluating different hydrogen production configurations, we find median production emissions in the most optimistic configuration of 2.9 kg CO<sub>2</sub> equivalents (CO<sub>2</sub>e) kg H<sub>2</sub><sup>−1</sup> (0.8–4.6 kgCO<sub>2</sub>e kg H<sub>2</sub><sup>−1</sup>, 95% confidence interval). Including 1,000 km transport via pipeline or liquid hydrogen shipping adds another 1.5 or 1.8 kgCO<sub>2</sub>e kg H<sub>2</sub><sup>−1</sup>, respectively. We conclude that achieving low-emission green hydrogen at scale requires well-chosen production configurations with substantial emission reductions along the supply chain.</p>","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":56.7,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141435890","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}
Nature EnergyPub Date : 2024-06-18DOI: 10.1038/s41560-024-01545-3
Joanna Sitarz, Michael Pahle, Sebastian Osorio, Gunnar Luderer, Robert Pietzcker
{"title":"Policy credibility is a key component for an effective and efficient EU Emissions Trading System","authors":"Joanna Sitarz, Michael Pahle, Sebastian Osorio, Gunnar Luderer, Robert Pietzcker","doi":"10.1038/s41560-024-01545-3","DOIUrl":"10.1038/s41560-024-01545-3","url":null,"abstract":"Recent reforms of the EU Emissions Trading System (EU ETS) boosted carbon prices by tightening the cap on emission allowances and increasing political commitment to it, which effectively made actors more farsighted. Policymakers should thus view prices as an indicator of credibility as well as scarcity, and manage potential future drops in the former by renewing commitment to the cap.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s41560-024-01545-3.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141334237","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}
Nature EnergyPub Date : 2024-06-18DOI: 10.1038/s41560-024-01554-2
Kathleen M. Kennedy, Morgan R. Edwards, Claudia Doblinger, Zachary H. Thomas, Maria A. Borrero, Ellen D. Williams, Nathan E. Hultman, Kavita Surana
{"title":"Rapid rise in corporate climate-tech investments complements support from public grants","authors":"Kathleen M. Kennedy, Morgan R. Edwards, Claudia Doblinger, Zachary H. Thomas, Maria A. Borrero, Ellen D. Williams, Nathan E. Hultman, Kavita Surana","doi":"10.1038/s41560-024-01554-2","DOIUrl":"10.1038/s41560-024-01554-2","url":null,"abstract":"Investment in climate and energy (climate-tech) startups is growing in the US and worldwide, with public grants backing high-risk sectors and publicly funded startups exiting at higher rates with corporate investment. Public policies to incentivize corporate investment in these startups can therefore be an important, yet sometimes underestimated, part of meeting net-zero goals.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s41560-024-01554-2.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141334369","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}
Nature EnergyPub Date : 2024-06-18DOI: 10.1038/s41560-024-01555-1
Steffen Link, Annegret Stephan, Daniel Speth, Patrick Plötz
{"title":"Declining costs imply fast market uptake of zero-emission trucks","authors":"Steffen Link, Annegret Stephan, Daniel Speth, Patrick Plötz","doi":"10.1038/s41560-024-01555-1","DOIUrl":"10.1038/s41560-024-01555-1","url":null,"abstract":"Zero-emission trucks will benefit from rapidly falling costs of batteries and fuel cells, which will enable their fast market diffusion. Industry and policy must prepare for battery-electric trucks with respect to their manufacturing and supply, adequate charging infrastructure and electricity grid expansions, as well as regulation.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.nature.com/articles/s41560-024-01555-1.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141334228","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}
{"title":"Non-fullerene acceptor with asymmetric structure and phenyl-substituted alkyl side chain for 20.2% efficiency organic solar cells","authors":"Yuanyuan Jiang, Shaoming Sun, Renjie Xu, Feng Liu, Xiaodan Miao, Guangliu Ran, Kerui Liu, Yuanping Yi, Wenkai Zhang, Xiaozhang Zhu","doi":"10.1038/s41560-024-01557-z","DOIUrl":"10.1038/s41560-024-01557-z","url":null,"abstract":"For organic solar cells (OSCs), bridging the gap with Shockley–Queisser limit necessitates simultaneously reducing the energy loss for a high open-circuit voltage, improving light utilization for enhanced short-circuit current density and maintaining ideal nanomorphology with a high fill factor through molecular design and device engineering. Here we design and synthesize an asymmetric non-fullerene acceptor (Z8) featuring tethered phenyl groups to establish an alloy acceptor in ternary OSCs. The asymmetric structure minimizes non-radiative energy loss and charge recombination owing to delocalized excitons. The phenyl-substituted alkyl side chain impacts on the intermolecular interactions, improving the film nanomorphology with efficient exciton dissociation and reduced charge recombination. We demonstrate OSCs with an efficiency of 20.2% (certified 19.8%) based on the D18:Z8:L8-BO ternary blend. Through theoretical calculations, we examine the overall distribution of photon and carrier losses and analyse the potential for improvement on open-circuit voltage, short-circuit current density and fill factor, providing rational guidance for further development of the OSC performance. Molecular design is key to the power conversion efficiency in organic photovoltaics. Jiang, Sun, Xu et al. develop a non-fullerene acceptor with asymmetric structure and phenyl-substituted side chains that minimizes photon and carrier losses, enabling 20.2% efficiency.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141309133","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}
Nature EnergyPub Date : 2024-06-11DOI: 10.1038/s41560-024-01556-0
Kuang-Jung Hsu, Shaoxian Li, Marina Micari, Heng-Yu Chi, Luis Francisco Villalobos, Shiqi Huang, Liping Zhong, Shuqing Song, Xuekui Duan, Andreas Züttel, Kumar Varoon Agrawal
{"title":"Graphene membranes with pyridinic nitrogen at pore edges for high-performance CO2 capture","authors":"Kuang-Jung Hsu, Shaoxian Li, Marina Micari, Heng-Yu Chi, Luis Francisco Villalobos, Shiqi Huang, Liping Zhong, Shuqing Song, Xuekui Duan, Andreas Züttel, Kumar Varoon Agrawal","doi":"10.1038/s41560-024-01556-0","DOIUrl":"10.1038/s41560-024-01556-0","url":null,"abstract":"Membranes based on a porous two-dimensional selective layer offer the potential to achieve exceptional performance to improve energy efficiency and reduce the cost for carbon capture. So far, separation from two-dimensional pores has exploited differences in molecular mass or size. However, competitive sorption of CO2 with the potential to yield high permeance and selectivity has remained elusive. Here we show that a simple exposure of ammonia to oxidized single-layer graphene at room temperature incorporates pyridinic nitrogen at the pore edges. This leads to a highly competitive but quantitatively reversible binding of CO2 with the pore. An attractive combination of CO2/N2 separation factor (average of 53) and CO2 permeance (average of 10,420) from a stream containing 20 vol% CO2 is obtained. Separation factors above 1,000 are achieved for dilute (~1 vol%) CO2 stream, making the membrane promising for carbon capture from diverse point emission sources. Thanks to the uniform and scalable chemistry, high-performance centimetre-scale membranes are demonstrated. The scalable preparation of high-performance two-dimensional membranes opens new directions in membrane science. Graphene-based membranes are attractive for capturing CO2, with separation selectivity typically achieved by control of pore size. Here Hsu et al. incorporate pyridinic nitrogen species at the pore edges in graphene, leading to competitive CO2 binding and enhanced separation performance.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141304378","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}
Nature EnergyPub Date : 2024-06-07DOI: 10.1038/s41560-024-01538-2
Xiyang Cai, Junliang Zhang
{"title":"Solvent effects in Li-mediated synthesis","authors":"Xiyang Cai, Junliang Zhang","doi":"10.1038/s41560-024-01538-2","DOIUrl":"10.1038/s41560-024-01538-2","url":null,"abstract":"Electrochemical ammonia (NH3) synthesis is a promising alternative to the Haber–Bosch process, but higher-performing systems are needed. Now, researchers realize long-term continuous NH3 electrosynthesis and production of high fractions of gas-phase NH3 by employing a chain ether as solvent, marking an important practical step forward.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141287277","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}
Nature EnergyPub Date : 2024-06-06DOI: 10.1038/s41560-024-01541-7
Rui Song, Guanshu Zhao, Juan Manuel Restrepo-Flórez, Camilo J. Viasus Pérez, Zhijie Chen, Chaoqian Ai, Andrew Wang, Dengwei Jing, Athanasios A. Tountas, Jiuli Guo, Chengliang Mao, Chaoran Li, Jiahui Shen, Guangming Cai, Chenyue Qiu, Jessica Ye, Yubin Fu, Chistos T. Maravelias, Lu Wang, Junchuan Sun, Yang-Fan Xu, Zhao Li, Joel Yi Yang Loh, Nhat Truong Nguyen, Le He, Xiaohong Zhang, Geoffrey A. Ozin
{"title":"Ethylene production via photocatalytic dehydrogenation of ethane using LaMn1−xCuxO3","authors":"Rui Song, Guanshu Zhao, Juan Manuel Restrepo-Flórez, Camilo J. Viasus Pérez, Zhijie Chen, Chaoqian Ai, Andrew Wang, Dengwei Jing, Athanasios A. Tountas, Jiuli Guo, Chengliang Mao, Chaoran Li, Jiahui Shen, Guangming Cai, Chenyue Qiu, Jessica Ye, Yubin Fu, Chistos T. Maravelias, Lu Wang, Junchuan Sun, Yang-Fan Xu, Zhao Li, Joel Yi Yang Loh, Nhat Truong Nguyen, Le He, Xiaohong Zhang, Geoffrey A. Ozin","doi":"10.1038/s41560-024-01541-7","DOIUrl":"10.1038/s41560-024-01541-7","url":null,"abstract":"Industrial-scale ethylene production occurs primarily by fossil-powered steam cracking of ethane—a high-temperature, high-energy process. An alternative, photochemical, pathway powered by sunlight and operating under ambient conditions could potentially mitigate some of the associated greenhouse gas emissions. Here we report the photocatalytic dehydrogenation of ethane to ethylene and hydrogen using LaMn1−xCuxO3. This perovskite oxide possesses redox-active Lewis acid sites, comprising Mn(III) and Mn(IV), and Lewis base sites, comprising O(-II) and OH(-I), collectively dubbed surface-frustrated Lewis pairs. We find that tuning the relative proportions of these sites optimizes the activity, selectivity and yield for ethane dehydrogenation. The highest ethylene production rate and ethane conversion achieved were around 1.1 mmol g−1 h−1 and 4.9%, respectively. We show a simple outdoor prototype to demonstrate the viability of a solar ethylene process. In addition, techno-economic analysis revealed the economic potential of an industrial-scale solar ethylene production from ethane. Light-driven approaches could lower the carbon footprint of chemical production. Here the authors use the perovskite oxide LaMn1−xCuxO3 as a photocatalyst to convert ethane to ethylene and hydrogen.","PeriodicalId":19073,"journal":{"name":"Nature Energy","volume":null,"pages":null},"PeriodicalIF":49.7,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141264759","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}