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Health co-benefits of achieving sustainable net-zero greenhouse gas emissions in California 期刊论文
NATURE SUSTAINABILITY, 2020
作者:  Wang, Tianyang;  Jiang, Zhe;  Zhao, Bin;  Gu, Yu;  Liou, Kuo-Nan;  Kalandiyur, Nesamani;  Zhang, Da;  Zhu, Yifang
收藏  |  浏览/下载:8/0  |  提交时间:2020/05/13
Leverage points for sustainability transformation: a review on interventions in food and energy systems 期刊论文
ECOLOGICAL ECONOMICS, 2020, 171
作者:  Dorninger, Christian;  Abson, David J.;  Apetrei, Cristina I.;  Derwort, Pim;  Ives, Christopher D.;  Klaniecki, Kathleen;  Lam, David P. M.;  Langsenlehne, Maria;  Riechers, Maraja;  Spittler, Nathalie;  von Wehrden, Henrik
收藏  |  浏览/下载:8/0  |  提交时间:2020/07/02
Energy system  Food system  Leverage points  Sustainability interventions  Sustainability transformation  
The evolution of ideas in global climate policy 期刊论文
NATURE CLIMATE CHANGE, 2020, 10 (5) : 434-+
作者:  Meckling, Jonas;  Allan, Bentley B.
收藏  |  浏览/下载:9/0  |  提交时间:2020/05/13
Hydraulic Potential Energy Model for Hydropower Operation in Mixed Reservoir Systems 期刊论文
WATER RESOURCES RESEARCH, 2020, 56 (4)
作者:  Wan, Wenhua;  Wang, Hao;  Zhao, Jianshi
收藏  |  浏览/下载:7/0  |  提交时间:2020/07/02
Hydraulic potential energy  forecast-informed operation  energy transformation formula  relative marginal energy principle  two-stage hydraulic potential energy model  
A Sensitivity Study of Arctic Air-Mass Transformation Using Large Eddy Simulation 期刊论文
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2020, 125 (6)
作者:  Dimitrelos, Antonios;  Ekman, Annica M. L.;  Caballero, Rodrigo;  Savre, Julien
收藏  |  浏览/下载:7/0  |  提交时间:2020/07/02
Why ecological economics needs to return to its roots: The biophysical foundation of socio-economic systems 期刊论文
ECOLOGICAL ECONOMICS, 2020, 169
作者:  Melgar-Melgar, Rigo E.;  Hall, Charles A. S.
收藏  |  浏览/下载:14/0  |  提交时间:2020/07/02
Energy transitions  Biophysical economics  Ecological economics  Climate change  Sustainability  Green New Deal  Sustainable Development Goals  
Observations of grain-boundary phase transformations in an elemental metal 期刊论文
NATURE, 2020, 579 (7799) : 375-+
作者:  Valente, Luis;  Phillimore, Albert B.;  Melo, Martim;  Warren, Ben H.;  Clegg, Sonya M.;  Havenstein, Katja;  Tiedemann, Ralph;  Illera, Juan Carlos;  Thebaud, Christophe;  Aschenbach, Tina;  Etienne, Rampal S.
收藏  |  浏览/下载:16/0  |  提交时间:2020/07/03

Atomic-resolution observations combined with simulations show that grain boundaries within elemental copper undergo temperature-induced solid-state phase transformation to different structures  grain boundary phases can also coexist and are kinetically trapped structures.


The theory of grain boundary (the interface between crystallites, GB) structure has a long history(1) and the concept of GBs undergoing phase transformations was proposed 50 years ago(2,3). The underlying assumption was that multiple stable and metastable states exist for different GB orientations(4-6). The terminology '  complexion'  was recently proposed to distinguish between interfacial states that differ in any equilibrium thermodynamic property(7). Different types of complexion and transitions between complexions have been characterized, mostly in binary or multicomponent systems(8-19). Simulations have provided insight into the phase behaviour of interfaces and shown that GB transitions can occur in many material systems(20-24). However, the direct experimental observation and transformation kinetics of GBs in an elemental metal have remained elusive. Here we demonstrate atomic-scale GB phase coexistence and transformations at symmetric and asymmetric [111 over bar ] tilt GBs in elemental copper. Atomic-resolution imaging reveals the coexistence of two different structures at sigma 19b GBs (where sigma 19 is the density of coincident sites and b is a GB variant), in agreement with evolutionary GB structure search and clustering analysis(21,25,26). We also use finite-temperature molecular dynamics simulations to explore the coexistence and transformation kinetics of these GB phases. Our results demonstrate how GB phases can be kinetically trapped, enabling atomic-scale room-temperature observations. Our work paves the way for atomic-scale in situ studies of metallic GB phase transformations, which were previously detected only indirectly(9,15,27-29), through their influence on abnormal grain growth, non-Arrhenius-type diffusion or liquid metal embrittlement.


  
Single-pass transformation of syngas into ethanol with high selectivity by triple tandem catalysis 期刊论文
NATURE COMMUNICATIONS, 2020, 11 (1)
作者:  Kang, Jincan;  He, Shun;  Zhou, Wei;  Shen, Zheng;  Li, Yangyang;  Chen, Mingshu;  Zhang, Qinghong;  Wang, Ye
收藏  |  浏览/下载:8/0  |  提交时间:2020/05/13
Early transformation of the Chinese power sector to avoid additional coal lock-in 期刊论文
ENVIRONMENTAL RESEARCH LETTERS, 2020, 15 (2)
作者:  Wang, Huan;  Chen, Wenying;  Bertram, Christoph;  Malik, Aman;  Kriegler, Elmar;  Luderer, Gunnar;  Despres, Jacques;  Jiang, Kejun;  Krey, Volker
收藏  |  浏览/下载:11/0  |  提交时间:2020/07/02
China  power system  coal lock-in  stranded risks  WB2C target  
Conversion of non-van der Waals solids to 2D transition-metal chalcogenides 期刊论文
NATURE, 2020, 577 (7791) : 492-+
作者:  Du, Zhiguo;  Yang, Shubin;  Li, Songmei;  Lou, Jun;  Zhang, Shuqing;  Wang, Shuai;  Li, Bin;  Gong, Yongji;  Song, Li;  Zou, Xiaolong;  Ajayan, Pulickel M.
收藏  |  浏览/下载:7/0  |  提交时间:2020/07/03

A synthetic approach is described, for efficiently converting non-van der Waals solids into two-dimensional van der Waals transition-metal chalcogenide layers with specific phases, enabling the high-throughput production of monolayers.


Although two-dimensional (2D) atomic layers, such as transition-metal chalcogenides, have been widely synthesized using techniques such as exfoliation(1-3) and vapour-phase growth(4,5), it is still challenging to obtain phase-controlled 2D structures(6-8). Here we demonstrate an effective synthesis strategy via the progressive transformation of non-van der Waals (non-vdW) solids to 2D vdW transition-metal chalcogenide layers with identified 2H (trigonal prismatic)/1T (octahedral) phases. The transformation, achieved by exposing non-vdW solids to chalcogen vapours, can be controlled using the enthalpies and vapour pressures of the reaction products. Heteroatom-substituted (such as yttrium and phosphorus) transition-metal chalcogenides can also be synthesized in this way, thus enabling a generic synthesis approach to engineering phase-selected 2D transition-metal chalcogenide structures with good stability at high temperatures (up to 1,373 kelvin) and achieving high-throughput production of monolayers. We anticipate that these 2D transition-metal chalcogenides will have broad applications for electronics, catalysis and energy storage.