Rapid flipping between electrolyte and metallic states in ammonia solutions of alkali metals

被引:0
作者
Vitek, Marco [1 ]
Roncevic, Igor [1 ,2 ,3 ]
Marsalek, Ondrej [4 ]
Schewe, H. Christian [1 ,5 ]
Jungwirth, Pavel [1 ]
机构
[1] Czech Acad Sci, Inst Organ Chem & Biochem, Flemingovo Nam 2, Prague 6, Czech Republic
[2] Univ Oxford, Dept Chem, Chem Res Lab, Mansfield Rd, Oxford OX1 3TA, England
[3] Univ Manchester, Dept Chem, Oxford Rd, Manchester M13 9PL, England
[4] Charles Univ Prague, Fac Math & Phys, Ke Karlovu 3, Prague 2, Czech Republic
[5] Czech Acad Sci, J Heyrovsky Inst Phys Chem, Dolejskova 3, Prague 18223, Czech Republic
基金
欧盟地平线“2020”;
关键词
GENERALIZED GRADIENT APPROXIMATION; TOTAL-ENERGY CALCULATIONS; NONMETAL TRANSITION; MOLECULAR-DYNAMICS; LIQUID; LITHIUM; SEMICONDUCTORS; FLUCTUATIONS; SCATTERING;
D O I
10.1038/s41467-025-59071-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nonmetal-to-metal transitions are among the most fascinating phenomena in material science, associated with strong correlations, large fluctuations, and related features relevant to applications in electronics, spintronics, and optics. Dissolving alkali metals in liquid ammonia results in the formation of solvated electrons, which are localised in dilute solutions but exhibit metallic behaviour at higher concentrations, forming a disordered liquid metal. The electrolyte-to-metal transition in these systems appears to be gradual, but its microscopic origins remain poorly understood. Here, we provide a detailed time-resolved picture of the electrolyte-to-metal transition in solutions of lithium in liquid ammonia, employing ab initio molecular dynamics and many-body perturbation theory, which are validated against photoelectron spectroscopy experiments. We find a rapid flipping between metallic and electrolyte states that persist only on a sub-picosecond timescale within a broad range of concentrations. These flips, occurring within femtoseconds, are characterised by abrupt opening and closing of the band gap, which is connected with only minute changes in the solution structure and the associated electron density.
引用
收藏
页数:8
相关论文
共 56 条
[1]   Toward reliable density functional methods without adjustable parameters: The PBE0 model [J].
Adamo, C ;
Barone, V .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (13) :6158-6170
[2]   Electronic Levels of Excess Electrons in Liquid Water [J].
Ambrosio, Francesco ;
Miceli, Giacomo ;
Pasquarello, Alfredo .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2017, 8 (09) :2055-2059
[3]   Ab Initio Molecular Dynamics Simulations of Solvated Electrons in Ammonia Clusters [J].
Baranyi, Bence ;
Turi, Laszlo .
JOURNAL OF PHYSICAL CHEMISTRY B, 2020, 124 (33) :7205-7216
[4]   GROMACS - A MESSAGE-PASSING PARALLEL MOLECULAR-DYNAMICS IMPLEMENTATION [J].
BERENDSEN, HJC ;
VANDERSPOEL, D ;
VANDRUNEN, R .
COMPUTER PHYSICS COMMUNICATIONS, 1995, 91 (1-3) :43-56
[5]   REDUCTION BY DISSOLVING METALS .3. [J].
BIRCH, AJ .
JOURNAL OF THE CHEMICAL SOCIETY, 1946, (JUL) :593-597
[6]   Band gaps of liquid water and hexagonal ice through advanced electronic-structure calculations [J].
Bischoff, Thomas ;
Reshetnyak, Igor ;
Pasquarello, Alfredo .
PHYSICAL REVIEW RESEARCH, 2021, 3 (02)
[7]   PROJECTOR AUGMENTED-WAVE METHOD [J].
BLOCHL, PE .
PHYSICAL REVIEW B, 1994, 50 (24) :17953-17979
[8]  
Burns Gerald., 2013, Solid State Physics
[9]   Photoelectron spectra of alkali metal-ammonia microjets: From blue electrolyte to bronze metal [J].
Buttersack, Tillmann ;
Mason, Philip E. ;
McMullen, Ryan S. ;
Schewe, H. Christian ;
Martinek, Tomas ;
Brezina, Krystof ;
Crhan, Martin ;
Gomez, Axel ;
Hein, Dennis ;
Wartner, Garlef ;
Seidel, Robert ;
Ali, Hebatallah ;
Thurmer, Stephan ;
Marsalek, Ondrej ;
Winter, Bernd ;
Bradforth, Stephen E. ;
Jungwirth, Pavel .
SCIENCE, 2020, 368 (6495) :1086-+
[10]   Birth of the Hydrated Electron via Charge-Transfer-to-Solvent Excitation of Aqueous Iodide [J].
Carter-Fenk, Kevin ;
Johnson, Britta A. ;
Herbert, John M. ;
Schenter, Gregory K. ;
Mundy, Christopher J. .
JOURNAL OF PHYSICAL CHEMISTRY LETTERS, 2023, 14 (04) :870-878