Transition metal small clusters anchored on biphenylene for effective electrocatalytic nitrogen reduction

被引:3
|
作者
Gao, Yan [1 ,2 ]
Li, Qingchen [2 ]
Yin, Zhilii [1 ]
Wang, Haifeng [2 ]
Wei, Zhong [1 ]
Gao, Junfeng [3 ]
机构
[1] Shihezi Univ, Sch Chem & Chem Engn, Shihezi 832003, Peoples R China
[2] Shihezi Univ, Coll Sci, Dept Phys, Shihezi 832003, Peoples R China
[3] Dalian Univ Technol, Key Lab Mat Modificat Laser Ion & Electron Beams, Minist Educ, Dalian 116024, Peoples R China
基金
中国国家自然科学基金;
关键词
AMMONIA-SYNTHESIS; SINGLE; CATALYSTS; EVOLUTION; FIXATION; GRAPHENE; CARBON; ATOMS;
D O I
10.1039/d3cp05763a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis of ammonia via an electrochemical nitrogen reduction reaction (NRR, N2 + 6H+ + 6e- -> 2NH3), which can weaken but not directly break an inert N 00000000000000000 00000000000000000 00000000000000000 01111111111111110 00000000000000000 01111111111111110 00000000000000000 01111111111111110 00000000000000000 00000000000000000 00000000000000000 N bond under mild conditions via multiple progressive protonation steps, has been proposed as one of the most attractive alternatives for the production of NH3. However, the development of appropriate catalyst materials is a major challenge in the application of NRRs. Recently, single- or multi-metal atoms anchored on two-dimensional (2D) substrates have been demonstrated as ideal candidates for facilitating NRRs. In this work, by applying spin-polarized density functional theory and ab initio molecular dynamic simulations, we systematically explored the performances of nine types of transition metal multi-atoms anchored on a recently developed 2D biphenylene (BPN) sheet in nitrogen reduction. Structural stability and NRR performance catalyzed by TMn (TM = V, Fe, Ni, Mo, Ru, Rh, W, Re, Ir; n = 1-4) clusters anchored on BPN sheets were systematically explored. After a strict six-step screening strategy, it was found that W2, Ru2 and Mo4 clusters loaded on BPN demonstrate superior potential for nitrogen reduction with extremely low onset potentials of -0.26, -0.36 and -0.17 V, respectively. Electronic structure analysis revealed that the enhanced ability of these multi-atom catalysts to effectively capture and reduce the N2 molecule can be attributed to bidirectional charge transfer between the d orbitals of transition metal atoms and molecular orbitals of the adsorbed N2 through a "donation-back donation" mechanism. Our findings highlight the value of BPN sheets as a substrate for designing multi-atom nitrogen reduction reaction catalysts. Scheme of transition metal small clusters TMn (TM = V, Fe, Ni, Mo, Ru, Rh, W, Re, Ir; n = 1-4) anchored on biphenylene for effective electrocatalytic nitrogen reduction.
引用
收藏
页码:6991 / 7000
页数:10
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