Li Baoyan
Department of Chemical Engineering, University College London, LondonWC1E 7JE,U.K.
ACS Omega. 2023 Sep 13;8(38):35077-35084. doi: 10.1021/acsomega.3c04605. eCollection 2023 Sep 26.
Recently, graphdiyne (GDY) as a two-dimensional planar carbon allotrope has received significant research attention in the fields of rechargeable batteries, catalysis, biomedicine, and so forth. However, the theoretical capacity of a perfect GDY anode is only 744 mA h/g in the configuration of LiC, encouraging further efforts to increase the capacity. In this study, we explore the anode performance of N-, P-, and As-doped GDYs by using first-principles calculations. Ab initio molecular dynamics simulations show that the doped GDYs can remain stable at 1000 K, indicating good thermal stability. With the loss of part acetylenic linkages, the rhomboid-like pores produce more Li sites, and the theoretical capacities reach 2209, 2031, and 1681 mA h/g for the N-, P-, and As-doped GDYs, respectively. In addition, the transition-state calculations indicate that the Li diffusion barriers of the three doped GDYs are similar to the perfect GDY. This study demonstrates that doping is an effective strategy to improve the anode performance of GDY.
最近,作为一种二维平面碳同素异形体的石墨炔(GDY)在可充电电池、催化、生物医学等领域受到了广泛的研究关注。然而,在LiC结构中,理想的GDY阳极理论容量仅为744 mA h/g,这促使人们进一步努力提高其容量。在本研究中,我们通过第一性原理计算探索了N、P和As掺杂的GDY的阳极性能。从头算分子动力学模拟表明,掺杂的GDY在1000 K时仍能保持稳定,具有良好的热稳定性。随着部分炔键的丢失,菱形孔产生了更多的锂位点,N、P和As掺杂的GDY的理论容量分别达到2209、2031和1681 mA h/g。此外,过渡态计算表明,三种掺杂的GDY的锂扩散势垒与理想的GDY相似。本研究表明,掺杂是提高GDY阳极性能的有效策略。