Guo Hongyun, Fu Xiaoxiao, Peng Lishan, Wang Chaobo, Zhuang Yujuan, Chong He, Chen Zhaohui, Gong Weijiang, Yan Mi, Wang Qiang, Cui Weibin
Key Laboratory of Electromagnetic Processing of Materials, Ministry of Education, Northeastern University, Shenyang, 110819, China.
International Joint Laboratory for Light Alloys (MOE), College of Materials Science and Engineering, Chongqing University, Chongqing, 400044, China.
Adv Mater. 2024 Sep;36(36):e2404466. doi: 10.1002/adma.202404466. Epub 2024 Jul 28.
Nanolamellar transition metal carbides are gaining increasing attentions because of the promising application in energy storage of their 2D derivatives. There are in-plane and out-of-plane atomic ordered occupations, which is thought to only be formed in separated systems due to totally different origins and crystallographic structure. In present work, starting from (Mo, Nb)AlC o-MAX phase where out-of-plane ordered occupation is experimentally and theoretically proved for Mo/Nb atoms, rare-earth elements (R = Y, Gd-Tm, Lu) are introduced, and the novel Mo RNbAlC (x = 1, 1.25, 1.5, 1.75, 2, 2.25, and 2.5) super-ordered (s-) MAX phase is synthesized, where R is ordered at the outer layer in the strict stoichiometry meanwhile Mo/Nb maintains the out-of-plane ordered occupation. By R introduction, s-MAX is easier to be delaminated to obtain the s-MXene with the topochemical ordered vacancies, leading into the enhanced supercapacitance of 114.9 F g in MoNbC s-MXene compared with 95.1 F g in MoNbC o-MXene. By Pt anchoring, very low overpotential of 22 mV at a current density of 10 mA cm is achieved for HER applications. This study demonstrates a novel variety of s-MAX phase and seeks to inspire further exploration of the ordered MAX and MXene families.
纳米层状过渡金属碳化物因其二维衍生物在能量存储方面的应用前景而受到越来越多的关注。存在面内和面外原子有序占据情况,由于其完全不同的起源和晶体结构,人们认为这种情况仅在分离的体系中形成。在本工作中,从(Mo,Nb)AlC 有序MAX相出发,其中通过实验和理论证明了Mo/Nb原子的面外有序占据,引入稀土元素(R = Y、Gd - Tm、Lu),合成了新型的MoRNbAlC(x = 1、1.25、1.5、1.75、2、2.25和2.5)超有序(s-)MAX相,其中R以严格的化学计量比在外层有序排列,同时Mo/Nb保持面外有序占据。通过引入R,s-MAX更容易分层以获得具有拓扑化学有序空位的s-MXene,与MoNbC 有序MXene中95.1 F g的比电容相比,MoNbC s-MXene的比电容提高到114.9 F g。通过Pt锚定,在HER应用中,在电流密度为10 mA cm时实现了仅22 mV的极低过电位。本研究展示了一种新型的s-MAX相,并旨在激发对有序MAX和MXene家族的进一步探索。