Guo Jiangnan, Liu Jinlong, Mao Xichen, Chu Shengqi, Zhang Xinxin, Luo Ziyu, Li Jie, Wang Bowen, Jia Chuankun, Qian Dong
College of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, China.
J Phys Chem Lett. 2022 Jun 6:5195-5203. doi: 10.1021/acs.jpclett.2c01040.
The identification of synergistic effect of Pt-based alloys on hydrogen evolution reaction (HER) requires a combination of experimental studies and theoretical calculations. Here, we present the construction of uniform PtCo nanoparticles grown on N-doped carbon frameworks via pyrolyzing Pt and Co ions adsorbed polyaniline, whereby the nanostructure of the nanoalloys can be effectively tuned by controlling the calcination temperature. As-prepared PtCo@NC-900 shows the optimal HER performance in 0.5 M HSO, resulting in a high mass activity of 4.31 A mg and excellent operation durability, which far exceeds that of commercial 20 wt % Pt/C (0.30 A mg). Density functional theory calculations further reveal that the improved HER activity on PtCo(111) is originated from the strong electronic interaction between Pt and Co with favorable electron transfer, allowing for a more suitable binding strength for hydrogen (i.e., Δ = -0.164 eV) compared with that of pristine Pt(111) (-0.287 eV).
确定铂基合金对析氢反应(HER)的协同效应需要结合实验研究和理论计算。在此,我们展示了通过热解吸附了铂和钴离子的聚苯胺,在氮掺杂碳骨架上生长均匀的铂钴纳米颗粒的过程,由此可以通过控制煅烧温度有效地调节纳米合金的纳米结构。所制备的PtCo@NC-900在0.5 M HSO中表现出最佳的析氢反应性能,产生了4.31 A mg的高质量活性和优异的操作耐久性,这远远超过了商业20 wt% Pt/C(0.30 A mg)。密度泛函理论计算进一步表明,PtCo(111)上析氢反应活性的提高源于铂和钴之间强烈的电子相互作用以及有利的电子转移,与原始Pt(111)(-0.287 eV)相比,使得氢的结合强度更合适(即Δ = -0.164 eV)。