Yuanyuan ZhengAmanda Schramm PetersenHao WanRené HübnerJiangwei ZhangJianlan WangHaoyuan QiYuhong YeChaolun LiangJing YangZhiming CuiYuezhong MengZhikun ZhengJan RossmeislWei Liu
Abstract Developing efficient and stable Pt‐based oxygen reduction reaction (ORR) electrocatalysts via both economical and controllable routes is critical for the practical application of electrochemical energy devices. Herein, a scalable, controllable, and general ambient‐O 2 ‐involved aqueous‐solution cultivating strategy to prepare Pt x M y (M = Ni, Fe, Co) bunched‐nanocages aerogels (BNCs AG) is demonstrated, based on a newly established high‐M‐to‐Pt‐precursor‐ratio‐and‐B‐incorporation‐facilitated M‐rich core and Pt‐rich shell hydrogel formation process. The Pt 83 Ni 17 BNCs AG shows prominent ORR performance with a mass activity (MA) of 1.95 A mg Pt −1 and specific activity of 3.55 mA cm −2 , which are 8.9‐times and 9.6‐times that of Pt supported on carbon (Pt/C), respectively. Particularly, the Pt 83 Ni 17 BNCs AG displays greatly enhanced durability (MA 82.6% retention) compared to Pt/C (MA 31.8% retention) after a 20 000‐cycles accelerated durability test. Systematic studies including density functional theory calculations uncover that the excellent activity is closely related to the optimized ligand and strain effects with the optimized Ni content in this aerogel; the outstanding durability is endowed by the lowered‐down Ni leaching with the optimized Pt/Ni ratio and the inhibited sintering due to its appropriate porosity. This work provides new perspectives on the development of electrocatalysts with both high performance and low cost.
Sebastian HenningLaura KühnJuan HerranzJulien DurstTobias BinningerMaarten NachtegaalMatthias WerheidWei LiuMarion AdamStefan KaskelAlexander EychmüllerThomas J. Schmidt
Xinlong TianXiao ZhaoYaqiong SuLijuan WangHongming WangDai DangBin ChiHongfang LiuEmiel J. M. HensenXiong Wen LouBao Yu Xia
Qiaowan ChangYuan XuShangqian ZhuFei XiaoMinhua Shao
Sebastian HenningJuan HerranzLaura KühnAlexander EychmüllerThomas J. Schmidt