Lin Yun-Xiao, Feng Wei-Jie, Zhang Jun-Jun, Xue Zhong-Hua, Zhao Tian-Jian, Su Hui, Hirano Shin-Ichi, Li Xin-Hao, Chen Jie-Sheng
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, 200240, P. R. China.
Hirano Institute for Materials Innovation, Shanghai Jiao Tong University, Shanghai, 200240, P. R. China.
Angew Chem Int Ed Engl. 2018 Sep 17;57(38):12563-12566. doi: 10.1002/anie.201808036. Epub 2018 Aug 27.
The exploitation of metal-free organic polymers as electrodes for water splitting reactions is limited by their presumably low activity and poor stability, especially for the oxygen evolution reaction (OER) under more critical conditions. Now, the thickness of a cheap and robust polymer, poly(p-phenylene pyromellitimide) (PPPI) was rationally engineered by an in situ polymerization method to make the metal-free polymer available for the first time as flexible, tailorable, efficient, and ultra-stable electrodes for water oxidation over a wide pH range. The PPPI electrode with an optimized thickness of about 200 nm provided a current density of 32.8 mA cm at an overpotential of 510 mV in 0.1 mol L KOH, which is even higher than that (31.5 mA cm ) of commercial IrO OER catalyst. The PPPI electrodes are scalable and stable, maintaining 92 % of its activity after a 48-h chronoamperometric stability test.
无金属有机聚合物作为析水反应电极的应用受到其活性可能较低以及稳定性较差的限制,特别是在更苛刻条件下的析氧反应(OER)中。现在,通过原位聚合法合理设计了一种廉价且坚固的聚合物——聚对苯二甲酰对苯二胺酰亚胺(PPPI)的厚度,首次使这种无金属聚合物可作为在宽pH范围内用于水氧化的柔性、可定制、高效且超稳定的电极。优化厚度约为200 nm的PPPI电极在0.1 mol·L KOH中,过电位为510 mV时提供了32.8 mA·cm的电流密度,甚至高于商业IrO OER催化剂的电流密度(31.5 mA·cm)。PPPI电极具有可扩展性且稳定,在48小时的计时电流稳定性测试后仍保持其活性的92%。