Huang Chun-Lung, Chuah Xui-Fang, Hsieh Cheng-Ting, Lu Shih-Yuan
Department of Chemical Engineering , National Tsing Hua University , Hsinchu 30013 , Taiwan.
ACS Appl Mater Interfaces. 2019 Jul 10;11(27):24096-24106. doi: 10.1021/acsami.9b05919. Epub 2019 Jun 24.
A bubble-releasing assisted pulse electrodeposition method was developed to create metallic alloy, NiFe, nanotube arrays in one step. The NiFe alloy nanotube array exhibited excellent bifunctional electrolytic activities, achieving low overpotentials of 100 mV for the hydrogen evolution reaction and 236 mV for the oxygen evolution reaction at 10 mA cm, both in 1 M KOH at room temperature. For overall water splitting, the NiFe alloy nanotube array delivered 10 mA cm at an ultralow cell voltage of 1.58 V, among the top tier of the state-of-the-art bifunctional electrocatalysts. The NiFe alloy nanotube array also exhibited ultrastability at high current densities, experiencing only a minor chronoamperometric decay of 6.5% after a 24 h operation at 400 mA cm. The success of the present binder-free nanotube array-based electrode can be attributed to the much enlarged reaction surface area, one-dimensionally guided charge transport and mass transfer offered by the nanotube structure, and improved product crystallinity provided by the pulse current electrodeposition. The nanotube array structure proves to be a promising new architecture design for electrocatalysts.
开发了一种气泡释放辅助脉冲电沉积方法,可一步制备金属合金NiFe纳米管阵列。在室温下的1 M KOH溶液中,NiFe合金纳米管阵列表现出优异的双功能电解活性,在10 mA cm下析氢反应的过电位低至100 mV,析氧反应的过电位低至236 mV。对于全水解,NiFe合金纳米管阵列在1.58 V的超低电池电压下实现了10 mA cm的电流密度,跻身最先进的双功能电催化剂之列。NiFe合金纳米管阵列在高电流密度下也表现出超高稳定性,在400 mA cm下运行24小时后,计时电流衰减仅为6.5%。这种无粘结剂的纳米管阵列基电极的成功可归因于纳米管结构提供的大大扩大的反应表面积、一维引导的电荷传输和质量传输,以及脉冲电流电沉积提供的改善的产物结晶度。纳米管阵列结构被证明是一种很有前途的电催化剂新结构设计。