Kwon Hagyeong, Bae Dongyeon, Won Dongyeun, Kim Heeju, Kim Gunn, Cho Jiung, Park Hee Jung, Baik Hionsuck, Jeong Ah Reum, Lin Chia-Hsien, Chiang Ching-Yu, Ku Ching-Shun, Yang Heejun, Cho Suyeon
Division of Chemical Engineering and Materials Science, Graduate Program for System Health Science and Engineering (BK21 Plus), Ewha Womans University, Seoul 03760, Republic of Korea.
Department of Energy Science, Sungkyunkwan University, Suwon 16419, Republic of Korea.
ACS Nano. 2021 Apr 27;15(4):6540-6550. doi: 10.1021/acsnano.0c09517. Epub 2021 Mar 30.
Silver-based nanomaterials have been versatile building blocks of various photoassisted energy applications; however, they have demonstrated poor electrochemical catalytic performance and stability, in particular, in acidic environments. Here we report a stable and high-performance electrochemical catalyst of silver telluride (AgTe) for the hydrogen evolution reaction (HER), which was synthesized with a nanoporous structure by an electrochemical synthesis method. X-ray spectroscopy techniques on the nanometer scale and high-resolution transmission electron microscopy revealed an orthorhombic structure of nanoporous AgTe with precise lattice constants. First-principles calculations show that the AgTe surface possesses highly active catalytic sites for the HER with an optimized Gibbs free energy change of hydrogen adsorption (-0.005 eV). Our nanoporous AgTe demonstrates exceptional stability and performance for the HER, an overpotential of 27 mV, and a Tafel slope of 33 mV/dec. As a stable catalyst for hydrogen production, AgTe is comparable to platinum-based catalysts and provides a breakthrough for high-performance electrochemical catalysts.
银基纳米材料一直是各种光辅助能源应用的通用构建块;然而,它们表现出较差的电化学催化性能和稳定性,特别是在酸性环境中。在此,我们报告了一种用于析氢反应(HER)的稳定且高性能的碲化银(AgTe)电化学催化剂,它是通过电化学合成方法合成的具有纳米多孔结构的材料。纳米尺度的X射线光谱技术和高分辨率透射电子显微镜揭示了具有精确晶格常数的正交结构纳米多孔AgTe。第一性原理计算表明,AgTe表面具有用于HER的高活性催化位点,氢吸附的吉布斯自由能变化优化为 -0.005 eV。我们的纳米多孔AgTe在HER方面表现出卓越的稳定性和性能,过电位为27 mV,塔菲尔斜率为33 mV/dec。作为一种稳定的制氢催化剂,AgTe可与铂基催化剂相媲美,并为高性能电化学催化剂带来了突破。