Baek Minki, Zafar Muhammad, Kim Seongbeen, Kim Do-Heyoung, Jeon Chan-Wook, Lee Jinwoo, Yong Kijung
Surface Chemistry Laboratory of Electronic Materials, Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 790-784, Korea.
School of Chemical Engineering, Chonnam National University, 300 Youngbong-dong, Gwangju, 61186, Korea.
ChemSusChem. 2018 Oct 24;11(20):3679-3688. doi: 10.1002/cssc.201801211. Epub 2018 Sep 13.
Cu(In,Ga)(S,Se) (CIGS) is a promising photocathode material owing to its high absorption coefficient, adjustable band gap, and suitable band edge for the hydrogen evolution reaction (HER). However, most CIGS photocathodes have suffered from instability in applications that require a wide range of pH conditions and have utilized noble metal HER catalysts to achieve a high performance. Thus, improving the durability of the CIGS photocathode under various pH conditions and developing a cost-effective non-noble metal catalyst are critical issues in the photoelectrochemical (PEC) application of this promising photocathode material. Here, we catalyze the CIGS photocathode with Ni-Mo as a non-noble metal to enhance the PEC efficiency, and we employ atomically grown TiO to passivate the CdS/CIGS surface and improve the stability under a wide range of pH conditions. Our Ni-Mo alloy exhibits the best HER catalytic activity among reported earth-abundant HER catalysts in both acidic and alkaline solutions. The Ni-Mo/CdS/CIGS photocathode yields an onset potential of 0.5 V (vs. RHE) and a short-circuit photocurrent density as high as 15-25 mA cm under various pH conditions ranging from 0.4 to 14, which is highly comparable to that of Pt/CdS/CIGS. Furthermore, the passivation of CdS/CIGS with a thin TiO layer, obtained by atomic layer deposition, effectively prevents the photocorrosion of CdS and the dissolution of the Mo back contact, which are the main causes of the degradation of the photocathode. The optimized Ni-Mo/TiO /CdS/CIGS photocathode produces a stable photocurrent density at 0 V for 100 minutes except under strong alkaline conditions. The current work presents a very useful method to improve the efficiency and durability of the CIGS photocathodes with an earth-abundant metal catalyst, which completely replaces Pt.
铜铟镓硫硒(CIGS)因其高吸收系数、可调节的带隙以及适合析氢反应(HER)的带边,是一种很有前景的光阴极材料。然而,大多数CIGS光阴极在需要广泛pH条件的应用中存在稳定性问题,并且为了实现高性能而使用了贵金属HER催化剂。因此,提高CIGS光阴极在各种pH条件下的耐久性以及开发具有成本效益的非贵金属催化剂是这种有前景的光阴极材料在光电化学(PEC)应用中的关键问题。在此,我们用镍钼作为非贵金属催化CIGS光阴极以提高PEC效率,并且我们采用原子生长的TiO来钝化CdS/CIGS表面并在广泛的pH条件下提高稳定性。我们的镍钼合金在酸性和碱性溶液中,在所报道的储量丰富的HER催化剂中表现出最佳的HER催化活性。Ni-Mo/CdS/CIGS光阴极在0.4至14的各种pH条件下产生0.5 V(相对于可逆氢电极,RHE)的起始电位和高达15 - 25 mA cm的短路光电流密度,这与Pt/CdS/CIGS的高度相当。此外,通过原子层沉积获得的薄TiO层对CdS/CIGS进行钝化,有效地防止了CdS的光腐蚀和Mo背接触的溶解,这是光阴极降解的主要原因。优化后的Ni-Mo/TiO /CdS/CIGS光阴极除了在强碱性条件下,在0 V时能产生100分钟的稳定光电流密度。当前的工作提出了一种非常有用的方法,用储量丰富的金属催化剂提高CIGS光阴极的效率和耐久性,该催化剂完全替代了Pt。