Photocarrier relaxation pathway in two-dimensional semiconducting transition metal dichalcogenides

• Published in: Nature communications Vol. 5; no. 1; p. 4543
• Main Authors: Kozawa, Daichi, Kumar, Rajeev, Carvalho, Alexandra, Kumar Amara, Kiran, Zhao, Weijie, Wang, Shunfeng, Toh, Minglin, Ribeiro, Ricardo M., Castro Neto, A. H., Matsuda, Kazunari, Eda, Goki
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 29.07.2014; Nature Publishing Group
• Subjects: 140/125; 639/301/119/1000/1018; 639/624/1075/401; Crystals; Humanities and Social Sciences; multidisciplinary; Nesting; Science; Science (multidisciplinary)
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/ncomms5543

Two-dimensional crystals of semiconducting transition metal dichalcogenides absorb a large fraction of incident photons in the visible frequencies despite being atomically thin. It has been suggested that the strong absorption is due to the parallel band or ‘band nesting’ effect and corresponding divergence in the joint density of states. Here, we use photoluminescence excitation spectroscopy to show that the band nesting in mono- and bilayer MX 2 (M=Mo, W and X=S, Se) results in excitation-dependent characteristic relaxation pathways of the photoexcited carriers. Our experimental and simulation results reveal that photoexcited electron–hole pairs in the nesting region spontaneously separate in k -space, relaxing towards immediate band extrema with opposite momentum. These effects imply that the loss of photocarriers due to direct exciton recombination is temporarily suppressed for excitation in resonance with band nesting. Our findings highlight the potential for efficient hot carrier collection using these materials as the absorbers in optoelectronic devices. Two-dimensional semiconducting transition metal dichalcogenides strongly absorb visible light. Kozawa et al. study the photocarrier relaxation in mono- and bilayer MX2 samples and find that loss of photocarriers by direct recombination becomes a second-order process when excitation is in resonance with band nesting.