Anchoring black phosphorus quantum dots on molybdenum disulfide nanosheets: a 0D/2D nanohybrid with enhanced visible - and NIR - light photoactivity

被引:69
作者
Feng, Rongjuan [1 ]
Lei, Wanying [2 ,3 ]
Sui, Xinyu [2 ,3 ]
Liu, Xinfeng [2 ]
Qi, Xiaoying [2 ]
Tang, Kun [4 ]
Liu, Gang [2 ]
Liu, Minghua [1 ,3 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Nanosyst & Hierarch Fabricat, Beijing 100190, Peoples R China
[2] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Standardizat & Measurement Nanotechno, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Black phosphorus; Molybdenum disulfide; Visible light; Near infrared light; Photocatalysis; TRANSITION-METAL DICHALCOGENIDES; 2-DIMENSIONAL MATERIALS; PHOTOCATALYTIC DEGRADATION; HYDROGEN-PRODUCTION; EVOLUTION; GRAPHENE; MOS2; HETEROSTRUCTURES; NANOPARTICLES; INTERFACE;
D O I
10.1016/j.apcatb.2018.07.052
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photocatalytic solar-to-chemical energy conversion by direct utilizing the full spectrum of sunlight is attracting a great deal of current attention. Black phosphorus (BP), a "rising star" of post-graphene two-dimensional (2D) nanomaterial, holds a unique advantage for this purpose on account of its tunable direct-bandgap for broadband absorption. In this work, for the first time, we anchor BP quantum dots (BPQDs) of similar to 4.2 nm in size onto molybdenum disulfide (MoS2) nanosheets of similar to 3 nm in thickness to create 0D/2D nanohybrids with various BP contents (5-20 wt %) via a facile and cost-effective grinding and sonicating approach. The as-prepared BPQDs/MoS2 nanohybrids show enhanced photocatalytic performance towards methylene orange degradation in water under visible - and near - infrared (NIR) light illumination, respectively. Notably, 10 wt% BPQDs/MoS2 nanohybrids with cyclability achieve the highest NIR - driven photoactivity (3 x 10(-2) min(-1)), which is approximately 13 and 27 folds higher than that of individual BPQDs and MoS2, respectively. We demonstrate that the enhanced light absorption, the type - II band alignment, and the interfacial bonding and the spatial charge separation between well-dispersed BPQDs and MoS2 synergetically enhance the photoactivity and photostability. This study may open avenues to create BP-based heterostructures functional in solar-to-chemical energy conversion and beyond.
引用
收藏
页码:444 / 453
页数:10
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