utilizing NIR light that takes up to about 50% of solar spectrum. One of the reasons is that the low energetic NIR photons only can be utilized to generate free carriers by narrow bandgap semiconductors, up-conversion luminescent material or some localized surface plasmon resonance (LSPR) enhanced noble metal nanomaterials. [3] These materials always suffer from single-wavelength response, poor chemical stability and potentials mismatching. In many cases, the chemical potentials of hole-electrons are not suitable to support the generation of ROS (•OH, •O 2 − and 1 O 2) through individual transition for previous materials. [4] What is more, the NIR-driven photocatalytic mechanism remains to be ambiguous due to the absence of theoretical investigation on the mechanism of NIR absorbance and surface/interface ROS generation kinetics. Therefore, exploiting highefficiency NIR-reactive photocatalyst and comprehensive understanding NIR-driven photocatalytic mechanism are urgent. [5] Compared with traditional semiconductive photocatalysts, metallic photocatalysts with higher carrier density, excellent conductivity, and low-work function open the door for the aimed NIR-responsive photocatalysis. Until now, many theoretical calculations and experimental results have revealed that low-work-function catalysts, such as Ti 3 C 2 T X MXene (Φ = 3.4 eV), halogen-doped monolayer g-C 3 N 4 (Φ = 3.3-4.15 eV), LaCu 0.67 S 1.33 (Φ = 3.5 eV) and MgO (Φ = 3.7 eV), can server as good electron donor and facilitate Realizing near-infrared (NIR) driven photocatalytic reaction is one of the promising strategies to promote the solar energy utilization and photocatalytic efficiencies. However, effective reactive oxygen species (ROS) activation under NIR irradiation remains to be great challenge for nearly all previously reported photocatalysts. Herein, the cubic-phase tungsten nitride (WN) with strong plasmonic NIR absorption and low-work function (≈3.59 eV) is proved to be able to mediate direct ROS activation by both of experimental observation and theoretical simulation. The cubic WN nanocubes (NCs) are synthesized via the hydrothermal-ammonia nitridation process and its NIR-driven photocatalytic properties, including photocatalytic degradation, hydroxylation, and de-esterification, are reported for the first time in this work. The 3D finite element simulation results demonstrate the size dependent and wavelength tuned plasmonic NIR absorption of the WN NCs. The NIR-driven photocatalytic mechanism of WN NCs is proposed based on density functional theory (DFT) calculated electronic structure and facet dependent O 2 (or H 2 O) molecular activation, radicals scavenging test, spin trapped electron paramagnetic resonance measurements, and ultraviolet photoelectronic spectrum (UPS). Overall, the results in this work pave a way for the application of low-workfunction materials as highly reactive NIR photocatalyst.